| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377865-45378118 | Common:2; Rare:87 | ||||
| chr6:46129774-46130171 | Common:5; Rare:126 | ||||
| chr6:46652718-46653018 | Rare:75 | ||||
| chr6:46921922-46922080 | Rare:39 | ||||
| chr6:47478121-47478225 | Common:1; Rare:35; Clinvar (benign):2 | ||||
| chr6:48068633-48068932 | Common:2; Rare:97 | ||||
| chr6:49463167-49463407 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420124-52420386 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671044-52671175 | Rare:42 | ||||
| chr6:52995266-52995829 | Common:4; Rare:230 | ||||
| chr6:53065379-53065598 | Common:1; Rare:67 | ||||
| chr6:53348889-53349222 | Common:2; Rare:125 | ||||
| chr6:55579014-55579226 | Rare:74 | ||||
| chr6:57046464-57046758 | Rare:101 | ||||
| chr6:57089895-57090225 | Rare:123 |