| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219278960-219280374 | Common:21; Rare:1386; Clinvar:3; Clinvar (benign):16 | ||||
| chr2:219295403-219296492 | Common:15; Rare:574 | ||||
| chr2:219387350-219387484 | Rare:43 | ||||
| chr2:219387770-219389026 | Common:11; Rare:662 | ||||
| chr2:219419780-219420180 | Common:5; Rare:249; Clinvar:14; Clinvar (benign):10; Clinvar (pathogenic):5 | ||||
| chr2:219433950-219434350 | Common:1; Rare:78 | ||||
| chr2:219441790-219442190 | Rare:184 | ||||
| chr2:219459659-219461010 | Common:20; Rare:508 | ||||
| chr2:219461151-219461551 | Common:1; Rare:129 | ||||
| chr2:219497799-219498199 | Common:11; Rare:385 | ||||
| chr2:219498382-219498981 | Common:22; Rare:675 | ||||
| chr2:219500162-219500604 | Common:1; Rare:165; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:219514132-219514941 | Common:11; Rare:837 | ||||
| chr2:219516949-219517377 | Common:2; Rare:252 | ||||
| chr2:219542630-219543030 | Common:3; Rare:72 |