| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53562-53870 | Common:6; Rare:105 | ||||
| chr16:636250-636427 | Common:4; Rare:58 | ||||
| chr16:649243-649346 | Rare:36 | ||||
| chr16:740986-741160 | Rare:53 | ||||
| chr16:2047813-2048050 | Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268078-2268186 | Common:1; Rare:47 | ||||
| chr16:2777238-2777371 | Common:1; Rare:50 | ||||
| chr16:3112491-3112608 | Common:1; Rare:30 | ||||
| chr16:3134861-3135136 | Common:3; Rare:71 | ||||
| chr16:3305428-3305494 | Common:1; Rare:18 | ||||
| chr16:3400967-3401197 | Common:4; Rare:88 | ||||
| chr16:3611594-3611783 | Rare:80 | ||||
| chr16:4425767-4425907 | Common:1; Rare:74 | ||||
| chr16:4693476-4693729 | Common:2; Rare:110 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 |