| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196287671-196287841 | Common:1; Rare:58 | ||||
| chr3:196318135-196318373 | Common:1; Rare:102 | ||||
| chr3:196432398-196432550 | Common:1; Rare:68 | ||||
| chr3:196503684-196503835 | Common:3; Rare:44 | ||||
| chr3:196712190-196712311 | Common:1; Rare:44 | ||||
| chr3:196942368-196942659 | Common:1; Rare:119 | ||||
| chr3:197736847-197737201 | Common:3; Rare:119 | ||||
| chr3:197749826-197749998 | Rare:69 | ||||
| chr3:197791223-197791274 | Rare:25 | ||||
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959979-197960245 | Common:1; Rare:92 | ||||
| chr4:53104-53365 | Rare:5 | ||||
| chr4:337632-337867 | Rare:71 | ||||
| chr4:499124-499340 | Common:3; Rare:89 | ||||
| chr4:674215-674573 | Common:3; Rare:165 |