Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70087777-70087866 | Rare:21 | ||||
chr2:70258033-70258203 | Common:2; Rare:62 | ||||
chr2:70293659-70293811 | Common:2; Rare:52 | ||||
chr2:71068539-71068678 | Rare:61 | ||||
chr2:71130194-71130687 | Common:6; Rare:146; Clinvar:1; Clinvar (benign):2 | ||||
chr2:72147741-72147942 | Rare:62 | ||||
chr2:73070656-73070726 | Rare:17 | ||||
chr2:73071701-73071861 | Common:2; Rare:60 | ||||
chr2:73214120-73214311 | Common:1; Rare:65 | ||||
chr2:73828804-73829029 | Common:1; Rare:53 | ||||
chr2:74147870-74148140 | Common:1; Rare:66; Clinvar:2 | ||||
chr2:74421639-74421768 | Rare:42 | ||||
chr2:74458126-74458494 | Common:1; Rare:111 | ||||
chr2:74482995-74483099 | Rare:41 | ||||
chr2:74507321-74507504 | Rare:56 |