| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202280532-202280815 | Common:3; Rare:62 | ||||
| chr2:202376066-202376377 | Rare:126 | ||||
| chr2:202453148-202453189 | Rare:7 | ||||
| chr2:202514971-202515269 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr2:202530155-202530379 | Rare:36 | ||||
| chr2:202539129-202539410 | Rare:34 | ||||
| chr2:202542141-202542337 | Rare:55; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:202619958-202619972 | Rare:3 | ||||
| chr2:202861606-202861877 | Common:2; Rare:42 | ||||
| chr2:203123334-203123522 | Common:2; Rare:27 | ||||
| chr2:203126676-203126926 | Common:1; Rare:70 | ||||
| chr2:203144843-203145152 | Rare:112 | ||||
| chr2:203175059-203175245 | Rare:49 | ||||
| chr2:203203965-203204070 | Rare:22 | ||||
| chr2:203220504-203220815 | Rare:50 |