| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32177042-32177182 | Rare:25 | ||||
| chr6:32177292-32177482 | Common:2; Rare:31 | ||||
| chr6:32178085-32178648 | Common:3; Rare:116 | ||||
| chr6:32190145-32190433 | Rare:55 | ||||
| chr6:32853690-32853819 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32854019-32854200 | Common:2; Rare:47 | ||||
| chr6:32968502-32968609 | Common:1; Rare:29 | ||||
| chr6:32969068-32969360 | Common:5; Rare:86 | ||||
| chr6:32970739-32970952 | Common:1; Rare:59 | ||||
| chr6:32976396-32976609 | Rare:81 | ||||
| chr6:33200337-33200449 | Rare:32 | ||||
| chr6:33200654-33200952 | Common:3; Rare:89 | ||||
| chr6:33208443-33208533 | Rare:23 | ||||
| chr6:33271639-33272126 | Common:3; Rare:174 | ||||
| chr6:33289186-33289383 | Common:1; Rare:50 |