Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:65611110-65611365 | Common:1; Rare:80 | ||||
chr15:66386707-66386940 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
chr15:66504786-66505140 | Common:1; Rare:135 | ||||
chr15:67254615-67254818 | Common:1; Rare:76 | ||||
chr15:68820794-68821090 | Rare:82 | ||||
chr15:69414209-69414366 | Rare:44 | ||||
chr15:69452688-69452896 | Common:4; Rare:95 | ||||
chr15:72118168-72118425 | Common:2; Rare:80 | ||||
chr15:72231114-72231516 | Common:3; Rare:126 | ||||
chr15:72375958-72376092 | Common:2; Rare:59; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:73684082-73684407 | Rare:91 | ||||
chr15:73926290-73926471 | Rare:48 | ||||
chr15:73994600-73994788 | Rare:40 | ||||
chr15:74461100-74461298 | Rare:63 | ||||
chr15:74615559-74615884 | Common:4; Rare:103 |