| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49120860-49121187 | Rare:86; Clinvar:1 | ||||
| chr3:49132912-49133141 | Rare:43; Clinvar:2 | ||||
| chr3:49166294-49166466 | Common:1; Rare:40 | ||||
| chr3:49339986-49340122 | Common:2; Rare:67 | ||||
| chr3:49411820-49412423 | Common:2; Rare:208 | ||||
| chr3:49469986-49470298 | Common:1; Rare:91 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49689471-49689613 | Rare:43 | ||||
| chr3:49723937-49724181 | Common:7; Rare:80 | ||||
| chr3:50267405-50267658 | Common:2; Rare:83 | ||||
| chr3:50299320-50299683 | Common:1; Rare:90 | ||||
| chr3:50328173-50328346 | Rare:51 | ||||
| chr3:50350711-50350894 | Common:1; Rare:28 | ||||
| chr3:50567608-50567895 | Common:1; Rare:87 | ||||
| chr3:50569406-50569499 | Rare:20 |