| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4476336-4476473 | Rare:55 | ||||
| chr16:4538427-4538619 | Common:2; Rare:70 | ||||
| chr16:4614877-4615047 | Common:1; Rare:46 | ||||
| chr16:4693434-4693735 | Common:2; Rare:133 | ||||
| chr16:4734179-4734534 | Common:1; Rare:117 | ||||
| chr16:4767129-4767349 | Common:1; Rare:74 | ||||
| chr16:4802878-4803082 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4847226-4847445 | Common:1; Rare:94 | ||||
| chr16:5071778-5071852 | Rare:35; Clinvar (benign):1 | ||||
| chr16:5097719-5098030 | Common:4; Rare:112 | ||||
| chr16:8797621-8797885 | Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:10580569-10580853 | Common:2; Rare:96 | ||||
| chr16:11586891-11587023 | Common:1; Rare:39 | ||||
| chr16:11742858-11743054 | Common:2; Rare:80 | ||||
| chr16:11797176-11797483 | Common:2; Rare:115 |