| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47475809-47476065 | Common:3; Rare:105 | ||||
| chr3:48301320-48301477 | Common:1; Rare:49 | ||||
| chr3:48301576-48301855 | Common:7; Rare:66 | ||||
| chr3:48440035-48440271 | Common:1; Rare:71 | ||||
| chr3:48847729-48847970 | Common:1; Rare:70 | ||||
| chr3:48918768-48918920 | Common:2; Rare:88 | ||||
| chr3:48989763-48989946 | Rare:43 | ||||
| chr3:48990141-48990254 | Rare:27 | ||||
| chr3:49022011-49022174 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029385-49029764 | Common:2; Rare:188 | ||||
| chr3:49120769-49121111 | Rare:95 | ||||
| chr3:49132904-49133104 | Rare:35; Clinvar:1 | ||||
| chr3:49411902-49412429 | Common:2; Rare:195 | ||||
| chr3:49674228-49674398 | Common:1; Rare:64 | ||||
| chr3:49689471-49689597 | Rare:38 |