Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:70097867-70098092 | Common:1; Rare:51 | ||||
chr15:70763426-70763789 | Common:2; Rare:120 | ||||
chr15:70892495-70892868 | Common:1; Rare:83 | ||||
chr15:72118165-72118434 | Common:2; Rare:89 | ||||
chr15:72231107-72231520 | Common:3; Rare:132 | ||||
chr15:72231589-72231643 | Rare:9 | ||||
chr15:72375958-72376103 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686171-72686225 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73633238-73633596 | Common:2; Rare:141 | ||||
chr15:73994587-73994716 | Rare:20 | ||||
chr15:74461106-74461314 | Rare:65 | ||||
chr15:74540962-74541268 | Common:3; Rare:107 | ||||
chr15:74615556-74615898 | Common:4; Rare:107 | ||||
chr15:74695987-74696098 | Rare:34 | ||||
chr15:74873299-74873481 | Common:5; Rare:56 |