| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75555180-75555410 | Common:2; Rare:52 | ||||
| chr16:75556207-75556420 | Common:2; Rare:79; Clinvar (benign):4 | ||||
| chr16:75566239-75566425 | Common:1; Rare:99 | ||||
| chr16:75623222-75623433 | Common:3; Rare:77 | ||||
| chr16:75647590-75647896 | Common:8; Rare:288; Clinvar:8; Clinvar (pathogenic):2 | ||||
| chr16:77190674-77191025 | Common:24; Rare:227 | ||||
| chr16:77191133-77191241 | Common:1; Rare:45 | ||||
| chr16:77722280-77722611 | Common:8; Rare:209 | ||||
| chr16:78099512-78099888 | Common:4; Rare:280; Clinvar:4; Clinvar (benign):13 | ||||
| chr16:81006360-81006562 | Common:1; Rare:87 | ||||
| chr16:81006782-81007288 | Common:8; Rare:325 | ||||
| chr16:81007305-81007767 | Common:17; Rare:271 | ||||
| chr16:81077060-81077400 | Common:4; Rare:290 | ||||
| chr16:81314771-81315034 | Common:4; Rare:238; Clinvar:4 | ||||
| chr16:81444489-81445347 | Common:5; Rare:478 |