Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67159899-67160023 | Rare:22 | ||||
chr16:67170464-67170550 | Common:1; Rare:12 | ||||
chr16:67198859-67199157 | Common:2; Rare:71 | ||||
chr16:67227008-67227167 | Rare:63 | ||||
chr16:67247458-67247649 | Rare:62 | ||||
chr16:67279264-67279548 | Common:1; Rare:77 | ||||
chr16:67393378-67393645 | Rare:61 | ||||
chr16:67481037-67481380 | Common:1; Rare:121 | ||||
chr16:67528703-67528861 | Rare:44 | ||||
chr16:67660222-67660387 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67660811-67661036 | Common:2; Rare:81 | ||||
chr16:67666725-67666870 | Rare:29 | ||||
chr16:67719286-67719427 | Rare:37 | ||||
chr16:67806532-67806868 | Rare:65 | ||||
chr16:67807009-67807127 | Rare:38 |