| ID: 127887156 | OCT4-NANOG hESC enhancer GRCh37_chr17:45416653-45417154 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47339287..47339788) | | |
| ID: 127887155 | H3K4me1 hESC enhancer GRCh37_chr17:45369753-45370253 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47292387..47292887) | | |
| ID: 127887154 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:45353259-45353806 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47275893..47276440) | | |
| ID: 127887153 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:45315603-45316539 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47238237..47239173) | | |
| ID: 127887152 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:45314666-45315602 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47237300..47238236) | | |
| ID: 125177495 | Sharpr-MPRA regulatory region 1659 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47362223..47362517) | | |
| ID: 125177494 | Sharpr-MPRA regulatory region 629 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47275303..47275597) | | |
| ID: 121587599 | Sharpr-MPRA regulatory region 4923 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47280483..47281111) | | |
| ID: 112533645 | Sharpr-MPRA regulatory region 4395 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47288543..47288837) | | |
| ID: 110121475 | VISTA enhancer hs2033 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47291162..47292148) | | |
| ID: 107985029 | uncharacterized LOC107985029 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47279525..47280262, complement) | | |
| ID: 106480363 | RNA, U7 small nuclear 186 pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47259358..47259420, complement) | | |
| ID: 102724508 | EFCAB13 divergent transcript [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47303443..47323901, complement) | THCAT158 | |
| ID: 124989 | EF-hand calcium binding domain 13 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47323955..47441312) | C17orf57 | |
| ID: 3690 | integrin subunit beta 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47253827..47313743) | BDPLT16, BDPLT2, BDPLT24, CD61, GP3A, GPIIIa, GT, GT2 | 173470 |