| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31073465-31073912 | Rare:265 | ||||
| chr16:31074135-31074498 | Common:7; Rare:278 | ||||
| chr16:31093041-31093522 | Common:4; Rare:198; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31094531-31095041 | Common:3; Rare:426; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr16:31108260-31108513 | Rare:142 | ||||
| chr16:31117214-31117794 | Common:10; Rare:251 | ||||
| chr16:31117814-31118102 | Rare:163 | ||||
| chr16:31135601-31135845 | Rare:119 | ||||
| chr16:31142172-31142542 | Common:3; Rare:100 | ||||
| chr16:31179807-31180228 | Common:4; Rare:311; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180134-31180264 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180596-31180890 | Common:6; Rare:187 | ||||
| chr16:31202169-31202569 | Common:4; Rare:199 | ||||
| chr16:31202585-31202955 | Common:4; Rare:265 | ||||
| chr16:31215610-31216200 | Common:1; Rare:83 |