Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66604033-66604359 | Common:7; Rare:78 | ||||
chr16:66918819-66919049 | Common:1; Rare:48 | ||||
chr16:66934272-66934515 | Common:1; Rare:90 | ||||
chr16:67028985-67029124 | Rare:48 | ||||
chr16:67109804-67109994 | Rare:61 | ||||
chr16:67183951-67184036 | Common:1; Rare:25 | ||||
chr16:67227004-67227167 | Rare:65 | ||||
chr16:67247474-67247767 | Common:1; Rare:82 | ||||
chr16:67326731-67326986 | Common:1; Rare:84 | ||||
chr16:67481088-67481399 | Common:1; Rare:118 | ||||
chr16:67518074-67518532 | Common:1; Rare:91 | ||||
chr16:67528424-67528591 | Rare:27 | ||||
chr16:67528698-67528884 | Rare:53 | ||||
chr16:67660222-67660379 | Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67660745-67661030 | Common:2; Rare:99 |