Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66552492-66552682 | Rare:80 | ||||
chr16:66934345-66934515 | Common:1; Rare:64 | ||||
chr16:67000512-67000580 | Rare:15 | ||||
chr16:67159884-67160016 | Rare:21 | ||||
chr16:67170434-67170550 | Common:1; Rare:17 | ||||
chr16:67183923-67183993 | Common:1; Rare:24 | ||||
chr16:67227004-67227167 | Rare:65 | ||||
chr16:67247451-67247489 | Rare:11 | ||||
chr16:67393469-67393680 | Common:1; Rare:48 | ||||
chr16:67481093-67481399 | Common:1; Rare:116 | ||||
chr16:67528654-67528883 | Rare:58 | ||||
chr16:67660221-67660364 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67666744-67666870 | Rare:25 | ||||
chr16:67719248-67719473 | Common:1; Rare:62 | ||||
chr16:67966779-67967039 | Rare:51 |