| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4538752-4538899 | Rare:59 | ||||
| chr16:4614871-4615080 | Common:1; Rare:62 | ||||
| chr16:4616227-4616524 | Rare:78 | ||||
| chr16:4693494-4693721 | Common:2; Rare:97 | ||||
| chr16:4734199-4734534 | Common:1; Rare:109 | ||||
| chr16:4767126-4767330 | Common:1; Rare:67 | ||||
| chr16:4847239-4847445 | Common:1; Rare:89 | ||||
| chr16:5033926-5033992 | Rare:24 | ||||
| chr16:5071781-5071860 | Rare:37; Clinvar (benign):1 | ||||
| chr16:8797610-8797885 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868977-8869291 | Common:5; Rare:139 | ||||
| chr16:10580569-10580748 | Rare:55 | ||||
| chr16:10743718-10743880 | Rare:71 | ||||
| chr16:10744056-10744301 | Common:1; Rare:91 | ||||
| chr16:10878785-10878940 | Rare:32 |