Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97633489-97633604 | Rare:28 | ||||
chr10:98134816-98134902 | Rare:27 | ||||
chr10:99430563-99430930 | Common:4; Rare:86 | ||||
chr10:99659227-99659571 | Common:2; Rare:91 | ||||
chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185765-100186198 | Rare:144 | ||||
chr10:100229553-100229631 | Rare:25 | ||||
chr10:100346921-100347531 | Common:4; Rare:145 | ||||
chr10:100912751-100913030 | Common:1; Rare:85 | ||||
chr10:100969280-100969530 | Common:3; Rare:61 | ||||
chr10:100987222-100987590 | Common:1; Rare:135; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031120-101031275 | Common:1; Rare:35 | ||||
chr10:101588166-101588357 | Rare:81; Clinvar:1 | ||||
chr10:101818141-101818196 | Rare:13 | ||||
chr10:101818290-101818770 | Common:1; Rare:132 |