| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31806807-31807044 | Common:1; Rare:88 | ||||
| chr6:31827516-31827797 | Common:5; Rare:108 | ||||
| chr6:31862813-31862871 | Common:1; Rare:18; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31897667-31897782 | Rare:21 | ||||
| chr6:31958892-31959184 | Rare:89; Clinvar:8 | ||||
| chr6:31972507-31972606 | Common:1; Rare:32 | ||||
| chr6:32128186-32128460 | Common:2; Rare:73 | ||||
| chr6:32190169-32190382 | Rare:37 | ||||
| chr6:32192598-32192699 | Rare:15 | ||||
| chr6:32192863-32192989 | Common:1; Rare:14 | ||||
| chr6:32530225-32530483 | Common:19; Rare:31 | ||||
| chr6:32589733-32590080 | Common:24; Rare:30 | ||||
| chr6:32637274-32637445 | Common:17; Rare:15 | ||||
| chr6:32666636-32666910 | Common:42; Rare:24 | ||||
| chr6:32816997-32817158 | Common:1; Rare:27 |