| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184017864-184018078 | Common:1; Rare:65 | ||||
| chr3:184135221-184135490 | Common:2; Rare:92; Clinvar:6 | ||||
| chr3:184185905-184186210 | Common:4; Rare:112 | ||||
| chr3:184248914-184249021 | Rare:48; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249527-184249678 | Rare:40 | ||||
| chr3:184298935-184299269 | Common:3; Rare:101 | ||||
| chr3:184337454-184337639 | Rare:36 | ||||
| chr3:184361601-184361765 | Rare:43 | ||||
| chr3:184711943-184712243 | Common:1; Rare:102 | ||||
| chr3:185152895-185153106 | Common:4; Rare:72 | ||||
| chr3:185282849-185283006 | Common:1; Rare:40 | ||||
| chr3:185498917-185499155 | Rare:87 | ||||
| chr3:185586033-185586358 | Common:1; Rare:72 | ||||
| chr3:186567281-186567439 | Common:3; Rare:44 | ||||
| chr3:186783248-186783646 | Common:1; Rare:174 |