| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165953748-165953851 | Common:1; Rare:49; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:166375867-166376258 | Common:5; Rare:109; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166494121-166494328 | Common:1; Rare:33 | ||||
| chr2:169362504-169362688 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169573740-169574017 | Common:2; Rare:77 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584709-169584811 | Rare:26 | ||||
| chr2:169694335-169694590 | Common:5; Rare:90 | ||||
| chr2:169798739-169798965 | Rare:62 | ||||
| chr2:170715722-170715908 | Common:1; Rare:53 | ||||
| chr2:170817189-170817286 | Common:5; Rare:22 | ||||
| chr2:170821509-170821709 | Rare:37 | ||||
| chr2:170928899-170929318 | Common:5; Rare:118 | ||||
| chr2:171160340-171160574 | Rare:84 | ||||
| chr2:171433991-171434248 | Common:1; Rare:66 |