| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49358100-49358458 | Common:4; Rare:187 | ||||
| chr3:49411880-49412213 | Common:1; Rare:115 | ||||
| chr3:49412250-49412445 | Common:1; Rare:68 | ||||
| chr3:49429255-49429461 | Common:1; Rare:44 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49689447-49689597 | Rare:50 | ||||
| chr3:49723893-49724164 | Common:6; Rare:87 | ||||
| chr3:49803177-49803334 | Rare:56 | ||||
| chr3:49856538-49856695 | Common:2; Rare:45 | ||||
| chr3:50267411-50267658 | Common:2; Rare:81 | ||||
| chr3:50299282-50299471 | Rare:44 | ||||
| chr3:50328161-50328373 | Rare:66 | ||||
| chr3:50350711-50350905 | Common:1; Rare:31 | ||||
| chr3:50359379-50359729 | Common:3; Rare:101 | ||||
| chr3:50365139-50365372 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 |