Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:241273880-241274029 | Rare:30 | ||||
chr2:241570031-241570200 | Rare:66 | ||||
chr2:241687821-241688033 | Rare:54 | ||||
chr20:327701-327726 | Rare:6 | ||||
chr20:1327108-1327175 | Common:1; Rare:22 | ||||
chr20:1875859-1875981 | Common:3; Rare:34 | ||||
chr20:3934050-3934337 | Rare:64 | ||||
chr20:10645422-10645640 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr20:10666453-10666684 | Rare:45 | ||||
chr20:13072083-13072363 | Rare:52 | ||||
chr20:17973207-17973238 | Rare:11 | ||||
chr20:18793969-18794102 | Rare:45 | ||||
chr20:19757372-19757625 | Common:3; Rare:55 | ||||
chr20:19757945-19758276 | Common:4; Rare:114 | ||||
chr20:23047735-23048241 | Common:3; Rare:192; Clinvar:3; Clinvar (benign):4 |