| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147821-74148146 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74362651-74363006 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:74391773-74392142 | Common:2; Rare:175 | ||||
| chr2:74421576-74421808 | Rare:78 | ||||
| chr2:74440399-74440881 | Rare:110 | ||||
| chr2:74458131-74458528 | Common:1; Rare:119 | ||||
| chr2:74465336-74465439 | Rare:27; Clinvar:1 | ||||
| chr2:74482921-74483089 | Common:1; Rare:54 | ||||
| chr2:74514385-74514529 | Rare:29 | ||||
| chr2:74527625-74527745 | Common:1; Rare:40 | ||||
| chr2:74529639-74530045 | Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530335-74530627 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:74548844-74549116 | Rare:77 | ||||
| chr2:74553866-74554163 | Rare:61 | ||||
| chr2:74833823-74834147 | Common:1; Rare:96 |