| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196503524-196504045 | Common:9; Rare:171 | ||||
| chr3:196568518-196568848 | Common:5; Rare:101 | ||||
| chr3:196639615-196639805 | Rare:45 | ||||
| chr3:196712185-196712358 | Common:3; Rare:58 | ||||
| chr3:196867748-196867946 | Rare:67 | ||||
| chr3:196942333-196942695 | Common:1; Rare:160 | ||||
| chr3:197029780-197029928 | Common:1; Rare:48 | ||||
| chr3:197555947-197556042 | Rare:21 | ||||
| chr3:197736838-197737221 | Common:3; Rare:128 | ||||
| chr3:197749826-197750006 | Rare:70 | ||||
| chr3:197913259-197913368 | Common:10; Rare:50 | ||||
| chr3:197949885-197950298 | Common:4; Rare:122; Clinvar (benign):2 | ||||
| chr3:197951030-197951232 | Rare:63; Clinvar (benign):1 | ||||
| chr3:197959960-197960259 | Common:1; Rare:104 | ||||
| chr4:337454-337876 | Common:2; Rare:122 |