| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:68714977-68715262 | Common:6; Rare:126 | ||||
| chr18:70205659-70205750 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr18:74148358-74148552 | Common:1; Rare:60 | ||||
| chr18:74291906-74292267 | Common:4; Rare:108 | ||||
| chr18:74499806-74499988 | Common:2; Rare:46 | ||||
| chr18:74597601-74597929 | Common:2; Rare:90 | ||||
| chr18:75208508-75208630 | Common:2; Rare:31 | ||||
| chr18:79988458-79988644 | Common:2; Rare:74; Clinvar (pathogenic):2 | ||||
| chr19:344789-344964 | Common:3; Rare:65 | ||||
| chr19:572237-572661 | Common:3; Rare:211 | ||||
| chr19:633520-633736 | Common:8; Rare:99 | ||||
| chr19:663132-663430 | Common:2; Rare:115 | ||||
| chr19:821940-822077 | Rare:33 | ||||
| chr19:893165-893480 | Common:3; Rare:129 | ||||
| chr19:913160-913274 | Rare:36 |