Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69762268-69762381 | Common:1; Rare:28 | ||||
chr16:70289434-70289802 | Common:3; Rare:147; Clinvar:1 | ||||
chr16:70299093-70299230 | Common:1; Rare:29 | ||||
chr16:70346759-70346957 | Common:1; Rare:96 | ||||
chr16:70454509-70454605 | Common:1; Rare:31 | ||||
chr16:70523517-70523881 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:71484024-71484316 | Common:2; Rare:74 | ||||
chr16:71809042-71809316 | Common:3; Rare:90 | ||||
chr16:71845912-71846013 | Common:1; Rare:32 | ||||
chr16:71883468-71883642 | Rare:49 | ||||
chr16:71895234-71895545 | Common:2; Rare:118 | ||||
chr16:72008490-72008788 | Common:6; Rare:116; Clinvar (benign):2 | ||||
chr16:72093548-72093937 | Rare:100 | ||||
chr16:74607095-74607213 | Rare:62 | ||||
chr16:74666856-74667098 | Common:1; Rare:78 |