| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79552279-79552436 | Common:1; Rare:26 | ||||
| chr6:80307427-80307698 | Common:5; Rare:39 | ||||
| chr6:81736559-81736709 | Rare:19 | ||||
| chr6:81753304-81753502 | Common:1; Rare:74 | ||||
| chr6:83124024-83124223 | Rare:30 | ||||
| chr6:84190297-84190398 | Rare:24 | ||||
| chr6:84689298-84689481 | Rare:31 | ||||
| chr6:84773721-84773808 | Common:2; Rare:31 | ||||
| chr6:85326878-85327036 | Common:1; Rare:36 | ||||
| chr6:85578149-85578481 | Rare:55 | ||||
| chr6:85678708-85679086 | Rare:125 | ||||
| chr6:85865683-85865888 | Common:1; Rare:57 | ||||
| chr6:87010539-87010629 | Rare:17 | ||||
| chr6:87122478-87122576 | Rare:35 | ||||
| chr6:87520197-87520507 | Common:1; Rare:79; Clinvar:1; Clinvar (pathogenic):1 |