| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235128767-235129043 | Rare:110 | ||||
| chr1:235328138-235328407 | Common:2; Rare:78 | ||||
| chr1:235328478-235328606 | Common:2; Rare:42 | ||||
| chr1:235504435-235504754 | Common:3; Rare:91 | ||||
| chr1:235866847-235867216 | Common:3; Rare:116 | ||||
| chr1:235883185-235883901 | Common:2; Rare:128 | ||||
| chr1:236281936-236282249 | Common:6; Rare:91 | ||||
| chr1:236523889-236524024 | Common:2; Rare:36 | ||||
| chr1:236524512-236524608 | Common:1; Rare:20 | ||||
| chr1:236604420-236604636 | Common:4; Rare:67 | ||||
| chr1:236795080-236795453 | Common:6; Rare:154; Clinvar:3 | ||||
| chr1:239386489-239386623 | Rare:21 | ||||
| chr1:239719668-239720140 | Common:1; Rare:92 | ||||
| chr1:241519611-241519993 | Common:3; Rare:121; Clinvar:15; Clinvar (benign):13; Clinvar (pathogenic):4 | ||||
| chr1:241848070-241848266 | Common:2; Rare:41 |