| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918783-48918895 | Common:2; Rare:65 | ||||
| chr3:49007180-49007446 | Common:2; Rare:108 | ||||
| chr3:49021503-49021673 | Rare:47; Clinvar:1 | ||||
| chr3:49021902-49022195 | Rare:89; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr3:49029357-49029573 | Common:2; Rare:159 | ||||
| chr3:49093451-49093634 | Rare:65 | ||||
| chr3:49104615-49104848 | Common:1; Rare:99; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120764-49120850 | Rare:23 | ||||
| chr3:49120868-49121005 | Rare:37 | ||||
| chr3:49132976-49133167 | Rare:40; Clinvar:2 | ||||
| chr3:49166286-49166422 | Common:1; Rare:36 | ||||
| chr3:49171518-49171636 | Common:2; Rare:29 | ||||
| chr3:49340010-49340109 | Common:2; Rare:49 | ||||
| chr3:49358244-49358458 | Common:3; Rare:114 | ||||
| chr3:49411862-49412213 | Common:1; Rare:120 |