Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167935957-167936327 | Common:2; Rare:112 | ||||
chr1:167936544-167936968 | Common:1; Rare:153 | ||||
chr1:168178748-168179083 | Common:4; Rare:111 | ||||
chr1:168225886-168226056 | Common:1; Rare:58 | ||||
chr1:169367788-169368256 | Common:3; Rare:87 | ||||
chr1:169427460-169427506 | Rare:10 | ||||
chr1:169485705-169486219 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794890-169795053 | Common:3; Rare:34 | ||||
chr1:170074483-170074553 | Rare:22 | ||||
chr1:170074569-170074740 | Common:1; Rare:46 | ||||
chr1:170532040-170532201 | Rare:73; Clinvar:1 | ||||
chr1:170663042-170663197 | Rare:36 | ||||
chr1:170664056-170664389 | Common:3; Rare:98 | ||||
chr1:171485218-171485598 | Rare:112 | ||||
chr1:171652259-171652371 | Rare:36; Clinvar:3 |