Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:221742065-221742254 | Rare:41 | ||||
chr1:222589871-222590031 | Common:2; Rare:44 | ||||
chr1:222617835-222618119 | Common:3; Rare:69 | ||||
chr1:222644127-222644431 | Common:2; Rare:93 | ||||
chr1:222712444-222712866 | Common:3; Rare:150 | ||||
chr1:222713267-222713408 | Rare:43 | ||||
chr1:223712266-223712647 | Common:2; Rare:115 | ||||
chr1:223845792-223846082 | Rare:95 | ||||
chr1:224114044-224114135 | Common:1; Rare:40 | ||||
chr1:224183110-224183293 | Common:2; Rare:86 | ||||
chr1:224330121-224330456 | Common:7; Rare:108 | ||||
chr1:225427987-225428352 | Common:3; Rare:120; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777721-225777883 | Common:3; Rare:45 | ||||
chr1:225882320-225882464 | Rare:44 | ||||
chr1:225924236-225924549 | Common:9; Rare:91 |