| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116253765-116254284 | Common:11; Rare:174 | ||||
| chr6:116279099-116279815 | Common:5; Rare:268 | ||||
| chr6:116279822-116280187 | Common:3; Rare:113 | ||||
| chr6:116370734-116371028 | Common:1; Rare:76 | ||||
| chr6:116571157-116571618 | Common:3; Rare:135 | ||||
| chr6:116616257-116616509 | Common:3; Rare:52 | ||||
| chr6:116681056-116681296 | Common:4; Rare:69 | ||||
| chr6:116877130-116877290 | Common:3; Rare:59 | ||||
| chr6:117453745-117453849 | Rare:17 | ||||
| chr6:117482663-117482879 | Rare:66 | ||||
| chr6:117573530-117573823 | Rare:55 | ||||
| chr6:117602185-117602648 | Common:4; Rare:145 | ||||
| chr6:117675270-117675505 | Common:3; Rare:62 | ||||
| chr6:118548189-118548328 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118651461-118651737 | Common:4; Rare:86 |