| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53616561-53616756 | Common:1; Rare:35 | ||||
| chr6:53616909-53617129 | Common:2; Rare:35 | ||||
| chr6:53617134-53617199 | Common:1; Rare:10 | ||||
| chr6:56542790-56542999 | Common:1; Rare:34 | ||||
| chr6:56692605-56692760 | Common:1; Rare:44 | ||||
| chr6:56692795-56692877 | Rare:24 | ||||
| chr6:56693091-56693518 | Rare:76 | ||||
| chr6:56843157-56843268 | Rare:37 | ||||
| chr6:57172568-57172809 | Common:1; Rare:73 | ||||
| chr6:63521622-63521785 | Rare:30 | ||||
| chr6:63571757-63572068 | Rare:62 | ||||
| chr6:63572270-63572718 | Rare:149 | ||||
| chr6:63635793-63636132 | Common:1; Rare:109 | ||||
| chr6:63806291-63806613 | Rare:59; Clinvar:1 | ||||
| chr6:69796847-69797142 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):3 |