| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31547433-31547637 | Common:2; Rare:40 | ||||
| chr6:31620370-31620699 | Common:1; Rare:100 | ||||
| chr6:31652610-31652738 | Common:1; Rare:31 | ||||
| chr6:31664956-31665097 | Common:1; Rare:29 | ||||
| chr6:31665867-31666199 | Common:4; Rare:92 | ||||
| chr6:31703277-31703441 | Rare:56 | ||||
| chr6:31721743-31721777 | Rare:4 | ||||
| chr6:31736292-31736611 | Common:1; Rare:73 | ||||
| chr6:31739751-31740012 | Common:2; Rare:58 | ||||
| chr6:31806789-31806918 | Rare:47 | ||||
| chr6:31815321-31815563 | Common:1; Rare:79 | ||||
| chr6:31827460-31827941 | Common:8; Rare:198 | ||||
| chr6:31834662-31834942 | Common:4; Rare:59 | ||||
| chr6:31897670-31897796 | Rare:24 | ||||
| chr6:31945917-31946095 | Common:1; Rare:22; Clinvar (benign):1 |