| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2756878-2757074 | Rare:54 | ||||
| chr16:2758492-2758762 | Common:1; Rare:75 | ||||
| chr16:2777231-2777389 | Common:1; Rare:64 | ||||
| chr16:2964041-2964295 | Common:2; Rare:63 | ||||
| chr16:2980372-2980672 | Common:2; Rare:100 | ||||
| chr16:3020437-3020496 | Rare:13 | ||||
| chr16:3023662-3024367 | Common:2; Rare:231 | ||||
| chr16:3134841-3135062 | Common:2; Rare:53 | ||||
| chr16:3283265-3283574 | Common:4; Rare:91 | ||||
| chr16:3305419-3305554 | Common:1; Rare:50 | ||||
| chr16:3305723-3305770 | Rare:14 | ||||
| chr16:3400962-3401268 | Common:6; Rare:116 | ||||
| chr16:3443450-3443734 | Common:3; Rare:96 | ||||
| chr16:3611551-3611807 | Rare:107; Clinvar:1 | ||||
| chr16:3717423-3717630 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):1 |