| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47478070-47478251 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463141-49463449 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550251-49550795 | Common:1; Rare:109 | ||||
| chr6:52362045-52362172 | Common:1; Rare:42 | ||||
| chr6:52420108-52420385 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52577019-52577307 | Common:5; Rare:104 | ||||
| chr6:52995266-52995615 | Common:4; Rare:136 | ||||
| chr6:53064774-53064984 | Rare:62 | ||||
| chr6:53065337-53065756 | Common:1; Rare:122 | ||||
| chr6:53348823-53349099 | Common:2; Rare:132 | ||||
| chr6:53544976-53545224 | Rare:89 | ||||
| chr6:53794568-53794660 | Common:1; Rare:22 | ||||
| chr6:54846646-54846775 | Common:1; Rare:30 | ||||
| chr6:56247426-56247497 | Common:1; Rare:14 | ||||
| chr6:56247504-56247667 | Common:2; Rare:29 |