Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61076970-61077224 | Common:3; Rare:69 | ||||
chr1:61725037-61725198 | Rare:84 | ||||
chr1:62688266-62688535 | Common:1; Rare:104 | ||||
chr1:62784041-62784180 | Rare:55 | ||||
chr1:63367508-63367675 | Rare:47; Clinvar (benign):1 | ||||
chr1:63523186-63523588 | Common:3; Rare:101 | ||||
chr1:65309220-65309582 | Common:1; Rare:94 | ||||
chr1:66533333-66533636 | Common:2; Rare:40 | ||||
chr1:66533877-66534190 | Common:2; Rare:75 | ||||
chr1:66924800-66925024 | Rare:97 | ||||
chr1:66925182-66925503 | Common:2; Rare:103 | ||||
chr1:66930042-66930377 | Rare:114 | ||||
chr1:67429993-67430221 | Rare:82 | ||||
chr1:68232515-68232676 | Rare:34 | ||||
chr1:70205522-70205775 | Rare:86 |