Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241640189-241640606 | Common:7; Rare:149 | ||||
chr1:241749184-241749415 | Common:2; Rare:29 | ||||
chr1:241847723-241848275 | Common:6; Rare:140 | ||||
chr1:241849200-241849359 | Common:4; Rare:29 | ||||
chr1:242524098-242524179 | Rare:21 | ||||
chr1:242524290-242524459 | Common:1; Rare:48 | ||||
chr1:242524601-242524973 | Common:1; Rare:114 | ||||
chr1:243253427-243253656 | Common:2; Rare:31 | ||||
chr1:243254337-243254759 | Common:4; Rare:98 | ||||
chr1:243254845-243255591 | Common:2; Rare:182 | ||||
chr1:243255691-243256169 | Common:1; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
chr1:243256191-243256404 | Common:1; Rare:65 | ||||
chr1:243849489-243849728 | Rare:70 | ||||
chr1:243851533-243851624 | Rare:18 | ||||
chr1:244048145-244048572 | Rare:139 |