| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1361671-1361789 | Rare:53; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:1452766-1452995 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:1534817-1534834 | Rare:3 | ||||
| chr16:1536228-1536403 | Common:2; Rare:35 | ||||
| chr16:1729492-1729777 | Common:2; Rare:103 | ||||
| chr16:1827956-1828062 | Common:2; Rare:22 | ||||
| chr16:1828588-1828658 | Common:2; Rare:9 | ||||
| chr16:1878951-1879194 | Common:4; Rare:36 | ||||
| chr16:1965362-1965480 | Common:4; Rare:34 | ||||
| chr16:1978417-1978674 | Rare:119 | ||||
| chr16:2154816-2154876 | Common:1; Rare:19 | ||||
| chr16:2155098-2155152 | Rare:22 | ||||
| chr16:2170224-2170552 | Common:2; Rare:102 | ||||
| chr16:2175864-2176106 | Rare:77 | ||||
| chr16:2240407-2240510 | Common:1; Rare:27 |