Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40425989-40426147 | Common:1; Rare:46 | ||||
chr19:40465811-40466112 | Common:3; Rare:87 | ||||
chr19:40605997-40606300 | Common:3; Rare:73; Clinvar (benign):2 | ||||
chr19:40611957-40612127 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):4 | ||||
chr19:40715074-40715183 | Rare:29 | ||||
chr19:40716880-40717114 | Common:1; Rare:73 | ||||
chr19:40717728-40717901 | Rare:46 | ||||
chr19:40798916-40799248 | Common:6; Rare:124 | ||||
chr19:41218858-41219003 | Common:2; Rare:33 | ||||
chr19:41262326-41262566 | Rare:45 | ||||
chr19:41310041-41310290 | Rare:94 | ||||
chr19:41353797-41354086 | Common:2; Rare:96 | ||||
chr19:41898061-41898342 | Common:1; Rare:64 | ||||
chr19:41905755-41905985 | Common:1; Rare:68 | ||||
chr19:42075817-42076191 | Rare:102 |