| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4847599-4847768 | Rare:65 | ||||
| chr16:4847822-4848007 | Common:2; Rare:63 | ||||
| chr16:4937107-4937473 | Common:5; Rare:116 | ||||
| chr16:4957737-4957840 | Common:2; Rare:33 | ||||
| chr16:4957891-4957949 | Rare:17 | ||||
| chr16:4957957-4958018 | Common:1; Rare:19 | ||||
| chr16:5033038-5033271 | Common:2; Rare:83 | ||||
| chr16:5033336-5033731 | Common:3; Rare:181; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:5033826-5034019 | Common:1; Rare:81 | ||||
| chr16:5071695-5072017 | Rare:164; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr16:5072019-5072343 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:5072355-5072520 | Common:2; Rare:38 | ||||
| chr16:5097299-5097579 | Common:6; Rare:98 | ||||
| chr16:5097681-5098173 | Common:4; Rare:164 | ||||
| chr16:8621552-8621811 | Common:1; Rare:97 |