| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4847859-4848210 | Common:3; Rare:112 | ||||
| chr16:5033557-5033976 | Common:2; Rare:202; Clinvar:1 | ||||
| chr16:5071727-5071852 | Rare:56; Clinvar (benign):1 | ||||
| chr16:8621595-8621757 | Common:1; Rare:62 | ||||
| chr16:8797607-8797942 | Common:1; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868120-8868295 | Common:2; Rare:50 | ||||
| chr16:9091935-9092131 | Rare:75 | ||||
| chr16:10580581-10580709 | Rare:43 | ||||
| chr16:10743754-10743880 | Rare:49 | ||||
| chr16:10744069-10744279 | Common:1; Rare:77 | ||||
| chr16:10944674-10944761 | Rare:39 | ||||
| chr16:11024370-11024667 | Common:3; Rare:68 | ||||
| chr16:11256197-11256331 | Common:3; Rare:57 | ||||
| chr16:11345286-11345469 | Common:1; Rare:61 | ||||
| chr16:11586884-11587070 | Common:3; Rare:50 |