| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178822-74179004 | Common:2; Rare:48 | ||||
| chr2:74374615-74374763 | Rare:34 | ||||
| chr2:74391795-74392081 | Common:2; Rare:146 | ||||
| chr2:74421601-74421771 | Rare:56 | ||||
| chr2:74458109-74458504 | Common:1; Rare:119 | ||||
| chr2:74482928-74483098 | Common:1; Rare:58 | ||||
| chr2:74507669-74507897 | Common:1; Rare:62 | ||||
| chr2:74529668-74529997 | Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958876-74959027 | Rare:58 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84904957-84905718 | Common:4; Rare:193 | ||||
| chr2:85327919-85328080 | Common:2; Rare:74 | ||||
| chr2:85354526-85354792 | Common:1; Rare:85 | ||||
| chr2:85538893-85539171 | Common:1; Rare:93 | ||||
| chr2:85561431-85561657 | Common:1; Rare:80; Clinvar:4 |