| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31681403-31681650 | Rare:46 | ||||
| chr6:31703268-31703415 | Rare:49 | ||||
| chr6:31728690-31728953 | Rare:68 | ||||
| chr6:31729764-31730094 | Common:2; Rare:57 | ||||
| chr6:31730136-31730729 | Common:3; Rare:122 | ||||
| chr6:31736261-31736610 | Common:2; Rare:86 | ||||
| chr6:31753343-31753630 | Rare:92 | ||||
| chr6:31759879-31760169 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr6:31777264-31777532 | Common:2; Rare:50 | ||||
| chr6:31806781-31807038 | Common:1; Rare:102 | ||||
| chr6:31836426-31836615 | Common:1; Rare:42 | ||||
| chr6:31837019-31837075 | Rare:17 | ||||
| chr6:31837242-31837464 | Common:2; Rare:76 | ||||
| chr6:31897679-31897796 | Rare:23 | ||||
| chr6:31958698-31959206 | Common:2; Rare:151; Clinvar:8; Clinvar (benign):1 |