| ID: 127885280 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:475469-476353 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (572229..573113) | | |
| ID: 127885279 | H3K27ac hESC enhancer GRCh37_chr17:423721-424222 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (520481..520982) | | |
| ID: 127885278 | OCT4-NANOG hESC enhancer GRCh37_chr17:276928-277621 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (427137..427830) | | |
| ID: 126862458 | BRD4-independent group 4 enhancer GRCh37_chr17:560426-561625 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (657186..658385) | | |
| ID: 126862457 | BRD4-independent group 4 enhancer GRCh37_chr17:504328-505527 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (601088..602287) | | |
| ID: 126862456 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:463241-464440 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (560001..561200) | | |
| ID: 125177400 | Sharpr-MPRA regulatory region 15051 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (676369..676663) | | |
| ID: 125177399 | Sharpr-MPRA regulatory region 8461 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (673229..673523) | | |
| ID: 124903893 | uncharacterized LOC124903893 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (722072..732380, complement) | | |
| ID: 124903891 | uncharacterized LOC124903891 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (555884..556340) | | |
| ID: 124903890 | uncharacterized LOC124903890 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (522737..551353) | | |
| ID: 121848002 | Sharpr-MPRA regulatory region 11717 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (729809..730103) | | |
| ID: 100128140 | ribosomal protein S4X pseudogene 17 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (656732..657596, complement) | RPS4P17, RPS4X_7_1505 | |
| ID: 359845 | refilin B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (439978..445940, complement) | CFM1, FAM101B | 615928 |
| ID: 79850 | TLC domain containing 3A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (732596..742968) | CT120, FAM57A | 611627 |
| ID: 55275 | VPS53 subunit of GARP complex [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (508668..714839, complement) | HCCS1, PCH2E, hVps53L, pp13624 | 615850 |