| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74527470-74527757 | Common:1; Rare:97 | ||||
| chr2:74529653-74530006 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74833871-74834169 | Rare:86 | ||||
| chr2:74958338-74958671 | Common:4; Rare:96 | ||||
| chr2:74958872-74959071 | Rare:72 | ||||
| chr2:75710654-75710775 | Common:2; Rare:47 | ||||
| chr2:75710864-75711238 | Common:2; Rare:101 | ||||
| chr2:84459205-84459581 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327916-85328054 | Common:1; Rare:63 | ||||
| chr2:85354491-85354790 | Common:1; Rare:100 | ||||
| chr2:85539056-85539190 | Common:2; Rare:56 | ||||
| chr2:85539753-85540006 | Rare:66 | ||||
| chr2:85561424-85561594 | Rare:63; Clinvar:4 | ||||
| chr2:85595461-85595847 | Common:3; Rare:126 | ||||
| chr2:85602636-85602897 | Rare:67 |