| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31977833-31977939 | Rare:17 | ||||
| chr3:31979807-31980145 | Common:1; Rare:70 | ||||
| chr3:32476475-32476724 | Common:1; Rare:41 | ||||
| chr3:32485020-32485090 | Common:3; Rare:8 | ||||
| chr3:32601334-32601504 | Rare:31 | ||||
| chr3:33051792-33051921 | Rare:33; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:33339475-33339572 | Common:1; Rare:17 | ||||
| chr3:33395556-33395780 | Common:2; Rare:52 | ||||
| chr3:33593637-33593706 | Rare:8 | ||||
| chr3:33793697-33793783 | Rare:10 | ||||
| chr3:33795195-33795523 | Rare:53 | ||||
| chr3:33816579-33816711 | Rare:22 | ||||
| chr3:33853852-33853905 | Common:1; Rare:11 | ||||
| chr3:33866318-33866395 | Common:2; Rare:17 | ||||
| chr3:35877059-35877089 | Rare:8 |