| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25673459-25673744 | Common:1; Rare:105 | ||||
| chr2:25878445-25878759 | Common:3; Rare:97 | ||||
| chr2:26033776-26034230 | Common:4; Rare:167 | ||||
| chr2:26034339-26034732 | Common:2; Rare:93 | ||||
| chr2:26194568-26194820 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244083-26244426 | Common:1; Rare:64 | ||||
| chr2:26244564-26244984 | Common:2; Rare:156; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345789-26346160 | Common:1; Rare:111 | ||||
| chr2:26764188-26764369 | Common:2; Rare:67 | ||||
| chr2:27032812-27033009 | Rare:76 | ||||
| chr2:27071551-27071878 | Common:1; Rare:98 | ||||
| chr2:27078996-27079153 | Common:1; Rare:57; Clinvar:1 | ||||
| chr2:27086537-27086784 | Common:2; Rare:73 | ||||
| chr2:27134615-27134779 | Common:1; Rare:69 | ||||
| chr2:27211775-27212109 | Common:3; Rare:117 |