| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31736468-31736595 | Common:1; Rare:29 | ||||
| chr6:31739661-31740104 | Common:3; Rare:112 | ||||
| chr6:31760487-31760716 | Common:1; Rare:43 | ||||
| chr6:31761535-31761858 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr6:31792757-31793039 | Common:1; Rare:87 | ||||
| chr6:31795639-31795999 | Common:1; Rare:78 | ||||
| chr6:31806688-31807003 | Rare:130 | ||||
| chr6:31814947-31815179 | Common:2; Rare:50 | ||||
| chr6:31815310-31815566 | Common:1; Rare:83 | ||||
| chr6:31827508-31827938 | Common:8; Rare:185 | ||||
| chr6:31834538-31835056 | Common:7; Rare:159 | ||||
| chr6:31897652-31897782 | Rare:26 | ||||
| chr6:31901685-31901762 | Rare:12 | ||||
| chr6:31945809-31946096 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr6:31958885-31959204 | Rare:107; Clinvar:8 |