| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46692666-46692920 | Common:1; Rare:48 | ||||
| chr3:46960366-46960592 | Common:1; Rare:37 | ||||
| chr3:46986114-46986382 | Common:1; Rare:39 | ||||
| chr3:46987369-46987664 | Common:2; Rare:51 | ||||
| chr3:46989087-46989371 | Rare:96; Clinvar:1 | ||||
| chr3:46990536-46990706 | Rare:24 | ||||
| chr3:46998731-46999115 | Common:1; Rare:135; Clinvar:4 | ||||
| chr3:46999148-46999467 | Common:2; Rare:101; Clinvar:1 | ||||
| chr3:47415642-47415742 | Rare:15 | ||||
| chr3:47418414-47418702 | Common:1; Rare:99 | ||||
| chr3:47421985-47422167 | Common:1; Rare:44 | ||||
| chr3:47424012-47424115 | Rare:21 | ||||
| chr3:47848666-47848944 | Rare:76 | ||||
| chr3:48574816-48575082 | Common:1; Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:48575460-48575750 | Rare:84; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):5 |