Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156054611-156055126 | Common:4; Rare:134 | ||||
chr1:156081193-156081344 | Rare:29 | ||||
chr1:156082003-156082032 | Rare:4 | ||||
chr1:156082103-156082214 | Rare:14 | ||||
chr1:156082409-156082661 | Rare:61 | ||||
chr1:156082919-156082988 | Rare:21 | ||||
chr1:156106237-156106430 | Rare:31 | ||||
chr1:156106455-156106714 | Common:1; Rare:54 | ||||
chr1:156114184-156114455 | Rare:49 | ||||
chr1:156114544-156114860 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
chr1:156134398-156135269 | Common:5; Rare:199; Clinvar:28; Clinvar (benign):19; Clinvar (pathogenic):15 | ||||
chr1:156135898-156136435 | Common:4; Rare:174; Clinvar:39; Clinvar (benign):24; Clinvar (pathogenic):15 | ||||
chr1:156193801-156194200 | Common:3; Rare:101 | ||||
chr1:156212859-156213141 | Common:1; Rare:94 | ||||
chr1:156248514-156248598 | Common:1; Rare:7 |