| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568714-218568935 | Common:1; Rare:56 | ||||
| chr2:218659317-218659762 | Common:4; Rare:109 | ||||
| chr2:218671975-218672334 | Common:2; Rare:89 | ||||
| chr2:218782026-218782185 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:219176893-219177098 | Common:4; Rare:63 | ||||
| chr2:219178142-219178355 | Common:6; Rare:111 | ||||
| chr2:219206683-219206923 | Rare:87 | ||||
| chr2:219229336-219229422 | Rare:28 | ||||
| chr2:219229535-219229900 | Common:2; Rare:116 | ||||
| chr2:219245416-219245542 | Common:1; Rare:39 | ||||
| chr2:219253874-219254056 | Common:1; Rare:57 | ||||
| chr2:219279272-219279545 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr2:219309362-219309553 | Rare:56 | ||||
| chr2:219387596-219387650 | Rare:10 | ||||
| chr2:219418347-219419054 | Common:6; Rare:232; Clinvar:40; Clinvar (benign):24; Clinvar (pathogenic):3 |