| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44387435-44387747 | Common:4; Rare:81 | ||||
| chr6:45377628-45377718 | Common:1; Rare:37 | ||||
| chr6:45377782-45378215 | Common:2; Rare:137 | ||||
| chr6:46129774-46130171 | Common:5; Rare:126 | ||||
| chr6:46170896-46171238 | Common:2; Rare:86 | ||||
| chr6:46652718-46653014 | Rare:74 | ||||
| chr6:47477619-47478023 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478033-47478253 | Common:3; Rare:75; Clinvar:4; Clinvar (benign):4 | ||||
| chr6:49463122-49463430 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52284676-52284811 | Common:1; Rare:64 | ||||
| chr6:52420136-52420386 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576992-52577292 | Common:5; Rare:111 | ||||
| chr6:52671054-52671167 | Rare:30 | ||||
| chr6:52995266-52995812 | Common:4; Rare:227 | ||||
| chr6:53061666-53061977 | Rare:70 |