| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:192917830-192918008 | Common:2; Rare:80 | ||||
| chr3:193240992-193241343 | Common:4; Rare:117 | ||||
| chr3:193593075-193593404 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486979-194487166 | Common:4; Rare:86 | ||||
| chr3:194632975-194633121 | Common:1; Rare:56 | ||||
| chr3:194633726-194633732 | |||||
| chr3:195356086-195356337 | Common:1; Rare:69 | ||||
| chr3:195543127-195543440 | Common:4; Rare:103 | ||||
| chr3:195892696-195892850 | Common:3; Rare:26 | ||||
| chr3:195895893-195895979 | Common:1; Rare:30 | ||||
| chr3:196082080-196082267 | Common:3; Rare:76 | ||||
| chr3:196287642-196287831 | Common:1; Rare:59 | ||||
| chr3:196318111-196318346 | Common:1; Rare:101 | ||||
| chr3:196432385-196432578 | Common:1; Rare:83 | ||||
| chr3:196503568-196503914 | Common:5; Rare:115 |