| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3118597-3118743 | Common:2; Rare:49 | ||||
| chr6:3157518-3157642 | Common:6; Rare:49 | ||||
| chr6:4021246-4021423 | Rare:91 | ||||
| chr6:5003609-5003843 | Common:6; Rare:73 | ||||
| chr6:5260702-5261013 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr6:5261296-5261553 | Common:9; Rare:57 | ||||
| chr6:7313102-7313331 | Common:5; Rare:90 | ||||
| chr6:7541368-7541684 | Common:1; Rare:94; Clinvar (benign):1 | ||||
| chr6:8435343-8435654 | Common:4; Rare:108 | ||||
| chr6:10694626-10694984 | Common:4; Rare:89 | ||||
| chr6:10747582-10747876 | Common:3; Rare:111 | ||||
| chr6:13615184-13615530 | Common:2; Rare:139 | ||||
| chr6:13615547-13615624 | Rare:30 | ||||
| chr6:16761461-16761582 | Common:2; Rare:40 | ||||
| chr6:24666779-24667214 | Common:4; Rare:181 |