Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97633434-97633618 | Common:2; Rare:45 | ||||
chr10:98446878-98447043 | Rare:47 | ||||
chr10:99430622-99430936 | Common:3; Rare:70 | ||||
chr10:99659244-99659554 | Common:1; Rare:78 | ||||
chr10:99732070-99732329 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185938-100186194 | Rare:100 | ||||
chr10:100267606-100267733 | Common:3; Rare:41 | ||||
chr10:100286582-100286721 | Common:4; Rare:81 | ||||
chr10:100346911-100347424 | Common:3; Rare:116 | ||||
chr10:100912730-100913023 | Common:1; Rare:93 | ||||
chr10:100913328-100913471 | Rare:35 | ||||
chr10:100987228-100987573 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031090-101031275 | Common:1; Rare:46 | ||||
chr10:101229427-101229573 | Rare:28 | ||||
chr10:101588205-101588347 | Rare:57 |