Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67660227-67660375 | Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr16:68023209-68023296 | Common:1; Rare:22 | ||||
chr16:68245187-68245399 | Common:1; Rare:65 | ||||
chr16:68310927-68311062 | Common:1; Rare:65 | ||||
chr16:69132556-69132671 | Rare:46 | ||||
chr16:69339548-69339821 | Common:1; Rare:110; Clinvar (benign):1 | ||||
chr16:69424489-69424673 | Rare:50 | ||||
chr16:69726548-69726826 | Common:3; Rare:64 | ||||
chr16:69762287-69762367 | Rare:18 | ||||
chr16:70114125-70114376 | Common:3; Rare:91 | ||||
chr16:70289419-70289762 | Common:2; Rare:136; Clinvar:1; Clinvar (benign):2 | ||||
chr16:70299093-70299224 | Common:1; Rare:26 | ||||
chr16:70346759-70346969 | Common:2; Rare:103 | ||||
chr16:70523528-70523840 | Common:3; Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr16:71845905-71846023 | Common:1; Rare:37 |