| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:13272589-13272772 | Rare:52 | ||||
| chr6:13328483-13328630 | Common:5; Rare:65 | ||||
| chr6:13486142-13486280 | Common:5; Rare:29 | ||||
| chr6:13615170-13615521 | Common:2; Rare:142 | ||||
| chr6:14117535-14117780 | Common:1; Rare:87 | ||||
| chr6:17706407-17706611 | Common:1; Rare:75 | ||||
| chr6:17706736-17707073 | Common:1; Rare:90 | ||||
| chr6:18155355-18155502 | Rare:53 | ||||
| chr6:18264383-18264756 | Common:1; Rare:156 | ||||
| chr6:18387218-18387510 | Common:2; Rare:91 | ||||
| chr6:20401527-20401916 | Common:3; Rare:99 | ||||
| chr6:20534396-20534566 | Common:1; Rare:57 | ||||
| chr6:24495629-24495765 | Common:1; Rare:25 | ||||
| chr6:24522609-24522869 | Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:24666858-24667193 | Common:3; Rare:143 |