| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770085-43770230 | Common:2; Rare:44 | ||||
| chr6:44127351-44127675 | Common:4; Rare:95 | ||||
| chr6:44223445-44223615 | Common:1; Rare:49 | ||||
| chr6:44246854-44247179 | Common:5; Rare:137 | ||||
| chr6:44257492-44257689 | Rare:52 | ||||
| chr6:44387445-44387753 | Common:4; Rare:82 | ||||
| chr6:45377798-45378189 | Common:2; Rare:128 | ||||
| chr6:46129788-46130076 | Common:5; Rare:90 | ||||
| chr6:47478073-47478255 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463178-49463453 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550462-49550746 | Rare:63 | ||||
| chr6:52284670-52284898 | Common:1; Rare:94 | ||||
| chr6:52420101-52420383 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52670992-52671163 | Rare:51 | ||||
| chr6:52995267-52995794 | Common:4; Rare:220 |