| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31665854-31666152 | Common:3; Rare:83 | ||||
| chr6:31714045-31714177 | Common:1; Rare:15 | ||||
| chr6:31729486-31729573 | Rare:14 | ||||
| chr6:31730052-31730339 | Common:2; Rare:73 | ||||
| chr6:31739751-31740020 | Common:2; Rare:63 | ||||
| chr6:31806789-31807039 | Common:1; Rare:96 | ||||
| chr6:31815285-31815550 | Common:1; Rare:79 | ||||
| chr6:31827275-31827298 | Rare:6 | ||||
| chr6:31827517-31827746 | Common:2; Rare:72 | ||||
| chr6:31834618-31834929 | Common:3; Rare:69 | ||||
| chr6:31862772-31863112 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31897646-31897782 | Rare:28 | ||||
| chr6:31945800-31946094 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr6:31958899-31959184 | Rare:87; Clinvar:8 | ||||
| chr6:32128203-32128393 | Common:2; Rare:40 |