| ID: 132090454 | Neanderthal introgressed variant-containing enhancer experimental_46971 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12691457..12691626) | | |
| ID: 130060301 | ATAC-STARR-seq lymphoblastoid active region 11739 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12939979..12940188) | | |
| ID: 130060300 | ATAC-STARR-seq lymphoblastoid active region 11738 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12859672..12860011) | | |
| ID: 130060299 | ATAC-STARR-seq lymphoblastoid active region 11737 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12815809..12815898) | | |
| ID: 130060298 | ATAC-STARR-seq lymphoblastoid silent region 8206 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12789425..12789774) | | |
| ID: 130060297 | ATAC-STARR-seq lymphoblastoid active region 11736 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12431136..12431585) | | |
| ID: 129663980 | ReSE screen-validated silencer GRCh37_chr17:12287658-12287861 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12384341..12384544) | | |
| ID: 127885821 | H3K27ac hESC enhancer GRCh37_chr17:12920660-12921160 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (13017343..13017843) | | |
| ID: 127885820 | H3K27ac hESC enhancer GRCh37_chr17:12591959-12592459 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12688642..12689142) | | |
| ID: 127885819 | H3K27ac hESC enhancer GRCh37_chr17:12591458-12591958 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12688141..12688641) | | |
| ID: 127885818 | H3K27ac hESC enhancer GRCh37_chr17:12540895-12541394 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12637578..12638077) | | |
| ID: 127885817 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:12358360-12358972 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12455043..12455655) | | |
| ID: 127885816 | OCT4-NANOG hESC enhancer GRCh37_chr17:12125284-12125872 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12221967..12222555) | | |
| ID: 126862508 | BRD4-independent group 4 enhancer GRCh37_chr17:12533784-12534983 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12630467..12631666) | | |
| ID: 125177421 | Sharpr-MPRA regulatory region 8598 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12977272..12977566) | | |
| ID: 125177420 | Sharpr-MPRA regulatory region 9419 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12545932..12546226) | | |
| ID: 105371540 | uncharacterized LOC105371540 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12591752..12605960, complement) | | |
| ID: 103156999 | dynein light chain Tctex-type 1 pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12115519..12116239) | | |
| ID: 101928418 | MYOCD antisense RNA 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12671862..12706135, complement) | | |
| ID: 100616494 | microRNA 1269b [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12917268..12917342, complement) | | |