| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70114124-70114376 | Common:3; Rare:91 | ||||
| chr16:70251941-70252132 | Common:1; Rare:60 | ||||
| chr16:70299132-70299205 | Rare:12 | ||||
| chr16:70346759-70346959 | Common:1; Rare:98 | ||||
| chr16:70523533-70523844 | Common:3; Rare:100; Clinvar (pathogenic):1 | ||||
| chr16:71808778-71808796 | Rare:9 | ||||
| chr16:72093572-72093934 | Rare:90 | ||||
| chr16:74296719-74296882 | Rare:63 | ||||
| chr16:75433288-75433787 | Common:4; Rare:169 | ||||
| chr16:75556205-75556416 | Common:2; Rare:80; Clinvar (benign):4 | ||||
| chr16:75566183-75566434 | Common:2; Rare:112 | ||||
| chr16:75647601-75647794 | Common:1; Rare:96; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:79600715-79600892 | Common:1; Rare:50 | ||||
| chr16:81006832-81007263 | Common:3; Rare:142 | ||||
| chr16:84116742-84117072 | Common:4; Rare:135 |