| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44127272-44127671 | Common:4; Rare:111 | ||||
| chr6:44219474-44219725 | Common:2; Rare:69 | ||||
| chr6:44387447-44387771 | Common:4; Rare:86 | ||||
| chr6:46129796-46130062 | Common:5; Rare:83 | ||||
| chr6:46921842-46922053 | Common:2; Rare:57 | ||||
| chr6:47477690-47477949 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:47477969-47478255 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):5 | ||||
| chr6:49463215-49463412 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr6:52420089-52420364 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671061-52671161 | Rare:27 | ||||
| chr6:52995260-52995817 | Common:4; Rare:229 | ||||
| chr6:53348882-53349169 | Common:2; Rare:117 | ||||
| chr6:56542761-56543014 | Common:2; Rare:43 | ||||
| chr6:63572448-63572599 | Rare:55 | ||||
| chr6:63635620-63635865 | Rare:96 |