| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69762266-69762379 | Common:1; Rare:28 | ||||
| chr16:70114117-70114393 | Common:3; Rare:99 | ||||
| chr16:70289440-70289664 | Rare:80; Clinvar:1 | ||||
| chr16:70299072-70299205 | Common:1; Rare:23 | ||||
| chr16:70346804-70346959 | Common:1; Rare:79 | ||||
| chr16:70523533-70523852 | Common:3; Rare:104; Clinvar (pathogenic):1 | ||||
| chr16:71289245-71289696 | Common:5; Rare:139 | ||||
| chr16:71564911-71565015 | Common:1; Rare:38 | ||||
| chr16:71808774-71809339 | Common:4; Rare:207 | ||||
| chr16:71845905-71846023 | Common:1; Rare:37 | ||||
| chr16:71895254-71895582 | Common:3; Rare:125 | ||||
| chr16:72093508-72093934 | Rare:108 | ||||
| chr16:74296723-74296882 | Rare:61 | ||||
| chr16:74666857-74667082 | Common:1; Rare:77 | ||||
| chr16:75433339-75433792 | Common:4; Rare:149 |