| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4802615-4802696 | Rare:37; Clinvar:3 | ||||
| chr16:4802878-4802903 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:4802905-4802986 | Rare:40; Clinvar:2 | ||||
| chr16:4847231-4847436 | Common:1; Rare:89 | ||||
| chr16:4891850-4892181 | Common:5; Rare:162 | ||||
| chr16:5033922-5033967 | Rare:17 | ||||
| chr16:5071631-5071861 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr16:5097737-5098031 | Common:4; Rare:100 | ||||
| chr16:8797647-8797889 | Rare:92; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868995-8869274 | Common:4; Rare:121 | ||||
| chr16:11742827-11743006 | Common:1; Rare:68 | ||||
| chr16:11797196-11797520 | Common:2; Rare:121 | ||||
| chr16:11851517-11851653 | Rare:66 | ||||
| chr16:11897995-11898285 | Common:2; Rare:57 | ||||
| chr16:11915391-11915728 | Common:5; Rare:126 |