Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66533274-66533659 | Common:2; Rare:61 | ||||
chr1:66533672-66534176 | Common:2; Rare:123 | ||||
chr1:66924773-66925031 | Common:2; Rare:117 | ||||
chr1:66925188-66925514 | Common:2; Rare:102 | ||||
chr1:66930077-66930393 | Rare:102 | ||||
chr1:67054102-67054458 | Common:6; Rare:73 | ||||
chr1:67429989-67430059 | Rare:30 | ||||
chr1:67833332-67833519 | Common:2; Rare:76 | ||||
chr1:68232451-68232643 | Rare:44 | ||||
chr1:70205491-70205778 | Rare:104 | ||||
chr1:70221278-70221649 | Rare:144 | ||||
chr1:70354664-70354862 | Rare:66 | ||||
chr1:70411069-70411285 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080971-71081388 | Rare:115 | ||||
chr1:72282697-72283303 | Common:8; Rare:192 |