| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:232950431-232950658 | Common:4; Rare:86 | ||||
| chr1:234373346-234373591 | Common:1; Rare:121; Clinvar (benign):4 | ||||
| chr1:234373650-234373789 | Rare:48; Clinvar (benign):3 | ||||
| chr1:235128767-235129060 | Common:1; Rare:119 | ||||
| chr1:235328116-235328430 | Common:2; Rare:90 | ||||
| chr1:235328463-235328614 | Common:2; Rare:53 | ||||
| chr1:235866898-235867137 | Common:2; Rare:69 | ||||
| chr1:236281943-236282116 | Common:3; Rare:50 | ||||
| chr1:236523845-236524024 | Common:2; Rare:48 | ||||
| chr1:236604462-236604626 | Common:4; Rare:51 | ||||
| chr1:236795076-236795457 | Common:6; Rare:158; Clinvar:4 | ||||
| chr1:241519667-241519924 | Common:2; Rare:89; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr1:241848078-241848255 | Common:2; Rare:37 | ||||
| chr1:243255142-243255415 | Common:1; Rare:59 | ||||
| chr1:243255776-243256088 | Rare:84; Clinvar:4 |