Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40531497-40531852 | Common:2; Rare:77 | ||||
chr1:40691504-40691864 | Common:2; Rare:160 | ||||
chr1:40692027-40692157 | Rare:51 | ||||
chr1:40709154-40709414 | Rare:59 | ||||
chr1:40979621-40979758 | Common:1; Rare:48 | ||||
chr1:41162296-41162558 | Common:1; Rare:46 | ||||
chr1:41242075-41242319 | Rare:71 | ||||
chr1:42335157-42335423 | Common:5; Rare:128 | ||||
chr1:42456010-42456110 | Rare:33 | ||||
chr1:42456211-42456575 | Common:1; Rare:105 | ||||
chr1:42658263-42658501 | Common:2; Rare:72 | ||||
chr1:42682125-42682432 | Common:2; Rare:83 | ||||
chr1:42682607-42682731 | Common:1; Rare:51 | ||||
chr1:42766577-42766729 | Rare:38; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42766984-42767317 | Common:5; Rare:113; Clinvar (benign):1 |