| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22297364-22297532 | Common:1; Rare:64 | ||||
| chr16:22374575-22374796 | Common:1; Rare:77 | ||||
| chr16:22436918-22437058 | Rare:50 | ||||
| chr16:22437449-22437583 | Rare:41 | ||||
| chr16:23452725-23452785 | Rare:18 | ||||
| chr16:23453127-23453241 | Rare:32 | ||||
| chr16:23510445-23510723 | Common:4; Rare:104 | ||||
| chr16:23557207-23557567 | Common:2; Rare:136; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:23641121-23641557 | Common:3; Rare:141; Clinvar:9; Clinvar (benign):16; Clinvar (pathogenic):3 | ||||
| chr16:23678812-23679127 | Common:4; Rare:104 | ||||
| chr16:24539425-24539682 | Common:1; Rare:106 | ||||
| chr16:24540896-24541078 | Common:1; Rare:41 | ||||
| chr16:24729500-24730284 | Common:10; Rare:277 | ||||
| chr16:25015282-25015514 | Common:2; Rare:76 | ||||
| chr16:25111508-25111792 | Common:2; Rare:76 |