| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197434892-197435327 | Rare:664 | ||||
| chr2:197435421-197435821 | Common:2; Rare:48 | ||||
| chr2:197453070-197453603 | Rare:921 | ||||
| chr2:197453809-197454446 | Common:7; Rare:408 | ||||
| chr2:197499161-197499562 | Common:1; Rare:166 | ||||
| chr2:197499754-197500630 | Common:9; Rare:1684; Clinvar:7; Clinvar (benign):11 | ||||
| chr2:197514631-197516122 | Common:9; Rare:839 | ||||
| chr2:197705098-197705498 | Common:18; Rare:886; Clinvar:6; Clinvar (benign):13 | ||||
| chr2:197804232-197804787 | Common:11; Rare:657 | ||||
| chr2:197804751-197805151 | Common:4; Rare:100 | ||||
| chr2:197805099-197805499 | Common:2; Rare:83 | ||||
| chr2:197810555-197810955 | Common:10; Rare:130 | ||||
| chr2:199455600-199455926 | Rare:148; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:199455896-199456324 | Rare:381; Clinvar (benign):3 | ||||
| chr2:199456762-199457186 | Common:12; Rare:276 |