| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184154850-184155146 | Rare:100 | ||||
| chr3:184155107-184155587 | Common:2; Rare:302 | ||||
| chr3:184174750-184174982 | Common:2; Rare:64 | ||||
| chr3:184181698-184181991 | Rare:62 | ||||
| chr3:184185788-184186256 | Common:13; Rare:420 | ||||
| chr3:184248817-184249058 | Common:4; Rare:297; Clinvar:15; Clinvar (benign):7 | ||||
| chr3:184249454-184249794 | Common:3; Rare:298 | ||||
| chr3:184261454-184261918 | Common:2; Rare:254 | ||||
| chr3:184298821-184299347 | Common:16; Rare:386 | ||||
| chr3:184299659-184300403 | Common:8; Rare:276 | ||||
| chr3:184306922-184307322 | Common:2; Rare:144 | ||||
| chr3:184314369-184314821 | Common:12; Rare:307 | ||||
| chr3:184314928-184315255 | Rare:133 | ||||
| chr3:184315260-184315516 | Common:1; Rare:218 | ||||
| chr3:184315490-184315909 | Common:5; Rare:189 |