| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41072417-41072750 | Rare:91 | ||||
| chr6:41921079-41921237 | Common:1; Rare:43 | ||||
| chr6:42929246-42929550 | Common:3; Rare:82 | ||||
| chr6:43013857-43014314 | Common:2; Rare:106 | ||||
| chr6:43059808-43059913 | Rare:34 | ||||
| chr6:43516739-43517115 | Common:6; Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575975-43576153 | Rare:60 | ||||
| chr6:43629262-43629551 | Common:1; Rare:66 | ||||
| chr6:44127342-44127669 | Common:4; Rare:94 | ||||
| chr6:46652640-46652985 | Common:1; Rare:83 | ||||
| chr6:49463157-49463376 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52577034-52577195 | Common:4; Rare:52 | ||||
| chr6:56843576-56843928 | Common:9; Rare:82 | ||||
| chr6:63572373-63572569 | Rare:71 | ||||
| chr6:73461674-73461829 | Common:1; Rare:57; Clinvar (benign):1 |