| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22437361-22437490 | Rare:43 | ||||
| chr16:22437505-22437695 | Common:2; Rare:49 | ||||
| chr16:23302148-23302398 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr16:23452489-23452801 | Rare:71 | ||||
| chr16:23452878-23453028 | Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:23453127-23453236 | Rare:31 | ||||
| chr16:23557327-23557460 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641219-23641545 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23706535-23706775 | Rare:37 | ||||
| chr16:23713169-23713318 | Rare:49 | ||||
| chr16:24539476-24539618 | Common:1; Rare:55 | ||||
| chr16:24729604-24729844 | Common:7; Rare:101 | ||||
| chr16:24730138-24730309 | Rare:59 | ||||
| chr16:25015248-25015461 | Common:2; Rare:70 | ||||
| chr16:25111521-25111852 | Common:2; Rare:104 |