| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1971759-1972156 | Common:3; Rare:114 | ||||
| chr16:1972435-1972703 | Common:1; Rare:63 | ||||
| chr16:1979274-1979543 | Common:1; Rare:153 | ||||
| chr16:1979704-1979935 | Common:2; Rare:86 | ||||
| chr16:1983522-1983722 | Common:1; Rare:57 | ||||
| chr16:1983876-1984309 | Common:6; Rare:132; Clinvar (benign):4 | ||||
| chr16:1984388-1984462 | Rare:26; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:1984579-1984636 | Rare:13 | ||||
| chr16:1984808-1984861 | Rare:17 | ||||
| chr16:2009678-2010045 | Common:17; Rare:151 | ||||
| chr16:2010250-2010463 | Common:1; Rare:54 | ||||
| chr16:2026795-2026929 | Common:1; Rare:47 | ||||
| chr16:2047767-2048068 | Rare:152; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr16:2072234-2072323 | Rare:31; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr16:2135356-2135573 | Rare:66; Clinvar:1; Clinvar (benign):2 |