| ID: 127824677 | NANOG hESC enhancer GRCh37_chr12:85397904-85398436 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (85004125..85004657) | | |
| ID: 127824676 | H3K27ac hESC enhancer GRCh37_chr12:85306793-85307339 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84913014..84913560) | | |
| ID: 127824675 | H3K27ac hESC enhancer GRCh37_chr12:85306245-85306792 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84912466..84913013) | | |
| ID: 127824674 | H3K27ac hESC enhancer GRCh37_chr12:85305148-85305696 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84911369..84911917) | | |
| ID: 127824673 | OCT4-NANOG hESC enhancer GRCh37_chr12:85198877-85199735 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84805098..84805956) | | |
| ID: 127824672 | NANOG hESC enhancer GRCh37_chr12:85117712-85118213 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84723933..84724434) | | |
| ID: 127824671 | NANOG hESC enhancer GRCh37_chr12:85083456-85083957 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84689677..84690178) | | |
| ID: 124903121 | uncharacterized LOC124903121 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84893873..84894026, complement) | | |
| ID: 112163634 | Sharpr-MPRA regulatory region 14945 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (85016430..85016724) | | |
| ID: 105369875 | uncharacterized LOC105369875 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84492397..84508906, complement) | | |
| ID: 102724680 | uncharacterized LOC102724680 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84912837..84992657) | | |
| ID: 100128335 | WD repeat domain 12 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84448433..84450048, complement) | | |
| ID: 144448 | tetraspanin 19 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (85014317..85036277, complement) | | |
| ID: 55117 | solute carrier family 6 member 15 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (84859491..84912799, complement) | NTT73, SBAT1, V7-3, hv7-3 | 607971 |