| ID: 130060846 | ATAC-STARR-seq lymphoblastoid silent region 8497 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41682019..41682098) | | |
| ID: 130060845 | ATAC-STARR-seq lymphoblastoid active region 12170 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41678724..41678953) | | |
| ID: 130060844 | ATAC-STARR-seq lymphoblastoid active region 12169 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41667261..41667490) | | |
| ID: 130060843 | ATAC-STARR-seq lymphoblastoid active region 12168 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41666261..41666390) | | |
| ID: 130060842 | ATAC-STARR-seq lymphoblastoid active region 12166 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41648541..41648650) | | |
| ID: 127886854 | OCT4-NANOG hESC enhancer GRCh37_chr17:39864421-39864948 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41708169..41708696) | | |
| ID: 127886853 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39861304-39862096 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41705052..41705844) | | |
| ID: 127886852 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39845747-39846655 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41689480..41690403) | | |
| ID: 127886851 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:39844838-39845746 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41688586..41689494) | | |
| ID: 127886850 | H3K4me1 hESC enhancer GRCh37_chr17:39821965-39822482 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41665713..41666230) | | |
| ID: 127886849 | H3K4me1 hESC enhancer GRCh37_chr17:39821445-39821964 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41665193..41665712) | | |
| ID: 127886848 | H3K4me1 hESC enhancer GRCh37_chr17:39816537-39817036 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41660285..41660784) | | |
| ID: 127886847 | H3K4me1 hESC enhancer GRCh37_chr17:39810501-39811197 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41654249..41654945) | | |
| ID: 127886846 | H3K4me1 hESC enhancer GRCh37_chr17:39809802-39810500 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41653550..41654248) | | |
| ID: 127886845 | H3K4me1 hESC enhancer GRCh37_chr17:39803627-39804502 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41647375..41648250) | | |
| ID: 125177475 | Sharpr-MPRA regulatory region 1334 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41717457..41717751) | | |
| ID: 124904004 | uncharacterized LOC124904004 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41647277..41655134, complement) | | |
| ID: 106480768 | RNA, 5S ribosomal pseudogene 442 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41718154..41718243) | RN5S442 | |
| ID: 284116 | keratin 42, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41626327..41640199, complement) | | |
| ID: 10209 | eukaryotic translation initiation factor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41688885..41692668) | A121, EIF-1A, ISO1, SUI1, EIF1 | 619901 |