| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013838-43014268 | Common:2; Rare:106 | ||||
| chr6:43182115-43182216 | Rare:27 | ||||
| chr6:43229348-43229558 | Rare:71 | ||||
| chr6:43516891-43517109 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576185 | Rare:87; Clinvar:4 | ||||
| chr6:43770085-43770229 | Common:2; Rare:44 | ||||
| chr6:44127278-44127665 | Common:4; Rare:107 | ||||
| chr6:44387449-44387738 | Common:4; Rare:74 | ||||
| chr6:46129805-46130071 | Common:5; Rare:82 | ||||
| chr6:47042330-47042451 | Common:1; Rare:30 | ||||
| chr6:47477629-47478073 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:47478123-47478245 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:49463191-49463417 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420122-52420379 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52670979-52671175 | Rare:64 |