| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9423371-9423707 | Rare:102 | ||||
| chr2:9473602-9473782 | Common:1; Rare:42 | ||||
| chr2:9474493-9474642 | Common:6; Rare:71 | ||||
| chr2:9555615-9555966 | Common:2; Rare:117 | ||||
| chr2:9843240-9843539 | Common:6; Rare:90 | ||||
| chr2:10689925-10690038 | Common:2; Rare:34 | ||||
| chr2:11466127-11466230 | Common:2; Rare:30 | ||||
| chr2:11482673-11482895 | Common:2; Rare:62 | ||||
| chr2:11539754-11540071 | Common:5; Rare:45 | ||||
| chr2:11746422-11746671 | Common:2; Rare:73; Clinvar:4 | ||||
| chr2:12716614-12717053 | Common:3; Rare:139 | ||||
| chr2:17518434-17518638 | Common:2; Rare:56 | ||||
| chr2:17753721-17753914 | Common:2; Rare:71 | ||||
| chr2:17754062-17754159 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr2:19901667-19901759 | Common:1; Rare:46 |