| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:63636013-63636153 | Rare:76 | ||||
| chr6:63636630-63637190 | Common:1; Rare:152 | ||||
| chr6:63806253-63806660 | Rare:121; Clinvar:2 | ||||
| chr6:69796833-69797202 | Common:2; Rare:110; Clinvar:6; Clinvar (benign):3 | ||||
| chr6:70413171-70413580 | Common:4; Rare:238 | ||||
| chr6:70566806-70566986 | Common:2; Rare:121 | ||||
| chr6:70667696-70668015 | Common:6; Rare:214 | ||||
| chr6:71288605-71288861 | Rare:119 | ||||
| chr6:73263181-73263462 | Common:6; Rare:79 | ||||
| chr6:73309590-73310080 | Common:2; Rare:129 | ||||
| chr6:73310097-73310287 | Common:1; Rare:50 | ||||
| chr6:73451613-73452039 | Common:4; Rare:208; Clinvar:2 | ||||
| chr6:73452164-73452422 | Common:2; Rare:70 | ||||
| chr6:73461675-73461996 | Common:2; Rare:158; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:73462070-73462620 | Common:10; Rare:201 |