| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43059828-43059893 | Rare:21 | ||||
| chr6:43076125-43076477 | Rare:115 | ||||
| chr6:43182011-43182233 | Common:1; Rare:64 | ||||
| chr6:43243345-43243476 | Common:1; Rare:26 | ||||
| chr6:43244092-43244247 | Common:3; Rare:27 | ||||
| chr6:43427465-43427669 | Rare:56 | ||||
| chr6:43427780-43427893 | Rare:23 | ||||
| chr6:43477319-43477597 | Common:2; Rare:57 | ||||
| chr6:43510298-43510424 | Common:2; Rare:40 | ||||
| chr6:43516850-43517123 | Common:5; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575903-43576190 | Common:1; Rare:113; Clinvar:4 | ||||
| chr6:43628866-43628920 | Rare:21 | ||||
| chr6:43629158-43629580 | Common:2; Rare:116 | ||||
| chr6:43635740-43635902 | Common:1; Rare:44 | ||||
| chr6:43687757-43687894 | Common:1; Rare:53 |