Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674406-44674749 | Common:3; Rare:92 | ||||
chr1:44739667-44739923 | Common:1; Rare:100 | ||||
chr1:44775377-44775411 | Rare:16 | ||||
chr1:44775418-44775625 | Common:2; Rare:83 | ||||
chr1:44775835-44776140 | Common:2; Rare:111 | ||||
chr1:44986521-44986758 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr1:45011860-45012285 | Common:6; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012693-45012811 | Common:1; Rare:21 | ||||
chr1:45339962-45340047 | Rare:28 | ||||
chr1:45340114-45340206 | Rare:42; Clinvar (benign):1 | ||||
chr1:45340385-45340502 | Common:1; Rare:31; Clinvar:1 | ||||
chr1:45500044-45500385 | Common:1; Rare:94; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521800-45522083 | Common:1; Rare:108 | ||||
chr1:45550689-45551121 | Common:3; Rare:111 | ||||
chr1:45583912-45584090 | Rare:68 |