Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45205600-45206300 | Common:2; Rare:318 | ||||
chr1:45206324-45206723 | Common:3; Rare:318 | ||||
chr1:45326576-45326897 | Rare:68 | ||||
chr1:45339490-45339787 | Common:1; Rare:116 | ||||
chr1:45339702-45339818 | Rare:27 | ||||
chr1:45339873-45340487 | Common:8; Rare:551; Clinvar:41; Clinvar (benign):24; Clinvar (pathogenic):3 | ||||
chr1:45490977-45491448 | Common:7; Rare:204 | ||||
chr1:45499932-45500396 | Common:6; Rare:288; Clinvar:13; Clinvar (pathogenic):9 | ||||
chr1:45521500-45522152 | Common:3; Rare:433 | ||||
chr1:45550690-45551130 | Common:9; Rare:290 | ||||
chr1:45583192-45583610 | Common:7; Rare:150 | ||||
chr1:45583785-45584086 | Common:1; Rare:198 | ||||
chr1:45686412-45686883 | Rare:304 | ||||
chr1:45686962-45687452 | Common:6; Rare:316 | ||||
chr1:45688050-45688246 | Common:2; Rare:109 |