| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22374542-22374892 | Common:1; Rare:128 | ||||
| chr16:22436923-22437055 | Rare:46 | ||||
| chr16:22437173-22437323 | Rare:46 | ||||
| chr16:22437563-22437594 | Common:2; Rare:8 | ||||
| chr16:22813924-22814181 | Common:2; Rare:48 | ||||
| chr16:22814758-22815040 | Common:2; Rare:95 | ||||
| chr16:23148659-23148855 | Common:1; Rare:53 | ||||
| chr16:23452952-23453021 | Rare:24 | ||||
| chr16:23453118-23453206 | Rare:29 | ||||
| chr16:23557287-23557755 | Common:3; Rare:173; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23561844-23561851 | Rare:1 | ||||
| chr16:23641099-23641546 | Common:3; Rare:146; Clinvar:12; Clinvar (benign):19; Clinvar (pathogenic):4 | ||||
| chr16:24540393-24540527 | Rare:34 | ||||
| chr16:24540532-24540891 | Common:1; Rare:93 | ||||
| chr16:24541034-24541078 | Common:1; Rare:12 |