| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43042899-43043140 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:43223895-43224022 | Common:1; Rare:18 | ||||
| chr6:43368750-43368807 | Rare:18 | ||||
| chr6:43674848-43675008 | Rare:30 | ||||
| chr6:43678130-43678230 | Rare:23 | ||||
| chr6:43852276-43852387 | Common:1; Rare:20 | ||||
| chr6:43998791-43998873 | Common:1; Rare:14 | ||||
| chr6:44154416-44154731 | Common:2; Rare:79 | ||||
| chr6:44249412-44249856 | Common:1; Rare:123 | ||||
| chr6:44249918-44250483 | Common:5; Rare:198 | ||||
| chr6:44251278-44251608 | Common:2; Rare:94 | ||||
| chr6:44251633-44252213 | Common:3; Rare:205 | ||||
| chr6:44551507-44551625 | Rare:23 | ||||
| chr6:44727733-44727955 | Common:2; Rare:60 | ||||
| chr6:45575089-45575215 | Rare:30 |