| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399153-160399356 | Rare:56; Clinvar:3 | ||||
| chr3:160399463-160399712 | Rare:73; Clinvar:3 | ||||
| chr3:160428324-160428544 | Rare:41 | ||||
| chr3:160449516-160449645 | Rare:26 | ||||
| chr3:160449694-160450040 | Common:2; Rare:118 | ||||
| chr3:160565266-160565868 | Common:3; Rare:200 | ||||
| chr3:160755125-160755179 | Common:1; Rare:16 | ||||
| chr3:161105064-161105180 | Common:2; Rare:22 | ||||
| chr3:161105265-161105531 | Common:3; Rare:78 | ||||
| chr3:161221209-161221428 | Common:2; Rare:62 | ||||
| chr3:161371436-161371832 | Common:3; Rare:67 | ||||
| chr3:161371843-161371984 | Rare:30 | ||||
| chr3:161372004-161372141 | Rare:32 | ||||
| chr3:167734343-167734619 | Rare:76 | ||||
| chr3:167734804-167735239 | Common:4; Rare:144; Clinvar:1; Clinvar (benign):1 |