| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188153806-188153938 | Common:1; Rare:28 | ||||
| chr3:188154048-188154214 | Rare:45 | ||||
| chr3:189171773-189172007 | Common:1; Rare:42 | ||||
| chr3:190322436-190322528 | Rare:27 | ||||
| chr3:193240977-193241329 | Common:4; Rare:120 | ||||
| chr3:193593095-193593303 | Rare:65; Clinvar:1 | ||||
| chr3:195543127-195543449 | Common:4; Rare:107 | ||||
| chr3:196318202-196318321 | Common:1; Rare:49 | ||||
| chr3:196639623-196639796 | Rare:41 | ||||
| chr3:196712213-196712344 | Common:2; Rare:43 | ||||
| chr3:196942375-196942686 | Common:1; Rare:131 | ||||
| chr3:197736841-197737148 | Common:3; Rare:101 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959985-197960259 | Common:1; Rare:95 | ||||
| chr4:53104-53361 | Rare:5 |