| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96837376-96837540 | Common:4; Rare:63 | ||||
| chr6:96837581-96837642 | Rare:15 | ||||
| chr6:96897692-96898101 | Common:4; Rare:148; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:96924321-96924795 | Common:4; Rare:116 | ||||
| chr6:97283095-97283421 | Common:3; Rare:88 | ||||
| chr6:98834358-98834583 | Common:1; Rare:61 | ||||
| chr6:98947824-98948216 | Common:2; Rare:102 | ||||
| chr6:99350023-99350076 | Rare:16 | ||||
| chr6:99393895-99394068 | Common:1; Rare:72 | ||||
| chr6:99424614-99424986 | Common:1; Rare:99 | ||||
| chr6:99425214-99425532 | Common:2; Rare:92 | ||||
| chr6:99515400-99515562 | Common:1; Rare:54 | ||||
| chr6:100881193-100881522 | Common:6; Rare:117 | ||||
| chr6:104859707-104860010 | Common:1; Rare:90 | ||||
| chr6:104956989-104957194 | Rare:33 |