| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106972601-106972657 | Rare:8 | ||||
| chr6:108589356-108589702 | Rare:74 | ||||
| chr6:113654508-113654677 | Rare:32 | ||||
| chr6:113858754-113859075 | Rare:69 | ||||
| chr6:117999034-117999177 | Rare:41 | ||||
| chr6:117999195-117999323 | Common:3; Rare:33 | ||||
| chr6:118895097-118895253 | Rare:44 | ||||
| chr6:127290151-127290417 | Rare:85 | ||||
| chr6:129403723-129403915 | Common:6; Rare:52; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:129481036-129481438 | Common:1; Rare:100; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr6:132817023-132817107 | Rare:32 | ||||
| chr6:135183135-135183228 | Rare:18 | ||||
| chr6:135498418-135498456 | Rare:8 | ||||
| chr6:137218706-137218823 | Rare:18 | ||||
| chr6:137868151-137868236 | Rare:15 |