| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159789553-159789993 | Common:4; Rare:150 | ||||
| chr6:161273978-161274172 | Rare:33 | ||||
| chr6:162727733-162728091 | Common:3; Rare:103; Clinvar:1 | ||||
| chr6:163415187-163415347 | Common:1; Rare:48 | ||||
| chr6:163422933-163423207 | Common:3; Rare:52 | ||||
| chr6:166342496-166342665 | Common:3; Rare:67 | ||||
| chr6:166999061-166999424 | Common:1; Rare:122 | ||||
| chr6:167826810-167827138 | Common:2; Rare:183 | ||||
| chr6:169253786-169254104 | Rare:56 | ||||
| chr6:169702004-169702161 | Common:1; Rare:73 | ||||
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306566-170306820 | Common:2; Rare:78 | ||||
| chr6:170553196-170553385 | Common:3; Rare:80 | ||||
| chr6:170554211-170554416 | Common:1; Rare:65 | ||||
| chr6:170584440-170584698 | Common:2; Rare:95 |