| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32637270-32637445 | Common:17; Rare:15 | ||||
| chr6:32843992-32844130 | Rare:31; Clinvar:1 | ||||
| chr6:32844334-32844452 | Rare:31 | ||||
| chr6:32844585-32844848 | Common:1; Rare:55 | ||||
| chr6:32853660-32853764 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853979-32854250 | Common:2; Rare:64 | ||||
| chr6:32968461-32968609 | Common:2; Rare:41 | ||||
| chr6:32968812-32968923 | Common:4; Rare:39 | ||||
| chr6:32970183-32970256 | Common:1; Rare:18 | ||||
| chr6:32970735-32970964 | Common:1; Rare:62 | ||||
| chr6:32977475-32977841 | Common:2; Rare:125; Clinvar (benign):1 | ||||
| chr6:33075713-33076053 | Common:6; Rare:46 | ||||
| chr6:33200356-33200449 | Rare:24 | ||||
| chr6:33200656-33200966 | Common:3; Rare:92 | ||||
| chr6:33204990-33205253 | Common:3; Rare:78 |