| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32177047-32177177 | Rare:23 | ||||
| chr6:32190125-32190344 | Rare:44 | ||||
| chr6:32530250-32530480 | Common:17; Rare:15 | ||||
| chr6:32844002-32844149 | Rare:32; Clinvar:1 | ||||
| chr6:32844342-32844441 | Rare:24 | ||||
| chr6:32844622-32844840 | Common:1; Rare:47 | ||||
| chr6:32853670-32853968 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853989-32854216 | Common:2; Rare:52 | ||||
| chr6:32968502-32968607 | Common:1; Rare:28 | ||||
| chr6:32968819-32968924 | Common:4; Rare:34 | ||||
| chr6:32970721-32970952 | Common:1; Rare:63 | ||||
| chr6:32976365-32976633 | Rare:99 | ||||
| chr6:32977529-32977893 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr6:33075713-33075998 | Common:5; Rare:35 | ||||
| chr6:33200356-33200445 | Rare:22 |