Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:74540966-74541283 | Common:4; Rare:112 | ||||
chr15:74615597-74615898 | Common:4; Rare:98 | ||||
chr15:74695963-74696069 | Rare:37 | ||||
chr15:74843110-74843318 | Common:1; Rare:64 | ||||
chr15:74873307-74873461 | Common:5; Rare:49 | ||||
chr15:74889965-74890076 | Rare:48; Clinvar (pathogenic):1 | ||||
chr15:74906789-74906871 | Rare:39 | ||||
chr15:74937990-74938272 | Common:2; Rare:95 | ||||
chr15:75023467-75023611 | Common:1; Rare:31 | ||||
chr15:75335967-75336114 | Common:1; Rare:69 | ||||
chr15:75625612-75625875 | Common:2; Rare:63 | ||||
chr15:75640115-75640399 | Common:1; Rare:97 | ||||
chr15:75647859-75647920 | Rare:10 | ||||
chr15:75843547-75843648 | Rare:47 | ||||
chr15:75903810-75903985 | Rare:74 |