| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44761590-44761833 | Common:3; Rare:87 | ||||
| chr3:44861766-44861925 | Common:2; Rare:72 | ||||
| chr3:44976120-44976278 | Common:2; Rare:65 | ||||
| chr3:45995802-45995882 | Rare:22; Clinvar:1 | ||||
| chr3:47380806-47381072 | Rare:84 | ||||
| chr3:47475812-47476078 | Common:3; Rare:107 | ||||
| chr3:48088767-48089060 | Rare:94 | ||||
| chr3:48440050-48440341 | Common:1; Rare:118 | ||||
| chr3:48556778-48557173 | Common:1; Rare:91 | ||||
| chr3:48847676-48847973 | Common:1; Rare:84 | ||||
| chr3:48918783-48918922 | Common:2; Rare:82 | ||||
| chr3:49007311-49007429 | Common:1; Rare:55 | ||||
| chr3:49029382-49029693 | Common:2; Rare:175 | ||||
| chr3:49104683-49104898 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:49166289-49166426 | Common:1; Rare:36 |