| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:75641765-75641795 | Rare:2 | ||||
| chr3:75642031-75642126 | Rare:9 | ||||
| chr3:75670340-75670536 | Rare:1 | ||||
| chr3:81760979-81761035 | Rare:9 | ||||
| chr3:81761067-81761419 | Common:2; Rare:125; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:81824158-81824267 | Rare:25 | ||||
| chr3:87088411-87088735 | Common:1; Rare:62 | ||||
| chr3:87089014-87089114 | Common:1; Rare:20 | ||||
| chr3:87792674-87792715 | Rare:17 | ||||
| chr3:87793471-87793535 | Rare:10 | ||||
| chr3:87949614-87949820 | Common:1; Rare:32 | ||||
| chr3:87949971-87950072 | Common:1; Rare:19 | ||||
| chr3:87950152-87950187 | Rare:4 | ||||
| chr3:88031895-88032249 | Common:3; Rare:65 | ||||
| chr3:88151471-88151570 | Rare:13 |