| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132547-69132663 | Rare:47 | ||||
| chr16:69726554-69726806 | Common:3; Rare:56 | ||||
| chr16:69762288-69762385 | Rare:22 | ||||
| chr16:70346759-70346937 | Common:1; Rare:86 | ||||
| chr16:70523532-70523844 | Common:3; Rare:100; Clinvar (pathogenic):1 | ||||
| chr16:71808774-71809126 | Common:1; Rare:149 | ||||
| chr16:71845890-71846017 | Common:2; Rare:41 | ||||
| chr16:71895254-71895588 | Common:3; Rare:127 | ||||
| chr16:72093602-72093934 | Rare:77 | ||||
| chr16:74296722-74296902 | Rare:76 | ||||
| chr16:75433416-75433797 | Common:4; Rare:117 | ||||
| chr16:75623232-75623427 | Common:3; Rare:69 | ||||
| chr16:75647638-75647799 | Common:1; Rare:78; Clinvar:3 | ||||
| chr16:77190725-77191002 | Common:10; Rare:92 | ||||
| chr16:79600732-79600947 | Common:1; Rare:62 |