| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:690389-690414 | Common:1; Rare:11 | ||||
| chr16:740968-741150 | Rare:57 | ||||
| chr16:1420707-1420937 | Common:1; Rare:95 | ||||
| chr16:1533437-1533744 | Common:2; Rare:65 | ||||
| chr16:1772612-1772905 | Common:3; Rare:96; Clinvar (pathogenic):2 | ||||
| chr16:1782510-1782903 | Common:4; Rare:127 | ||||
| chr16:1827192-1827298 | Rare:62 | ||||
| chr16:1943133-1943491 | Common:1; Rare:114 | ||||
| chr16:1964814-1964992 | Common:6; Rare:80 | ||||
| chr16:1971800-1972110 | Common:3; Rare:91 | ||||
| chr16:2047784-2048050 | Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205697-2205885 | Common:4; Rare:89 | ||||
| chr16:2268063-2268187 | Common:1; Rare:61 | ||||
| chr16:2429125-2429478 | Common:2; Rare:116 | ||||
| chr16:2459940-2460147 | Common:1; Rare:61 |