| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83067330-83067778 | Common:2; Rare:95 | ||||
| chr6:83068018-83068144 | Common:1; Rare:28 | ||||
| chr6:83193222-83193407 | Common:3; Rare:67 | ||||
| chr6:85449939-85450140 | Common:1; Rare:59 | ||||
| chr6:85593693-85593975 | Common:1; Rare:97 | ||||
| chr6:85643812-85643931 | Common:2; Rare:37 | ||||
| chr6:87155263-87155631 | Rare:107 | ||||
| chr6:87472847-87473012 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):4 | ||||
| chr6:87589915-87590165 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87701548-87701601 | Common:1; Rare:14 | ||||
| chr6:87701673-87701965 | Common:2; Rare:102 | ||||
| chr6:87702178-87702441 | Common:2; Rare:83 | ||||
| chr6:89081045-89081397 | Common:2; Rare:135 | ||||
| chr6:89145989-89146117 | Rare:39 | ||||
| chr6:89352589-89353039 | Common:4; Rare:113 |