| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49463151-49463376 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49787289-49787439 | Common:1; Rare:36 | ||||
| chr6:52284682-52285041 | Common:2; Rare:128 | ||||
| chr6:52420240-52420364 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52577016-52577260 | Common:4; Rare:87 | ||||
| chr6:52670986-52671187 | Rare:65 | ||||
| chr6:52995255-52995823 | Common:4; Rare:230 | ||||
| chr6:53065377-53065672 | Common:1; Rare:83 | ||||
| chr6:53348399-53348578 | Common:1; Rare:53 | ||||
| chr6:53348871-53349015 | Common:1; Rare:79 | ||||
| chr6:53349098-53349170 | Rare:22 | ||||
| chr6:53349199-53349248 | Rare:11 | ||||
| chr6:53545097-53545239 | Rare:41 | ||||
| chr6:54846444-54846786 | Common:2; Rare:83 | ||||
| chr6:56542802-56542946 | Common:1; Rare:23 |