| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20806426-20806533 | Rare:42 | ||||
| chr16:20900842-20900873 | Rare:8 | ||||
| chr16:21158664-21158720 | Rare:18 | ||||
| chr16:21953038-21953444 | Common:1; Rare:102; Clinvar (benign):3 | ||||
| chr16:22436942-22437063 | Rare:45 | ||||
| chr16:22437455-22437676 | Common:2; Rare:56 | ||||
| chr16:23557291-23557460 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23596130-23596462 | Common:2; Rare:101 | ||||
| chr16:23641153-23641530 | Common:3; Rare:117; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr16:23678714-23678967 | Common:4; Rare:79 | ||||
| chr16:24539312-24539618 | Common:2; Rare:103 | ||||
| chr16:24729598-24729844 | Common:7; Rare:104 | ||||
| chr16:25111472-25111859 | Common:2; Rare:114 | ||||
| chr16:27268719-27268872 | Common:1; Rare:52 | ||||
| chr16:27549838-27550167 | Common:2; Rare:125 |