| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143843189-143843402 | Common:2; Rare:68 | ||||
| chr6:144095524-144095846 | Common:6; Rare:91 | ||||
| chr6:144330725-144330853 | Rare:24 | ||||
| chr6:145814680-145814921 | Common:1; Rare:112 | ||||
| chr6:145964315-145964616 | Rare:101 | ||||
| chr6:149546001-149546191 | Common:1; Rare:82 | ||||
| chr6:149718066-149718153 | Common:1; Rare:29 | ||||
| chr6:149746488-149746615 | Common:2; Rare:62 | ||||
| chr6:149749523-149749796 | Rare:122 | ||||
| chr6:149923071-149923266 | Common:3; Rare:49 | ||||
| chr6:151325566-151325697 | Common:1; Rare:33 | ||||
| chr6:151452016-151452540 | Common:5; Rare:184; Clinvar (benign):3 | ||||
| chr6:152983021-152983260 | Common:2; Rare:75 | ||||
| chr6:152983550-152983715 | Common:3; Rare:58 | ||||
| chr6:153002641-153002838 | Common:3; Rare:71 |