| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42929226-42929549 | Common:3; Rare:88 | ||||
| chr6:43013878-43014290 | Common:2; Rare:91 | ||||
| chr6:43059818-43059947 | Common:1; Rare:40 | ||||
| chr6:43516730-43517136 | Common:6; Rare:147; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43635747-43635869 | Common:1; Rare:29 | ||||
| chr6:44127369-44127677 | Common:4; Rare:90 | ||||
| chr6:45377795-45378154 | Common:2; Rare:116 | ||||
| chr6:46652779-46653008 | Rare:60 | ||||
| chr6:49463167-49463391 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550453-49550717 | Rare:57 | ||||
| chr6:52576934-52577292 | Common:6; Rare:127 | ||||
| chr6:56542851-56542954 | Common:1; Rare:12 | ||||
| chr6:63572538-63572602 | Rare:22 | ||||
| chr6:70667690-70668066 | Common:4; Rare:140 | ||||
| chr6:75284631-75285056 | Common:1; Rare:134 |