| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:234308765-234309000 | Common:1; Rare:42 | ||||
| chr2:236718804-236718905 | Rare:15 | ||||
| chr2:236976287-236976550 | Common:5; Rare:40 | ||||
| chr2:236989056-236989166 | Common:1; Rare:24 | ||||
| chr2:237359054-237359222 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:237691187-237691252 | Rare:10 | ||||
| chr2:239267430-239267637 | Rare:47 | ||||
| chr2:239280224-239280425 | Common:2; Rare:41 | ||||
| chr2:239381030-239381165 | Common:2; Rare:28 | ||||
| chr2:239501329-239501494 | Common:1; Rare:32 | ||||
| chr2:239978497-239978722 | Common:2; Rare:48 | ||||
| chr2:240584817-240584905 | Common:1; Rare:21 | ||||
| chr2:240960893-240961207 | Common:2; Rare:44 | ||||
| chr2:240962262-240962547 | Common:2; Rare:65 | ||||
| chr2:240963113-240963127 | Rare:1 |