| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31815327-31815572 | Common:1; Rare:85 | ||||
| chr6:31834579-31834872 | Common:2; Rare:57 | ||||
| chr6:31835052-31835117 | Rare:27 | ||||
| chr6:31897649-31897782 | Rare:27 | ||||
| chr6:31945824-31946257 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31958881-31959204 | Rare:108; Clinvar:8 | ||||
| chr6:32117672-32117977 | Common:2; Rare:71 | ||||
| chr6:32130164-32130433 | Common:3; Rare:45 | ||||
| chr6:32153268-32153606 | Rare:56 | ||||
| chr6:32153757-32154225 | Common:4; Rare:79 | ||||
| chr6:32154364-32154492 | Rare:15 | ||||
| chr6:32176041-32176258 | Common:1; Rare:45 | ||||
| chr6:32178085-32178651 | Common:3; Rare:117 | ||||
| chr6:32190148-32190344 | Rare:36 | ||||
| chr6:32192509-32192686 | Rare:36 |