| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734125-4734550 | Common:1; Rare:240 | ||||
| chr16:4767114-4767352 | Common:3; Rare:143 | ||||
| chr16:4802619-4802798 | Rare:59; Clinvar:5 | ||||
| chr16:4802858-4803082 | Common:2; Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4847223-4847734 | Common:6; Rare:361 | ||||
| chr16:4847890-4848220 | Common:3; Rare:168 | ||||
| chr16:4937112-4937368 | Common:9; Rare:141 | ||||
| chr16:5033602-5034008 | Common:2; Rare:235 | ||||
| chr16:5071775-5071938 | Rare:179; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr16:5097601-5098151 | Common:8; Rare:299 | ||||
| chr16:8621589-8621757 | Common:1; Rare:63 | ||||
| chr16:8797599-8797947 | Common:2; Rare:256; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr16:8868972-8869306 | Common:12; Rare:294 | ||||
| chr16:8963864-8964228 | Common:7; Rare:206 | ||||
| chr16:9091546-9091699 | Common:1; Rare:74 |