| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122152256-122152530 | Common:2; Rare:99 | ||||
| chr4:122732425-122732776 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122922510-122922675 | Common:3; Rare:82 | ||||
| chr4:122922982-122923145 | Common:1; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123399338-123399653 | Common:1; Rare:96 | ||||
| chr4:127880764-127880929 | Rare:61 | ||||
| chr4:127965896-127966013 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr4:128060994-128061329 | Common:1; Rare:118 | ||||
| chr4:128287789-128287965 | Common:2; Rare:73 | ||||
| chr4:128288208-128288285 | Common:3; Rare:26 | ||||
| chr4:128811162-128811349 | Rare:43 | ||||
| chr4:129093458-129093761 | Common:1; Rare:89 | ||||
| chr4:133149066-133149325 | Common:2; Rare:78 | ||||
| chr4:139177134-139177456 | Rare:94 | ||||
| chr4:139280088-139280498 | Common:1; Rare:103 |