| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4668494-4668650 | Common:6; Rare:93 | ||||
| chr16:4679781-4680181 | Common:4; Rare:259 | ||||
| chr16:4693324-4693817 | Common:11; Rare:530 | ||||
| chr16:4734057-4734626 | Common:4; Rare:533 | ||||
| chr16:4767045-4767452 | Common:6; Rare:293 | ||||
| chr16:4794900-4796616 | Common:21; Rare:1009 | ||||
| chr16:4802548-4803191 | Common:7; Rare:651; Clinvar:24; Clinvar (benign):3 | ||||
| chr16:4847191-4847764 | Common:10; Rare:610 | ||||
| chr16:4937028-4937487 | Common:17; Rare:384 | ||||
| chr16:4957910-4958423 | Common:17; Rare:246 | ||||
| chr16:5033430-5034120 | Common:7; Rare:564; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:5071721-5071941 | Rare:286; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr16:5072046-5072480 | Common:9; Rare:181; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:5097669-5098310 | Common:12; Rare:415 | ||||
| chr16:8621555-8621800 | Common:3; Rare:216 |