| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3118589-3118755 | Common:2; Rare:57 | ||||
| chr6:3157482-3157669 | Common:6; Rare:72 | ||||
| chr6:3849056-3849378 | Common:4; Rare:86 | ||||
| chr6:4021212-4021423 | Rare:97 | ||||
| chr6:5003662-5003834 | Common:5; Rare:52 | ||||
| chr6:5260696-5261032 | Common:5; Rare:112; Clinvar (benign):4 | ||||
| chr6:7108577-7108674 | Rare:32 | ||||
| chr6:7313049-7313404 | Common:5; Rare:131 | ||||
| chr6:7389777-7389875 | Common:1; Rare:27 | ||||
| chr6:7541334-7542096 | Common:6; Rare:252; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr6:8435467-8435659 | Common:4; Rare:73 | ||||
| chr6:10694595-10694978 | Common:5; Rare:102 | ||||
| chr6:10722860-10723220 | Common:6; Rare:124 | ||||
| chr6:10747569-10747876 | Common:4; Rare:117 | ||||
| chr6:11232640-11232810 | Rare:35 |