| ID: 127273135 | NANOG hESC enhancer GRCh37_chr2:40545966-40546467 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40318826..40319327) | | |
| ID: 127273134 | OCT4-NANOG hESC enhancer GRCh37_chr2:40469400-40469950 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40242260..40242810) | | |
| ID: 127273133 | OCT4-NANOG hESC enhancer GRCh37_chr2:40437586-40438180 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40210446..40211040) | | |
| ID: 127273132 | OCT4-NANOG hESC enhancer GRCh37_chr2:40371191-40371761 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40144051..40144621) | | |
| ID: 127273131 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:40240930-40241498 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40013790..40014358) | | |
| ID: 127273130 | H3K4me1 hESC enhancer GRCh37_chr2:40147641-40148300 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39920501..39921160) | | |
| ID: 126806199 | MED14-independent group 3 enhancer GRCh37_chr2:40661639-40662838 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40434499..40435698) | | |
| ID: 126806198 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:40165083-40166282 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39937943..39939142) | | |
| ID: 126806197 | MED14-independent group 3 enhancer GRCh37_chr2:40128919-40130118 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39901779..39902978) | | |
| ID: 124905995 | peptidyl-prolyl cis-trans isomerase NIMA-interacting 4-like [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40375939..40401566, complement) | | |
| ID: 120961747 | Sharpr-MPRA regulatory region 14225 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40401929..40402223) | | |
| ID: 120961746 | Sharpr-MPRA regulatory region 6978 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40096409..40096703) | | |
| ID: 112268436 | uncharacterized LOC112268436 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39901937..39904495) | | |
| ID: 105374475 | uncharacterized LOC105374475 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40632909..40643685, complement) | | |
| ID: 105374473 | uncharacterized LOC105374473 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40617528..40621154, complement) | | |
| ID: 101929667 | uncharacterized LOC101929667 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40511922..40558453) | | |
| ID: 100419512 | zinc finger protein 19 pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39929194..39929974) | | |
| ID: 100128590 | SLC8A1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (39917634..40255209) | | |
| ID: 6546 | solute carrier family 8 member A1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (40097270..40512435, complement) | NCX1 | 182305 |