| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2999607-2999917 | Common:10; Rare:69 | ||||
| chr6:3118594-3118763 | Common:2; Rare:60 | ||||
| chr6:3157470-3157688 | Common:6; Rare:79 | ||||
| chr6:3258825-3259020 | Rare:72 | ||||
| chr6:4021218-4021419 | Rare:93 | ||||
| chr6:5260681-5261017 | Common:3; Rare:114; Clinvar (benign):4 | ||||
| chr6:5261280-5261553 | Common:9; Rare:64 | ||||
| chr6:7107477-7107793 | Rare:105 | ||||
| chr6:7313105-7313383 | Common:4; Rare:103 | ||||
| chr6:7347490-7347645 | Common:7; Rare:30 | ||||
| chr6:7389740-7389820 | Rare:24 | ||||
| chr6:8435496-8435659 | Common:3; Rare:61 | ||||
| chr6:10585514-10585774 | Common:3; Rare:64 | ||||
| chr6:10694630-10694993 | Common:4; Rare:92 | ||||
| chr6:10722796-10723221 | Common:6; Rare:144 |