| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75601771-75601904 | Rare:50 | ||||
| chr6:75749120-75749251 | Common:3; Rare:34; Clinvar:2 | ||||
| chr6:78867481-78867554 | Rare:26 | ||||
| chr6:79537327-79537602 | Common:2; Rare:78; Clinvar:4 | ||||
| chr6:83193201-83193391 | Common:3; Rare:63 | ||||
| chr6:84763454-84763631 | Rare:42 | ||||
| chr6:84764569-84764758 | Rare:57 | ||||
| chr6:85449939-85450150 | Common:1; Rare:63 | ||||
| chr6:85643817-85643918 | Common:2; Rare:33 | ||||
| chr6:87155268-87155614 | Rare:96 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:89638721-89638806 | Common:3; Rare:29 | ||||
| chr6:90587007-90587334 | Common:3; Rare:91 | ||||
| chr6:95577408-95577543 | Common:3; Rare:36 | ||||
| chr6:96897817-96898083 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 |