ID: 127885661 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7460817-7461610 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7557500..7558293) | | |
ID: 127885660 | H3K4me1 hESC enhancer GRCh37_chr17:7458208-7458708 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7554891..7555391) | | |
ID: 127885659 | H3K27ac hESC enhancer GRCh37_chr17:7387892-7388885 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7484573..7485566) | | |
ID: 127885658 | OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7386897-7387891 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7483578..7484572) | | |
ID: 127885657 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7368787-7369309 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7465468..7465990) | | |
ID: 126862482 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:7414586-7415785 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7511267..7512466) | | |
ID: 126862481 | BRD4-independent group 4 enhancer GRCh37_chr17:7405086-7406285 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7501767..7502966) | | |
ID: 643664 | solute carrier family 35 member G6 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7481446..7483496) | AMAC1L3, TMEM21B | |
ID: 407977 | TNFSF12-TNFSF13 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7549058..7561601) | TWE-PRIL | |
ID: 57659 | zinc finger and BTB domain containing 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7459378..7484249, complement) | KAISO-L1, ZNF903 | 612308 |
ID: 8742 | TNF superfamily member 12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7549058..7557881) | APO3L, DR3LG, TNLG4A, TWEAK | 602695 |
ID: 8741 | TNF superfamily member 13 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7558282..7561601) | APRIL, CD256, TALL-2, TALL2, TNLG7B, TRDL-1, UNQ383/PRO715, ZTNF2 | 604472 |
ID: 5430 | RNA polymerase II subunit A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7484366..7514616) | NEDHIB, POLR2, POLRA, RPB1, RPBh1, RPO2, RPOL2, RpIILS, hRPB220, hsRPB1 | 180660 |