| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844000-32844126 | Rare:27; Clinvar:1 | ||||
| chr6:32844339-32844447 | Rare:28 | ||||
| chr6:32844565-32844840 | Common:1; Rare:55 | ||||
| chr6:32853660-32853888 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:32854028-32854227 | Common:2; Rare:53 | ||||
| chr6:33200656-33200932 | Common:2; Rare:83 | ||||
| chr6:33208300-33208524 | Common:1; Rare:51 | ||||
| chr6:33271842-33272113 | Common:1; Rare:110 | ||||
| chr6:33288995-33289302 | Common:1; Rare:107 | ||||
| chr6:33298930-33299051 | Rare:31 | ||||
| chr6:34248984-34249273 | Common:1; Rare:69 | ||||
| chr6:34757330-34757541 | Common:1; Rare:62 | ||||
| chr6:39115080-39115250 | Common:1; Rare:57 | ||||
| chr6:41921111-41921192 | Rare:20 | ||||
| chr6:42929226-42929550 | Common:3; Rare:88 |