| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75749087-75749292 | Common:3; Rare:68; Clinvar:3 | ||||
| chr6:78867470-78867593 | Rare:52 | ||||
| chr6:79234564-79234946 | Common:4; Rare:91 | ||||
| chr6:79537346-79537658 | Common:2; Rare:98; Clinvar:4 | ||||
| chr6:80004398-80004697 | Common:6; Rare:72 | ||||
| chr6:81752668-81752837 | Rare:87 | ||||
| chr6:82247704-82247940 | Common:1; Rare:78 | ||||
| chr6:83193194-83193441 | Common:3; Rare:80 | ||||
| chr6:85449905-85450182 | Common:1; Rare:85 | ||||
| chr6:85593720-85593919 | Common:1; Rare:73 | ||||
| chr6:85643796-85643941 | Common:3; Rare:46 | ||||
| chr6:87155268-87155594 | Rare:87 | ||||
| chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702189-87702443 | Common:2; Rare:81 |