| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88809636-88810036 | Common:2; Rare:168; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:88810293-88810727 | Common:3; Rare:318; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:88811287-88811928 | Common:10; Rare:465; Clinvar:3; Clinvar (benign):4 | ||||
| chr16:88811838-88812662 | Common:31; Rare:1069; Clinvar (benign):6 | ||||
| chr16:88856476-88856753 | Common:5; Rare:77 | ||||
| chr16:88856826-88857226 | Common:28; Rare:936; Clinvar:8; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr16:88976729-88977700 | Common:21; Rare:1113 | ||||
| chr16:89093660-89094230 | Common:35; Rare:659; Clinvar (benign):2 | ||||
| chr16:89098220-89098720 | Common:4; Rare:151; Clinvar (benign):3 | ||||
| chr16:89171250-89171759 | Common:13; Rare:165 | ||||
| chr16:89201615-89202001 | Common:10; Rare:465 | ||||
| chr16:89217369-89217769 | Common:10; Rare:671 | ||||
| chr16:89319924-89320324 | Common:5; Rare:166 | ||||
| chr16:89488969-89489785 | Common:41; Rare:804 | ||||
| chr16:89490268-89491182 | Common:43; Rare:1333 |