Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179877740-179877919 | Rare:38 | ||||
chr1:179882022-179882313 | Common:3; Rare:67 | ||||
chr1:179882488-179882924 | Rare:217; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179954700-179954834 | Rare:28 | ||||
chr1:181088494-181088711 | Rare:71 | ||||
chr1:182789659-182789778 | Common:2; Rare:38 | ||||
chr1:183023092-183023279 | Common:4; Rare:46 | ||||
chr1:183635666-183636109 | Common:5; Rare:126 | ||||
chr1:184386886-184387213 | Common:1; Rare:81 | ||||
chr1:184974300-184974694 | Rare:107 | ||||
chr1:185156701-185156765 | Common:1; Rare:37 | ||||
chr1:185156922-185157172 | Rare:60 | ||||
chr1:185317196-185317453 | Common:1; Rare:78 | ||||
chr1:186375087-186375471 | Rare:110 | ||||
chr1:186375669-186375892 | Common:1; Rare:58 |