| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83859566-83859724 | Rare:54 | ||||
| chr6:84764562-84764872 | Common:1; Rare:91 | ||||
| chr6:85593714-85593919 | Common:1; Rare:73 | ||||
| chr6:85643296-85643628 | Common:2; Rare:115 | ||||
| chr6:85643817-85643954 | Common:2; Rare:41 | ||||
| chr6:87155263-87155601 | Rare:89 | ||||
| chr6:87407720-87408054 | Common:1; Rare:70 | ||||
| chr6:87589940-87590180 | Common:3; Rare:117; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702214-87702528 | Common:1; Rare:97 | ||||
| chr6:88963545-88963838 | Common:2; Rare:97 | ||||
| chr6:89117944-89118131 | Common:4; Rare:77 | ||||
| chr6:89562612-89562851 | Common:1; Rare:39 | ||||
| chr6:89638443-89638538 | Common:1; Rare:21 | ||||
| chr6:89638721-89638845 | Common:3; Rare:42 | ||||
| chr6:89819709-89819874 | Rare:56 |