Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:23647847-23647970 | Rare:34 | ||||
chr15:23687269-23687494 | Common:1; Rare:74 | ||||
chr15:24823717-24823798 | Rare:13 | ||||
chr15:24856422-24856594 | Common:3; Rare:49 | ||||
chr15:24954765-24955066 | Common:1; Rare:127 | ||||
chr15:24955262-24955479 | Rare:60 | ||||
chr15:25438494-25438522 | Rare:10 | ||||
chr15:25438529-25438610 | Rare:20 | ||||
chr15:25438916-25439227 | Common:3; Rare:105 | ||||
chr15:26767204-26767391 | Common:2; Rare:35 | ||||
chr15:26772930-26773184 | Common:1; Rare:87; Clinvar (benign):1 | ||||
chr15:28886110-28886244 | Common:1; Rare:36 | ||||
chr15:29269706-29269949 | Common:2; Rare:121 | ||||
chr15:29822359-29822631 | Common:2; Rare:112 | ||||
chr15:30903686-30903943 | Common:2; Rare:63 |