Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:69452799-69453020 | Common:3; Rare:99 | ||||
chr15:70853894-70854289 | Common:1; Rare:113 | ||||
chr15:70892376-70892855 | Common:1; Rare:107 | ||||
chr15:72118015-72118432 | Common:3; Rare:145 | ||||
chr15:72230219-72230573 | Common:3; Rare:98 | ||||
chr15:72231107-72231415 | Common:2; Rare:97 | ||||
chr15:72272524-72272604 | Rare:30 | ||||
chr15:72375958-72376129 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72474210-72474532 | Rare:108 | ||||
chr15:73926294-73926482 | Rare:50 | ||||
chr15:73994595-73994801 | Rare:44 | ||||
chr15:74367644-74367883 | Rare:37 | ||||
chr15:74461106-74461329 | Rare:66 | ||||
chr15:74615678-74615898 | Common:3; Rare:68 | ||||
chr15:74628652-74628994 | Rare:83 |