| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:83898870-83899203 | Common:10; Rare:355; Clinvar:3; Clinvar (benign):29 | ||||
| chr16:83899215-83900140 | Common:8; Rare:529; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr16:83953111-83953356 | Common:2; Rare:192 | ||||
| chr16:83953520-83953870 | Common:6; Rare:143 | ||||
| chr16:84116297-84116531 | Common:4; Rare:121 | ||||
| chr16:84116695-84117199 | Common:14; Rare:524 | ||||
| chr16:84144294-84144754 | Common:1; Rare:147 | ||||
| chr16:84144983-84145348 | Common:7; Rare:367; Clinvar:11 | ||||
| chr16:84175318-84175718 | Common:14; Rare:127 | ||||
| chr16:84175743-84176152 | Common:13; Rare:326; Clinvar:12; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr16:84368230-84368769 | Common:17; Rare:416 | ||||
| chr16:84406190-84406600 | Common:1; Rare:122 | ||||
| chr16:84407722-84408017 | Common:6; Rare:133 | ||||
| chr16:84408051-84408359 | Common:3; Rare:87 | ||||
| chr16:84504517-84504964 | Common:33; Rare:471 |