| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32154341-32154513 | Rare:21 | ||||
| chr6:32176054-32176276 | Common:1; Rare:46 | ||||
| chr6:32177047-32177370 | Rare:53 | ||||
| chr6:32178110-32178532 | Common:2; Rare:75 | ||||
| chr6:32189881-32190072 | Common:2; Rare:48 | ||||
| chr6:32190142-32190319 | Rare:37 | ||||
| chr6:32843973-32844130 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844573-32844857 | Common:1; Rare:57 | ||||
| chr6:32853654-32853888 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32853989-32854219 | Common:2; Rare:52 | ||||
| chr6:32968458-32968594 | Common:2; Rare:35 | ||||
| chr6:32968819-32968995 | Common:5; Rare:55 | ||||
| chr6:33075761-33076026 | Common:3; Rare:34 | ||||
| chr6:33200356-33200445 | Rare:22 | ||||
| chr6:33200637-33200952 | Common:3; Rare:93 |