| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170553149-170553220 | Common:1; Rare:25 | ||||
| chr6:170553228-170553343 | Common:1; Rare:54 | ||||
| chr6:170554180-170554440 | Common:1; Rare:78 | ||||
| chr6:170584588-170584811 | Common:1; Rare:69 | ||||
| chr7:192657-192797 | Common:1; Rare:45 | ||||
| chr7:246382-246439 | Common:1; Rare:17; Clinvar (benign):1 | ||||
| chr7:519170-519294 | Rare:33 | ||||
| chr7:727221-727343 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:727589-728006 | Common:1; Rare:91 | ||||
| chr7:876290-876790 | Common:8; Rare:208 | ||||
| chr7:892562-892809 | Common:3; Rare:76 | ||||
| chr7:975485-975654 | Common:1; Rare:80 | ||||
| chr7:1028262-1028537 | Common:2; Rare:105 | ||||
| chr7:1138193-1138475 | Common:2; Rare:85 | ||||
| chr7:1504314-1504434 | Common:1; Rare:61 |