Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6026155-6026437 | Common:1; Rare:62 | ||||
chr1:6235926-6236189 | Common:5; Rare:110 | ||||
chr1:6385784-6385911 | Common:1; Rare:40 | ||||
chr1:7961455-7961787 | Common:4; Rare:111; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878583-8878889 | Rare:162 | ||||
chr1:9687524-9687676 | Common:1; Rare:38 | ||||
chr1:9910309-9910621 | Common:3; Rare:105 | ||||
chr1:9943294-9943488 | Common:2; Rare:45 | ||||
chr1:11099758-11099939 | Common:3; Rare:75 | ||||
chr1:11654357-11654470 | Rare:33 | ||||
chr1:11654773-11654910 | Common:2; Rare:45 | ||||
chr1:11805900-11806228 | Common:2; Rare:88; Clinvar:1 | ||||
chr1:11926404-11926602 | Common:6; Rare:57 | ||||
chr1:13749287-13749439 | Common:1; Rare:48 | ||||
chr1:19210251-19210501 | Rare:88 |