| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31739751-31740023 | Common:2; Rare:64 | ||||
| chr6:31777073-31777244 | Common:1; Rare:26 | ||||
| chr6:31795714-31795990 | Common:1; Rare:60 | ||||
| chr6:31806771-31807038 | Common:1; Rare:109 | ||||
| chr6:31815271-31815557 | Common:1; Rare:88 | ||||
| chr6:31815606-31815641 | Rare:9 | ||||
| chr6:31827237-31827324 | Rare:22 | ||||
| chr6:31827416-31827941 | Common:8; Rare:208 | ||||
| chr6:31834584-31834872 | Common:2; Rare:53 | ||||
| chr6:31878968-31879089 | Common:1; Rare:34 | ||||
| chr6:31897673-31897783 | Rare:21 | ||||
| chr6:31945824-31946157 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr6:31958881-31959191 | Rare:101; Clinvar:8 | ||||
| chr6:32128184-32128534 | Common:3; Rare:86 | ||||
| chr6:32151908-32152017 | Common:7; Rare:30 |