Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:49414830-49415143 | Common:2; Rare:76 | ||||
chr17:49788576-49788718 | Common:1; Rare:42 | ||||
chr17:50373168-50373246 | Common:3; Rare:31 | ||||
chr17:50634627-50634958 | Common:3; Rare:71 | ||||
chr17:50719469-50719661 | Rare:74 | ||||
chr17:51260361-51260587 | Common:3; Rare:102 | ||||
chr17:54968638-54968765 | Common:3; Rare:61 | ||||
chr17:56914016-56914186 | Rare:46 | ||||
chr17:57850002-57850274 | Common:1; Rare:89 | ||||
chr17:58007223-58007347 | Rare:53 | ||||
chr17:58352140-58352473 | Common:6; Rare:130 | ||||
chr17:58692541-58692637 | Common:1; Rare:49; Clinvar (benign):14 | ||||
chr17:59106715-59106994 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155150-59155340 | Common:1; Rare:50 | ||||
chr17:59155557-59155774 | Rare:61 |