Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44739667-44739887 | Common:1; Rare:83 | ||||
chr1:44775408-44775607 | Common:1; Rare:76 | ||||
chr1:44775835-44776140 | Common:2; Rare:111 | ||||
chr1:44808415-44808654 | Common:1; Rare:56 | ||||
chr1:45339996-45340178 | Rare:54 | ||||
chr1:45340381-45340470 | Common:1; Rare:24; Clinvar:1 | ||||
chr1:45500046-45500353 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521820-45522089 | Common:1; Rare:101 | ||||
chr1:45550719-45551086 | Common:3; Rare:90 | ||||
chr1:45686479-45686668 | Rare:69 | ||||
chr1:45687059-45687363 | Common:1; Rare:80 | ||||
chr1:45688061-45688243 | Common:1; Rare:54 | ||||
chr1:45750607-45750793 | Rare:68 | ||||
chr1:46198358-46198485 | Common:1; Rare:50; Clinvar:1 | ||||
chr1:46303124-46303769 | Common:3; Rare:193 |