| ID: 127821482 | H3K4me1 hESC enhancer GRCh37_chr11:65210919-65211744 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65443448..65444273) | | |
| ID: 127821480 | H3K27ac-H3K4me1 hESC enhancers GRCh37_chr11:65189569-65190154 and GRCh37_chr11:65190155-65190740 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65422098..65423269) | | |
| ID: 127821479 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:65187227-65187812 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65419756..65420343) | | |
| ID: 127821478 | H3K4me1 hESC enhancer GRCh37_chr11:65171719-65172218 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65404248..65404747) | | |
| ID: 127821477 | H3K4me1 hESC enhancer GRCh37_chr11:65167805-65168690 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65400334..65401219) | | |
| ID: 127821476 | H3K4me1 hESC enhancer GRCh37_chr11:65160023-65160609 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65392552..65393138) | | |
| ID: 127821475 | H3K4me1 hESC enhancer GRCh37_chr11:65156452-65157086 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65388981..65389615) | | |
| ID: 127821474 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:65153824-65154412 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65386353..65387023) | | |
| ID: 127821473 | H3K4me1 hESC enhancer GRCh37_chr11:65144096-65144596 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65376625..65377125) | | |
| ID: 124500669 | Sharpr-MPRA regulatory region 4367 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65429958..65430252) | | |
| ID: 124500668 | Sharpr-MPRA regulatory region 10780 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65383340..65384072) | | |
| ID: 124500667 | Sharpr-MPRA regulatory region 3865 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65363798..65364092) | | |
| ID: 116216143 | MED14-independent group 3 enhancer GRCh37_chr11:65188260-65189459 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65420789..65422097) | | |
| ID: 116216142 | CRISPRi-validated cis-regulatory element chr11.3233 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65418000..65419496) | | |
| ID: 112081410 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr11:65149420-65150619 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65381755..65383148) | | |
| ID: 693197 | microRNA 612 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65444458..65444557) | MIRN612, hsa-mir-612 | |
| ID: 283131 | nuclear paraspeckle assembly transcript 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65422798..65445540) | LINC00084, NCRNA00084, TP53LC15, TncRNA, VINC | 612769 |
| ID: 283130 | solute carrier family 25 member 45 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65375192..65383701, complement) | | 610825 |
| ID: 220359 | tigger transposable element derived 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65354751..65357613) | | 619084 |
| ID: 83786 | FERM domain containing 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65368026..65426526) | FKSG44, iTAP | 618337 |