| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31878968-31879114 | Common:1; Rare:37 | ||||
| chr6:31897654-31897782 | Rare:25 | ||||
| chr6:31958899-31959198 | Rare:99; Clinvar:8 | ||||
| chr6:32153757-32154241 | Common:4; Rare:83 | ||||
| chr6:32154328-32154498 | Rare:23 | ||||
| chr6:32176054-32176190 | Rare:29 | ||||
| chr6:32178125-32178611 | Common:2; Rare:100 | ||||
| chr6:32190146-32190346 | Rare:37 | ||||
| chr6:32844002-32844119 | Rare:26; Clinvar:1 | ||||
| chr6:32844374-32844546 | Rare:44 | ||||
| chr6:32844604-32844849 | Common:1; Rare:53 | ||||
| chr6:32853670-32853832 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853984-32854204 | Common:2; Rare:52 | ||||
| chr6:32968461-32968607 | Common:2; Rare:40 | ||||
| chr6:33200356-33200445 | Rare:22 |