| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1078540-1078950 | Common:1; Rare:151 | ||||
| chr16:1308866-1309187 | Common:5; Rare:165 | ||||
| chr16:1309367-1309730 | Rare:253 | ||||
| chr16:1351785-1352017 | Common:4; Rare:226; Clinvar:12; Clinvar (benign):2 | ||||
| chr16:1379562-1379784 | Common:2; Rare:91 | ||||
| chr16:1414632-1414927 | Common:7; Rare:160 | ||||
| chr16:1420687-1420954 | Common:2; Rare:216 | ||||
| chr16:1474822-1475182 | Common:10; Rare:251; Clinvar:10; Clinvar (benign):4 | ||||
| chr16:1493228-1493614 | Common:8; Rare:213 | ||||
| chr16:1610332-1610435 | Rare:25 | ||||
| chr16:1611966-1612452 | Common:8; Rare:355; Clinvar:4 | ||||
| chr16:1678110-1678351 | Common:6; Rare:159 | ||||
| chr16:1706026-1706464 | Common:7; Rare:215; Clinvar (pathogenic):1 | ||||
| chr16:1771521-1771970 | Common:7; Rare:242 | ||||
| chr16:1773047-1773271 | Common:2; Rare:147; Clinvar (pathogenic):2 |