| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7541366-7541696 | Common:1; Rare:99; Clinvar (benign):1 | ||||
| chr6:7910633-7910910 | Common:3; Rare:106 | ||||
| chr6:8102517-8102740 | Common:1; Rare:71 | ||||
| chr6:8435472-8435654 | Common:4; Rare:72 | ||||
| chr6:10521213-10521370 | Rare:39 | ||||
| chr6:10694595-10694994 | Common:5; Rare:108 | ||||
| chr6:10747630-10747875 | Common:2; Rare:98 | ||||
| chr6:11094061-11094270 | Rare:59 | ||||
| chr6:11232553-11232832 | Rare:69 | ||||
| chr6:12290089-12290598 | Common:1; Rare:109 | ||||
| chr6:13328509-13328746 | Common:4; Rare:78 | ||||
| chr6:13487575-13487808 | Common:1; Rare:65 | ||||
| chr6:13615180-13615553 | Common:2; Rare:146 | ||||
| chr6:13924928-13924993 | Rare:22 | ||||
| chr6:17600128-17600401 | Common:5; Rare:90 |