| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196639596-196639870 | Common:3; Rare:58 | ||||
| chr3:196942387-196942680 | Common:1; Rare:120 | ||||
| chr3:197736891-197737140 | Common:2; Rare:74 | ||||
| chr3:197949942-197950230 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr3:197959982-197960245 | Common:1; Rare:92 | ||||
| chr4:499141-499301 | Common:2; Rare:60 | ||||
| chr4:663503-663734 | Common:1; Rare:69 | ||||
| chr4:673873-673982 | Rare:50 | ||||
| chr4:674211-674607 | Common:4; Rare:183 | ||||
| chr4:705589-705791 | Rare:69 | ||||
| chr4:932260-932492 | Common:2; Rare:90 | ||||
| chr4:2041892-2042061 | Common:1; Rare:65 | ||||
| chr4:2468878-2469155 | Common:3; Rare:98 | ||||
| chr4:2792840-2793121 | Common:2; Rare:81 | ||||
| chr4:2793997-2794092 | Rare:15 |