| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30763543-30763754 | Common:13; Rare:49 | ||||
| chr6:30763970-30764590 | Common:5; Rare:114 | ||||
| chr6:30769110-30769540 | Rare:123 | ||||
| chr6:30781560-30782142 | Common:7; Rare:115 | ||||
| chr6:30815523-30815686 | Common:4; Rare:45 | ||||
| chr6:31186078-31186234 | Common:11; Rare:69 | ||||
| chr6:31400594-31400731 | Common:4; Rare:28 | ||||
| chr6:31494154-31494307 | Common:11; Rare:13 | ||||
| chr6:31649196-31649826 | Rare:344 | ||||
| chr6:31656196-31656619 | Common:2; Rare:134 | ||||
| chr6:31733905-31734144 | Rare:77 | ||||
| chr6:31734611-31735011 | Common:3; Rare:108 | ||||
| chr6:31821870-31822250 | Common:4; Rare:108 | ||||
| chr6:31865221-31865750 | Common:1; Rare:256 | ||||
| chr6:32048366-32049100 | Common:7; Rare:244; Clinvar:1; Clinvar (pathogenic):2 |