| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2971729-2971864 | Rare:29 | ||||
| chr6:2988341-2988673 | Common:2; Rare:43 | ||||
| chr6:2999585-3000081 | Common:12; Rare:112 | ||||
| chr6:3063788-3063968 | Common:1; Rare:70 | ||||
| chr6:3068411-3068570 | Common:1; Rare:53 | ||||
| chr6:3118355-3118737 | Common:5; Rare:124 | ||||
| chr6:3157447-3157642 | Common:6; Rare:74; Clinvar (benign):1 | ||||
| chr6:3231730-3231817 | Rare:15 | ||||
| chr6:4021193-4021465 | Rare:116 | ||||
| chr6:4135210-4135249 | Rare:11 | ||||
| chr6:5003603-5003832 | Common:6; Rare:71 | ||||
| chr6:5003998-5004126 | Common:2; Rare:57 | ||||
| chr6:5260661-5261026 | Common:3; Rare:126; Clinvar (benign):4 | ||||
| chr6:5261275-5261559 | Common:9; Rare:71 | ||||
| chr6:6006858-6007102 | Common:3; Rare:55 |