| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:35259395-35259547 | Rare:47 | ||||
| chr6:35921047-35921178 | Rare:68 | ||||
| chr6:36678415-36678801 | Common:1; Rare:94 | ||||
| chr6:36874765-36874889 | Rare:47 | ||||
| chr6:37257594-37257799 | Rare:47 | ||||
| chr6:37433168-37433274 | Common:2; Rare:31 | ||||
| chr6:41072633-41073005 | Rare:107 | ||||
| chr6:41921085-41921229 | Common:1; Rare:38 | ||||
| chr6:42452024-42452357 | Common:2; Rare:62 | ||||
| chr6:42929231-42929549 | Common:3; Rare:86 | ||||
| chr6:43013901-43014329 | Common:1; Rare:90 | ||||
| chr6:43021596-43021697 | Rare:49 | ||||
| chr6:43059820-43059913 | Rare:31 | ||||
| chr6:43516800-43517109 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575939-43576153 | Rare:79 |