Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11099580-11100057 | Common:4; Rare:181 | ||||
chr1:11262441-11262923 | Common:3; Rare:140 | ||||
chr1:11272948-11273335 | Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273398-11273519 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273598-11273736 | Rare:41 | ||||
chr1:11479109-11479230 | Common:4; Rare:53 | ||||
chr1:11654792-11654925 | Common:2; Rare:38 | ||||
chr1:11664065-11664274 | Common:1; Rare:64 | ||||
chr1:11664715-11664742 | Rare:4 | ||||
chr1:11680686-11680738 | Rare:19 | ||||
chr1:11680962-11681057 | Rare:14 | ||||
chr1:11681091-11681345 | Common:2; Rare:90 | ||||
chr1:11681470-11681547 | Common:1; Rare:13 | ||||
chr1:11691104-11691360 | Common:3; Rare:66 | ||||
chr1:11691375-11691587 | Common:2; Rare:49 |