| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46652718-46653013 | Rare:74 | ||||
| chr6:46687829-46687945 | Common:1; Rare:38 | ||||
| chr6:46921922-46922053 | Rare:32 | ||||
| chr6:47309892-47310111 | Common:1; Rare:56 | ||||
| chr6:47477619-47478253 | Common:5; Rare:184; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:47786924-47787156 | Common:1; Rare:36 | ||||
| chr6:49463143-49463431 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550480-49550752 | Rare:60 | ||||
| chr6:49551295-49551460 | Common:1; Rare:64 | ||||
| chr6:49713394-49713693 | Common:4; Rare:80 | ||||
| chr6:49787045-49787456 | Common:1; Rare:118 | ||||
| chr6:52284682-52285041 | Common:2; Rare:128 | ||||
| chr6:52420122-52420392 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576987-52577292 | Common:5; Rare:114 | ||||
| chr6:52577309-52577474 | Common:1; Rare:54 |