Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44186682-44186998 | Common:1; Rare:108 | ||||
chr17:44221273-44221427 | Rare:46 | ||||
chr17:44324760-44324963 | Common:2; Rare:71 | ||||
chr17:44345123-44345321 | Rare:40; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503377-44503713 | Rare:132 | ||||
chr17:45060992-45061332 | Common:2; Rare:89 | ||||
chr17:45490708-45490913 | Rare:67 | ||||
chr17:45620232-45620358 | Rare:28 | ||||
chr17:46193381-46193606 | Common:3; Rare:60 | ||||
chr17:46225349-46225481 | Common:1; Rare:34 | ||||
chr17:46922855-46923187 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47189246-47189568 | Rare:82 | ||||
chr17:47821764-47821938 | Common:1; Rare:36 | ||||
chr17:47831513-47831582 | Rare:22 | ||||
chr17:47941352-47941739 | Rare:104; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |