| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89490713-89490924 | Common:3; Rare:59 | ||||
| chr16:89508325-89508492 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560537-89560717 | Rare:75 | ||||
| chr16:89657584-89658145 | Common:5; Rare:276; Clinvar (benign):1 | ||||
| chr16:89686567-89686728 | Common:8; Rare:78 | ||||
| chr16:89686898-89686960 | Rare:24 | ||||
| chr16:89687361-89687556 | Rare:72 | ||||
| chr16:89701687-89701848 | Rare:64 | ||||
| chr16:89711598-89711896 | Common:3; Rare:109 | ||||
| chr16:89720857-89720979 | Common:1; Rare:32 | ||||
| chr16:89816584-89816769 | Common:4; Rare:96; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89873533-89873888 | Common:4; Rare:151 | ||||
| chr16:89894658-89894982 | Common:5; Rare:78 | ||||
| chr16:89972478-89972669 | Common:1; Rare:71 |