Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:70892381-70892760 | Common:1; Rare:85 | ||||
chr15:72118168-72118434 | Common:2; Rare:87 | ||||
chr15:72231102-72231664 | Common:6; Rare:171 | ||||
chr15:72375968-72376117 | Common:1; Rare:64; Clinvar:5; Clinvar (pathogenic):2 | ||||
chr15:72783696-72783816 | Common:2; Rare:51 | ||||
chr15:73926272-73926471 | Rare:51 | ||||
chr15:73994587-73994790 | Rare:44 | ||||
chr15:74461106-74461298 | Rare:62 | ||||
chr15:74695987-74696049 | Rare:20 | ||||
chr15:74873307-74873451 | Common:5; Rare:48 | ||||
chr15:74889958-74890064 | Rare:42 | ||||
chr15:74938010-74938243 | Common:2; Rare:84 | ||||
chr15:75368585-75368766 | Rare:51 | ||||
chr15:75451682-75451983 | Common:1; Rare:80 | ||||
chr15:75455790-75455967 | Rare:58 |