| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:20320022-20320090 | Common:2; Rare:40 | ||||
| chr6:20402961-20403093 | Rare:39 | ||||
| chr6:20404650-20404789 | Common:2; Rare:35 | ||||
| chr6:20427969-20428239 | Common:1; Rare:48 | ||||
| chr6:20688850-20688985 | Rare:19 | ||||
| chr6:20877503-20877779 | Common:2; Rare:46 | ||||
| chr6:21438313-21438408 | Rare:17 | ||||
| chr6:21438618-21438770 | Common:1; Rare:25 | ||||
| chr6:21587852-21587998 | Rare:29 | ||||
| chr6:21588853-21589092 | Common:2; Rare:46 | ||||
| chr6:21593521-21593882 | Common:1; Rare:93 | ||||
| chr6:21594215-21594409 | Common:1; Rare:57 | ||||
| chr6:21594473-21594898 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr6:21596789-21596837 | Rare:11 | ||||
| chr6:22025341-22025455 | Common:1; Rare:14 |