| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112087452-112087667 | Rare:65 | ||||
| chr6:116254068-116254222 | Common:4; Rare:39 | ||||
| chr6:121334462-121334554 | Common:2; Rare:37 | ||||
| chr6:122399386-122399681 | Common:4; Rare:91 | ||||
| chr6:122471779-122471917 | Common:2; Rare:38 | ||||
| chr6:125781060-125781127 | Rare:14 | ||||
| chr6:125986441-125986548 | Rare:41 | ||||
| chr6:127343337-127343669 | Common:2; Rare:73 | ||||
| chr6:128520575-128520791 | Common:1; Rare:81 | ||||
| chr6:129710160-129710282 | Rare:34 | ||||
| chr6:134177843-134178006 | Rare:26 | ||||
| chr6:136289758-136290014 | Common:1; Rare:111 | ||||
| chr6:138692052-138692203 | Common:3; Rare:44 | ||||
| chr6:143060700-143060919 | Common:7; Rare:73 | ||||
| chr6:143450660-143450876 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 |