Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209675225-209675431 | Common:2; Rare:52 | ||||
chr1:209937977-209938267 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
chr1:211259077-211259399 | Common:1; Rare:104 | ||||
chr1:211259735-211259970 | Rare:66 | ||||
chr1:212035510-212035801 | Common:2; Rare:77 | ||||
chr1:212791759-212791926 | Common:3; Rare:66 | ||||
chr1:216723420-216723522 | Rare:25 | ||||
chr1:217089606-217089743 | Rare:34 | ||||
chr1:217631020-217631379 | Common:2; Rare:100 | ||||
chr1:218285212-218285385 | Common:2; Rare:80 | ||||
chr1:218345760-218346128 | Common:5; Rare:107; Clinvar:9; Clinvar (benign):4 | ||||
chr1:219173786-219173916 | Common:1; Rare:76 | ||||
chr1:220272376-220272576 | Rare:55; Clinvar:5 | ||||
chr1:222589871-222589970 | Common:2; Rare:25 | ||||
chr1:222644094-222644412 | Common:3; Rare:94 |