| ID: 127884480 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr16:72319061-72319706 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72285162..72285807) | | |
| ID: 127884479 | H3K4me1 hESC enhancer GRCh37_chr16:72171124-72171624 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72137225..72137725) | | |
| ID: 127884478 | H3K4me1 hESC enhancer GRCh37_chr16:72163923-72164424 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72130024..72130525) | | |
| ID: 127884477 | NANOG hESC enhancer GRCh37_chr16:72162293-72163093 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72128394..72129194) | | |
| ID: 127884476 | H3K27ac hESC enhancer GRCh37_chr16:72159455-72159956 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72125556..72126057) | | |
| ID: 127884475 | H3K4me1 hESC enhancer GRCh37_chr16:72132901-72133401 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72099002..72099502) | | |
| ID: 126862392 | MED14-independent group 3 enhancer GRCh37_chr16:72257113-72258312 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72223214..72224413) | | |
| ID: 126862391 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:72141414-72142613 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72107515..72108714) | | |
| ID: 124903720 | uncharacterized LOC124903720 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72266838..72286891) | | |
| ID: 110120573 | VISTA enhancer hs22 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72220667..72221926) | | |
| ID: 105371341 | uncharacterized LOC105371341 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72203661..72209634) | | |
| ID: 101927957 | long intergenic non-protein coding RNA 1572 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72280902..72664970, complement) | | |
| ID: 390739 | MYC binding protein pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72278241..72280766) | | |
| ID: 83449 | polyamine modulated factor 1 binding protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72116657..72249949, complement) | SPGF31, STAP | 618085 |
| ID: 9785 | DEAH-box helicase 38 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72093847..72112912) | DDX38, PRP16, PRPF16, RP84 | 605584 |