Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:68817613-68817684 | Rare:23 | ||||
chr15:68930343-68930589 | Common:3; Rare:76 | ||||
chr15:69160407-69160639 | Common:2; Rare:70 | ||||
chr15:69298761-69298986 | Common:3; Rare:46 | ||||
chr15:69414208-69414453 | Rare:85 | ||||
chr15:69452701-69453020 | Common:5; Rare:132 | ||||
chr15:70853205-70853445 | Common:1; Rare:41 | ||||
chr15:70892381-70892640 | Common:1; Rare:62 | ||||
chr15:72118167-72118434 | Common:2; Rare:88 | ||||
chr15:72231109-72231520 | Common:3; Rare:130 | ||||
chr15:72272520-72272731 | Rare:63 | ||||
chr15:72375932-72376129 | Common:2; Rare:81; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr15:72474215-72474351 | Rare:46 | ||||
chr15:72686135-72686220 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73633184-73633595 | Common:2; Rare:162 |