Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99430602-99430937 | Common:3; Rare:77 | ||||
chr10:99659265-99659574 | Common:2; Rare:77 | ||||
chr10:99732041-99732309 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100229528-100229660 | Rare:50 | ||||
chr10:100347156-100347532 | Common:4; Rare:88 | ||||
chr10:100987405-100987573 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031102-101031295 | Common:1; Rare:45 | ||||
chr10:101588129-101588328 | Rare:85 | ||||
chr10:102120432-102120665 | Common:1; Rare:83 | ||||
chr10:102714267-102714641 | Common:2; Rare:125 | ||||
chr10:102918425-102918550 | Rare:39 | ||||
chr10:103396435-103396719 | Rare:99 | ||||
chr10:104338416-104338528 | Rare:30 | ||||
chr10:110006016-110006063 | Common:1; Rare:14 | ||||
chr10:110007712-110008015 | Rare:86 |