| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70523539-70523861 | Common:3; Rare:102 | ||||
| chr16:71808774-71809354 | Common:4; Rare:213 | ||||
| chr16:71895348-71895574 | Rare:77 | ||||
| chr16:72093602-72093934 | Rare:77 | ||||
| chr16:74296722-74296876 | Rare:59 | ||||
| chr16:75433416-75433784 | Common:4; Rare:110 | ||||
| chr16:75464388-75464448 | Common:2; Rare:26 | ||||
| chr16:75555274-75555417 | Common:1; Rare:33 | ||||
| chr16:75566179-75566431 | Common:2; Rare:112 | ||||
| chr16:75623232-75623427 | Common:3; Rare:69 | ||||
| chr16:75647584-75647822 | Common:2; Rare:115; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190707-77191004 | Common:10; Rare:97 | ||||
| chr16:77191086-77191231 | Common:2; Rare:59 | ||||
| chr16:77722281-77722547 | Common:4; Rare:80 | ||||
| chr16:78099515-78099759 | Common:1; Rare:109; Clinvar (benign):4 |