| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53348882-53349120 | Common:2; Rare:101 | ||||
| chr6:56851814-56852022 | Rare:37 | ||||
| chr6:56852097-56852355 | Rare:28 | ||||
| chr6:57046503-57046738 | Rare:82 | ||||
| chr6:57222260-57222419 | Rare:62 | ||||
| chr6:63572229-63572622 | Rare:145 | ||||
| chr6:69796883-69797135 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70413174-70413545 | Common:2; Rare:114 | ||||
| chr6:70566653-70566958 | Common:2; Rare:74 | ||||
| chr6:70667696-70667964 | Common:2; Rare:92 | ||||
| chr6:73520991-73521349 | Common:3; Rare:97 | ||||
| chr6:73521555-73521655 | Rare:27 | ||||
| chr6:73653966-73654146 | Common:2; Rare:46; Clinvar:2 | ||||
| chr6:75243745-75243963 | Common:1; Rare:96 | ||||
| chr6:75284749-75285033 | Common:1; Rare:80 |