Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48944757-48944884 | Common:1; Rare:48 | ||||
chr17:49414833-49415120 | Common:1; Rare:68 | ||||
chr17:49788462-49788731 | Common:1; Rare:85 | ||||
chr17:50274267-50274540 | Common:3; Rare:69 | ||||
chr17:50345897-50346131 | Common:4; Rare:79 | ||||
chr17:50373160-50373259 | Common:3; Rare:43 | ||||
chr17:50719489-50719645 | Rare:59 | ||||
chr17:51260151-51260577 | Common:3; Rare:151 | ||||
chr17:54968638-54968775 | Common:3; Rare:66 | ||||
chr17:57850006-57850274 | Common:1; Rare:86 | ||||
chr17:58007146-58007380 | Common:1; Rare:112 | ||||
chr17:58219226-58219372 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
chr17:58692357-58692668 | Common:2; Rare:129; Clinvar:10; Clinvar (benign):20 | ||||
chr17:59106707-59106966 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155146-59155499 | Common:2; Rare:80 |