| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:80004367-80004697 | Common:10; Rare:128 | ||||
| chr6:80106381-80106719 | Common:2; Rare:119; Clinvar (pathogenic):1 | ||||
| chr6:81752668-81752851 | Rare:188 | ||||
| chr6:82247070-82247500 | Common:3; Rare:131 | ||||
| chr6:82247605-82248009 | Common:2; Rare:217 | ||||
| chr6:83065697-83065973 | Common:1; Rare:98 | ||||
| chr6:83193190-83193467 | Common:6; Rare:167 | ||||
| chr6:85449939-85450144 | Common:2; Rare:120 | ||||
| chr6:85593669-85594064 | Common:3; Rare:235 | ||||
| chr6:85642853-85643050 | Common:4; Rare:153 | ||||
| chr6:85643216-85643564 | Common:1; Rare:253 | ||||
| chr6:85643788-85643964 | Common:6; Rare:101 | ||||
| chr6:87155285-87155639 | Rare:156 | ||||
| chr6:87472832-87473015 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:87589883-87590193 | Common:6; Rare:323; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):4 |