Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167093889-167094182 | Common:2; Rare:62 | ||||
chr1:167630114-167630352 | Common:4; Rare:43 | ||||
chr1:167935756-167936329 | Common:3; Rare:166 | ||||
chr1:167936549-167936727 | Rare:58 | ||||
chr1:167936853-167936974 | Rare:49 | ||||
chr1:168178729-168179123 | Common:4; Rare:121 | ||||
chr1:168225913-168226056 | Common:1; Rare:48 | ||||
chr1:169107628-169107966 | Common:3; Rare:77 | ||||
chr1:169367761-169368254 | Common:3; Rare:93 | ||||
chr1:169485716-169485790 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):4 | ||||
chr1:169485929-169486273 | Common:1; Rare:83; Clinvar:1 | ||||
chr1:169711601-169711762 | Rare:40 | ||||
chr1:169794685-169794747 | Rare:12 | ||||
chr1:169794868-169795094 | Common:3; Rare:58 | ||||
chr1:170074459-170074762 | Common:2; Rare:93 |