| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44976102-44976299 | Common:3; Rare:81 | ||||
| chr3:45026218-45026394 | Common:1; Rare:52 | ||||
| chr3:45689150-45689455 | Common:2; Rare:103 | ||||
| chr3:46979568-46979827 | Common:1; Rare:57; Clinvar:1 | ||||
| chr3:47164075-47164290 | Rare:55 | ||||
| chr3:47380812-47381074 | Rare:82 | ||||
| chr3:47475809-47476061 | Common:3; Rare:105 | ||||
| chr3:48301353-48301462 | Common:1; Rare:31 | ||||
| chr3:48440062-48440287 | Common:1; Rare:75 | ||||
| chr3:48847781-48847981 | Rare:71 | ||||
| chr3:49007069-49007424 | Common:2; Rare:132 | ||||
| chr3:49007536-49007610 | Rare:20 | ||||
| chr3:49021503-49021791 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49022011-49022154 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49120798-49121116 | Rare:87 |