| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32177071-32177221 | Rare:28 | ||||
| chr6:32177452-32177745 | Common:1; Rare:51 | ||||
| chr6:32178102-32178412 | Common:2; Rare:43 | ||||
| chr6:32190146-32190346 | Rare:37 | ||||
| chr6:32224052-32224334 | Common:2; Rare:50 | ||||
| chr6:32530222-32530442 | Common:16; Rare:30 | ||||
| chr6:32844001-32844099 | Rare:24; Clinvar:1 | ||||
| chr6:32844598-32844848 | Common:1; Rare:53 | ||||
| chr6:32853660-32853888 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:32854023-32854216 | Common:2; Rare:49 | ||||
| chr6:32968477-32968609 | Common:2; Rare:39 | ||||
| chr6:32970851-32970952 | Common:1; Rare:30 | ||||
| chr6:33075795-33076009 | Common:2; Rare:23 | ||||
| chr6:33200652-33200938 | Common:2; Rare:85 | ||||
| chr6:33208436-33208551 | Rare:30 |