| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44127351-44127663 | Common:4; Rare:91 | ||||
| chr6:44246904-44247193 | Common:4; Rare:121 | ||||
| chr6:44387452-44387844 | Common:4; Rare:106 | ||||
| chr6:45377810-45378183 | Common:2; Rare:122 | ||||
| chr6:46129772-46130076 | Common:5; Rare:94 | ||||
| chr6:46652654-46653017 | Common:1; Rare:87 | ||||
| chr6:47477625-47477981 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478103-47478247 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:49463101-49463434 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52420122-52420398 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995266-52995817 | Common:4; Rare:228 | ||||
| chr6:53065369-53065603 | Common:1; Rare:72 | ||||
| chr6:53065705-53065791 | Rare:28 | ||||
| chr6:53348847-53349248 | Common:2; Rare:162 | ||||
| chr6:53616243-53616507 | Common:4; Rare:52 |