| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3611558-3611784 | Rare:96; Clinvar:1 | ||||
| chr16:4425773-4425890 | Common:1; Rare:56 | ||||
| chr16:4476271-4476476 | Common:3; Rare:79 | ||||
| chr16:4734199-4734534 | Common:1; Rare:109 | ||||
| chr16:4767126-4767330 | Common:1; Rare:67 | ||||
| chr16:5033920-5033967 | Rare:19 | ||||
| chr16:8797610-8797877 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868973-8869228 | Common:4; Rare:116 | ||||
| chr16:10743742-10743882 | Rare:56 | ||||
| chr16:11742827-11743054 | Common:2; Rare:95 | ||||
| chr16:11851493-11851626 | Rare:70 | ||||
| chr16:11915889-11916254 | Common:2; Rare:147 | ||||
| chr16:11976604-11976766 | Common:3; Rare:66 | ||||
| chr16:14630161-14630413 | Rare:111 | ||||
| chr16:14632722-14632995 | Common:1; Rare:93 |