Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775462-44775599 | Rare:53 | ||||
chr1:44775835-44776140 | Common:2; Rare:111 | ||||
chr1:45500056-45500353 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45550762-45551076 | Common:3; Rare:78 | ||||
chr1:45583927-45584050 | Rare:45 | ||||
chr1:45687050-45687312 | Common:1; Rare:73 | ||||
chr1:45688078-45688233 | Common:1; Rare:48 | ||||
chr1:46198409-46198499 | Common:1; Rare:34; Clinvar:1 | ||||
chr1:46303174-46303763 | Common:3; Rare:181 | ||||
chr1:46340547-46340821 | Common:6; Rare:70 | ||||
chr1:47333794-47333979 | Common:2; Rare:66 | ||||
chr1:48776730-48776765 | Rare:7 | ||||
chr1:52055158-52055256 | Common:1; Rare:23 | ||||
chr1:52056118-52056338 | Common:1; Rare:64 | ||||
chr1:52404416-52404626 | Common:1; Rare:62 |