ID: 127883137 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11290798-11291307 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11196941..11197450) | | |
ID: 127883136 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11276367-11277253 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11182510..11183491) | | |
ID: 127883135 | H3K4me1 hESC enhancer GRCh37_chr16:11275481-11276366 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11181624..11182509) | | |
ID: 127883134 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11268031-11268544 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11174174..11174687) | | |
ID: 127883133 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11238795-11239462 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11144938..11145605) | | |
ID: 127883132 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11235162-11235740 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11141305..11141883) | | |
ID: 127883131 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11234584-11235161 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11140727..11141304) | | |
ID: 127883130 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11234005-11234583 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11140148..11140726) | | |
ID: 127883129 | H3K4me1 hESC enhancer GRCh37_chr16:11144766-11145343 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11050909..11051486) | | |
ID: 127883128 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:11144189-11144765 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11050332..11050908) | | |
ID: 127883127 | NANOG hESC enhancer GRCh37_chr16:11101530-11102234 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11007673..11008377) | | |
ID: 127883126 | H3K4me1 hESC enhancer GRCh37_chr16:11074261-11074760 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10980404..10980903) | | |
ID: 127883125 | H3K4me1 hESC enhancer GRCh37_chr16:11073759-11074260 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10979902..10980403) | | |
ID: 126862287 | BRD4-independent group 4 enhancer GRCh37_chr16:10964767-10965966 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10870910..10872109) | | |
ID: 125146407 | Sharpr-MPRA regulatory region 10204 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11016712..11017006) | | |
ID: 125146406 | Sharpr-MPRA regulatory region 12638 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (10971532..10971826) | | |
ID: 124907823 | uncharacterized LOC124907823 [Homo sapiens (human)] | | | |
ID: 121530617 | Sharpr-MPRA regulatory region 12604 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11113032..11113326) | | |
ID: 105371081 | uncharacterized LOC105371081 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11129371..11135050, complement) | | |
ID: 642451 | ribosomal protein L7 pseudogene 46 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11026961..11028561) | RPL7_26_1472 | |