| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32130264-32130378 | Rare:18 | ||||
| chr6:32154749-32155047 | Rare:60 | ||||
| chr6:32164483-32164643 | Rare:21 | ||||
| chr6:32176054-32176251 | Common:1; Rare:40 | ||||
| chr6:32178078-32178604 | Common:3; Rare:105 | ||||
| chr6:32178811-32178959 | Common:3; Rare:24 | ||||
| chr6:32190146-32190316 | Rare:34 | ||||
| chr6:32666636-32666859 | Common:31; Rare:23 | ||||
| chr6:32844002-32844119 | Rare:26; Clinvar:1 | ||||
| chr6:32844622-32844848 | Common:1; Rare:49 | ||||
| chr6:32853685-32853754 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32854023-32854209 | Common:2; Rare:48 | ||||
| chr6:32940956-32941144 | Common:1; Rare:36 | ||||
| chr6:32970739-32970970 | Common:1; Rare:62 | ||||
| chr6:33075781-33075997 | Common:3; Rare:24 |