| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73926695-73926927 | Common:2; Rare:110; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:74147862-74148091 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178796-74179012 | Common:2; Rare:60 | ||||
| chr2:74198434-74198671 | Rare:102 | ||||
| chr2:74458157-74458509 | Common:1; Rare:111 | ||||
| chr2:74465350-74465455 | Common:1; Rare:29; Clinvar:1 | ||||
| chr2:74482975-74483112 | Rare:55 | ||||
| chr2:74503024-74503161 | Rare:31 | ||||
| chr2:74503295-74503490 | Rare:52 | ||||
| chr2:74507648-74507789 | Rare:33 | ||||
| chr2:74529653-74530036 | Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74554097-74554391 | Common:1; Rare:68 | ||||
| chr2:74554406-74554757 | Common:2; Rare:104 | ||||
| chr2:74555685-74555798 | Common:1; Rare:31 | ||||
| chr2:74833848-74834166 | Rare:94 |