Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:203007268-203007435 | Common:1; Rare:65 | ||||
chr1:203305307-203305530 | Common:3; Rare:58 | ||||
chr1:203626679-203626832 | Common:1; Rare:40 | ||||
chr1:204516243-204516413 | Rare:43 | ||||
chr1:206612414-206612657 | Common:5; Rare:73 | ||||
chr1:207751856-207752183 | Common:1; Rare:111 | ||||
chr1:209652421-209652609 | Common:2; Rare:42; Clinvar:1 | ||||
chr1:209675281-209675422 | Common:1; Rare:38 | ||||
chr1:209806066-209806341 | Common:5; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827869-209828064 | Common:1; Rare:53 | ||||
chr1:212035506-212035794 | Common:2; Rare:73 | ||||
chr1:212608478-212608761 | Rare:73 | ||||
chr1:212791765-212791926 | Common:3; Rare:63 | ||||
chr1:213015447-213015628 | Rare:54 | ||||
chr1:213051231-213051326 | Rare:37 |