| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85593734-85593975 | Common:1; Rare:83 | ||||
| chr6:85643817-85643905 | Common:2; Rare:30 | ||||
| chr6:87155268-87155615 | Rare:97 | ||||
| chr6:87472918-87473006 | Common:1; Rare:35; Clinvar (benign):4 | ||||
| chr6:87589940-87590171 | Common:3; Rare:111; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702228-87702481 | Common:1; Rare:75 | ||||
| chr6:88963561-88963826 | Common:2; Rare:91 | ||||
| chr6:89080581-89080784 | Common:1; Rare:89 | ||||
| chr6:89081257-89081335 | Rare:27 | ||||
| chr6:89638434-89638549 | Common:1; Rare:25 | ||||
| chr6:89638713-89638845 | Common:3; Rare:47 | ||||
| chr6:89819768-89819918 | Rare:44 | ||||
| chr6:89829603-89829914 | Rare:71 | ||||
| chr6:90586991-90587384 | Common:5; Rare:111 | ||||
| chr6:93419552-93419824 | Common:1; Rare:73 |