| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149545990-149546155 | Rare:134 | ||||
| chr6:149648584-149648849 | Common:3; Rare:145 | ||||
| chr6:149717705-149717841 | Rare:40 | ||||
| chr6:149718021-149718139 | Common:1; Rare:42 | ||||
| chr6:149718044-149718193 | Common:3; Rare:53 | ||||
| chr6:149746468-149746664 | Common:6; Rare:182 | ||||
| chr6:149749573-149749872 | Rare:263 | ||||
| chr6:149750220-149750670 | Common:2; Rare:106 | ||||
| chr6:149864261-149864475 | Common:6; Rare:137 | ||||
| chr6:150865580-150865804 | Common:2; Rare:106 | ||||
| chr6:150866190-150866650 | Common:2; Rare:159 | ||||
| chr6:151390870-151391230 | Common:5; Rare:150 | ||||
| chr6:151391506-151391764 | Common:6; Rare:120 | ||||
| chr6:151391790-151392297 | Common:4; Rare:189 | ||||
| chr6:151452008-151452577 | Common:10; Rare:390; Clinvar (benign):6 |