Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75979103-75979274 | Rare:48; Clinvar:4 | ||||
chr17:76353621-76353865 | Common:2; Rare:87 | ||||
chr17:76725782-76726051 | Rare:74 | ||||
chr17:76726491-76726874 | Common:5; Rare:137 | ||||
chr17:76737325-76737525 | Common:2; Rare:75 | ||||
chr17:78187042-78187371 | Common:3; Rare:105 | ||||
chr17:78680998-78681086 | Rare:22 | ||||
chr17:80415076-80415189 | Common:1; Rare:75 | ||||
chr17:80991736-80991909 | Common:2; Rare:64 | ||||
chr17:81666565-81666763 | Common:1; Rare:86 | ||||
chr17:81683693-81684057 | Common:4; Rare:183 | ||||
chr17:81703286-81703467 | Common:2; Rare:48; Clinvar (benign):1 | ||||
chr17:81833251-81833378 | Rare:55 | ||||
chr17:81860478-81860743 | Common:2; Rare:111 | ||||
chr17:81871303-81871445 | Rare:47 |