| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736815-197737138 | Common:3; Rare:100 | ||||
| chr3:197749777-197749962 | Common:1; Rare:71 | ||||
| chr3:197949882-197950266 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr3:197959982-197960245 | Common:1; Rare:92 | ||||
| chr4:499141-499324 | Common:2; Rare:67 | ||||
| chr4:673839-674007 | Rare:68 | ||||
| chr4:674211-674614 | Common:4; Rare:185 | ||||
| chr4:705589-705922 | Common:1; Rare:113 | ||||
| chr4:932131-932487 | Common:2; Rare:138 | ||||
| chr4:986918-987044 | Common:1; Rare:33; Clinvar:1 | ||||
| chr4:993402-993537 | Common:3; Rare:16 | ||||
| chr4:1113524-1113630 | Common:2; Rare:38 | ||||
| chr4:1249090-1249200 | Rare:22 | ||||
| chr4:1289656-1289973 | Common:1; Rare:114 | ||||
| chr4:1712310-1712486 | Common:2; Rare:54 |