| ID: 127401904 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:170256304-170256981 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169335153..169335830) | | |
| ID: 127401903 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:170232766-170233314 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169311615..169312163) | | |
| ID: 127401902 | H3K4me1 hESC enhancer GRCh37_chr4:170162265-170162765 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169241114..169241614) | | |
| ID: 127401901 | H3K4me1 hESC enhancer GRCh37_chr4:170161764-170162264 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169240613..169241113) | | |
| ID: 127401900 | OCT4-NANOG hESC enhancer GRCh37_chr4:170150634-170151313 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169229483..169230162) | | |
| ID: 127401899 | H3K27ac hESC enhancer GRCh37_chr4:169995185-169995684 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169074034..169074533) | | |
| ID: 127401898 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:169991001-169991955 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169069850..169070804) | | |
| ID: 126807218 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:170172321-170173520 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169251170..169252369) | | |
| ID: 126807217 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:170146248-170147447 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169225097..169226296) | | |
| ID: 123493236 | Sharpr-MPRA regulatory region 2565 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169249518..169249812) | | |
| ID: 105377529 | uncharacterized LOC105377529 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169275264..169331178, complement) | | |
| ID: 105377527 | uncharacterized LOC105377527 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169059056..169074273, complement) | | |
| ID: 100270907 | ribosomal protein L6 pseudogene 12 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169166254..169167152) | RPL6_11_535 | |
| ID: 57630 | SH3 domain containing ring finger 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169094259..169270956, complement) | POSH, RNF142, SH3MD2 | 618642 |