| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50582537-50582923 | Common:7; Rare:158; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr22:50582928-50583240 | Common:4; Rare:102 | ||||
| chr22:50628021-50628410 | Common:9; Rare:157; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783597-50783822 | Common:2; Rare:74 | ||||
| chr22:50784098-50784267 | Rare:23 | ||||
| chr3:196458-196814 | Common:1; Rare:94 | ||||
| chr3:197003-197348 | Common:3; Rare:119 | ||||
| chr3:198002-198059 | Common:1; Rare:10 | ||||
| chr3:3126651-3127227 | Common:10; Rare:219; Clinvar (benign):4 | ||||
| chr3:3179636-3179877 | Common:2; Rare:98; Clinvar:4 | ||||
| chr3:4303247-4303426 | Common:2; Rare:70 | ||||
| chr3:4303478-4303700 | Common:2; Rare:83 | ||||
| chr3:4466962-4467372 | Common:2; Rare:181; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:4493094-4493553 | Common:2; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:4978544-4978938 | Common:4; Rare:121 |