| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23452621-23452815 | Rare:61; Clinvar (benign):1 | ||||
| chr16:23453127-23453211 | Rare:27 | ||||
| chr16:23557327-23557557 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641220-23641543 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539326-24539630 | Common:2; Rare:104 | ||||
| chr16:24540304-24540483 | Rare:49 | ||||
| chr16:24729611-24729844 | Common:7; Rare:99 | ||||
| chr16:25015265-25015457 | Common:2; Rare:67 | ||||
| chr16:25111472-25111855 | Common:2; Rare:112 | ||||
| chr16:27268719-27268873 | Common:1; Rare:53 | ||||
| chr16:27313804-27313997 | Common:2; Rare:52 | ||||
| chr16:27549838-27550167 | Common:2; Rare:125 | ||||
| chr16:28491913-28492138 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494297-28494684 | Common:1; Rare:80 | ||||
| chr16:28506832-28507027 | Rare:44 |