| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844002-32844130 | Rare:28; Clinvar:1 | ||||
| chr6:32844622-32844848 | Common:1; Rare:49 | ||||
| chr6:32853690-32853777 | Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32854022-32854216 | Common:2; Rare:50 | ||||
| chr6:32970851-32970952 | Common:1; Rare:30 | ||||
| chr6:32976396-32976646 | Rare:101 | ||||
| chr6:33200656-33200938 | Common:2; Rare:85 | ||||
| chr6:33208436-33208536 | Rare:24 | ||||
| chr6:33271639-33272148 | Common:4; Rare:182 | ||||
| chr6:33289198-33289307 | Common:1; Rare:28 | ||||
| chr6:33289507-33289646 | Rare:32 | ||||
| chr6:33298908-33299091 | Rare:46 | ||||
| chr6:33299408-33299510 | Common:1; Rare:23 | ||||
| chr6:33314197-33314525 | Common:4; Rare:48 | ||||
| chr6:33391547-33391923 | Common:3; Rare:86 |