Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102399499-102399880 | Rare:160; Clinvar (benign):2 | ||||
chr10:102422150-102422490 | Rare:94 | ||||
chr10:102449705-102449919 | Common:3; Rare:107 | ||||
chr10:102451459-102451742 | Rare:172 | ||||
chr10:102507385-102507825 | Common:3; Rare:154 | ||||
chr10:102592426-102593680 | Common:3; Rare:375; Clinvar:3; Clinvar (benign):4 | ||||
chr10:102634669-102635069 | Rare:155 | ||||
chr10:102642055-102642571 | Common:3; Rare:295 | ||||
chr10:102642769-102643158 | Common:3; Rare:137 | ||||
chr10:102643095-102643499 | Common:7; Rare:162 | ||||
chr10:102643470-102643802 | Common:2; Rare:158 | ||||
chr10:102645499-102645752 | Common:2; Rare:115 | ||||
chr10:102710586-102711050 | Common:3; Rare:216 | ||||
chr10:102712748-102713239 | Common:24; Rare:137 | ||||
chr10:102713269-102713686 | Rare:79 |