| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:31393742-31393918 | Common:2; Rare:28 | ||||
| chr2:31646750-31647040 | Rare:45 | ||||
| chr2:31822574-31822750 | Rare:33 | ||||
| chr2:31823823-31823959 | Rare:43 | ||||
| chr2:31837233-31837524 | Common:3; Rare:70 | ||||
| chr2:31839316-31839416 | Common:2; Rare:12 | ||||
| chr2:31876282-31876582 | Common:1; Rare:56 | ||||
| chr2:31876646-31876905 | Rare:37 | ||||
| chr2:31884967-31885014 | Rare:6 | ||||
| chr2:31938357-31938650 | Common:2; Rare:67 | ||||
| chr2:31939858-31939894 | Rare:7 | ||||
| chr2:31941115-31941351 | Common:1; Rare:36 | ||||
| chr2:32067008-32067051 | Rare:5 | ||||
| chr2:32136563-32136940 | Rare:62; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:32229759-32229857 | Rare:12 |