Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633956-49634084 | Common:1; Rare:54; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:73245966-73246108 | Common:2; Rare:60 | ||||
chr15:51094632-51094982 | Common:8; Rare:94 | ||||
chr15:71165480-71165498 | Rare:1 | ||||
chr15:73927695-73927851 | Common:1; Rare:46 | ||||
chr15:82750424-82750591 | Common:2; Rare:43 | ||||
chr16:11841782-11841958 | Common:2; Rare:67 | ||||
chr17:1479432-1479652 | Common:2; Rare:89 | ||||
chr17:48546455-48546683 | Rare:42 | ||||
chr17:50197961-50198175 | Common:3; Rare:56; Clinvar (benign):6 | ||||
chr17:68044066-68044373 | Common:1; Rare:83 | ||||
chr17:76557676-76557825 | Rare:51 | ||||
chr18:5238025-5238139 | Common:1; Rare:45 | ||||
chr19:27793162-27793471 | Common:4; Rare:74 | ||||
chr19:41352814-41352917 | Rare:24 |