| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1421080-1421310 | Common:17; Rare:115 | ||||
| chr16:1474099-1474499 | Common:5; Rare:168 | ||||
| chr16:1474838-1475243 | Common:16; Rare:325; Clinvar:7; Clinvar (benign):4 | ||||
| chr16:1492850-1493643 | Common:15; Rare:480 | ||||
| chr16:1610200-1610506 | Common:3; Rare:179 | ||||
| chr16:1610540-1611156 | Common:3; Rare:438; Clinvar:3 | ||||
| chr16:1611857-1612535 | Common:15; Rare:649; Clinvar:6 | ||||
| chr16:1612623-1613023 | Common:5; Rare:255 | ||||
| chr16:1613960-1614352 | Common:4; Rare:121 | ||||
| chr16:1614363-1614763 | Rare:135 | ||||
| chr16:1677917-1678562 | Common:11; Rare:521 | ||||
| chr16:1679908-1681111 | Common:4; Rare:470 | ||||
| chr16:1705560-1705940 | Common:6; Rare:153 | ||||
| chr16:1705906-1706460 | Common:11; Rare:366; Clinvar (pathogenic):1 | ||||
| chr16:1706563-1706963 | Rare:137 |