| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2971243-2971728 | Common:6; Rare:124 | ||||
| chr6:2971740-2972089 | Common:2; Rare:70 | ||||
| chr6:2988350-2988732 | Common:3; Rare:56 | ||||
| chr6:3063777-3063971 | Common:1; Rare:74 | ||||
| chr6:3068285-3068622 | Common:1; Rare:114 | ||||
| chr6:3068909-3069080 | Common:1; Rare:74 | ||||
| chr6:3118346-3118770 | Common:6; Rare:142 | ||||
| chr6:3157091-3157151 | Common:1; Rare:10 | ||||
| chr6:3157412-3157753 | Common:8; Rare:106; Clinvar (benign):1 | ||||
| chr6:3231714-3231797 | Rare:11 | ||||
| chr6:3751277-3751366 | Common:1; Rare:27 | ||||
| chr6:4021186-4021467 | Rare:120 | ||||
| chr6:5003603-5003843 | Common:6; Rare:76 | ||||
| chr6:5132817-5132985 | Common:1; Rare:38 | ||||
| chr6:5260671-5261648 | Common:21; Rare:307; Clinvar (benign):4 |