Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42668134-42668161 | Rare:5 | ||||
chr1:42696516-42696647 | Common:1; Rare:32 | ||||
chr1:42698368-42698519 | Rare:21 | ||||
chr1:42929809-42929928 | Common:1; Rare:22; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:44644771-44645068 | Common:2; Rare:65 | ||||
chr1:44778660-44778941 | Common:1; Rare:67 | ||||
chr1:48245202-48245324 | Common:1; Rare:25 | ||||
chr1:58781580-58782438 | Common:1; Rare:210; Clinvar:1 | ||||
chr1:58782441-58782992 | Common:1; Rare:185 | ||||
chr1:58783018-58783306 | Common:2; Rare:84 | ||||
chr1:58783308-58783600 | Common:1; Rare:75 | ||||
chr1:58783707-58783821 | Rare:27 | ||||
chr1:58784921-58785218 | Common:2; Rare:64 | ||||
chr1:58816309-58816530 | Common:1; Rare:54 | ||||
chr1:62800935-62801008 | Common:1; Rare:6 |