| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4802918-4803111 | Common:3; Rare:91 | ||||
| chr16:4846634-4846706 | Common:1; Rare:18 | ||||
| chr16:4847199-4847785 | Common:3; Rare:255 | ||||
| chr16:5033569-5033992 | Common:2; Rare:204 | ||||
| chr16:5071717-5071959 | Rare:129; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072027-5072192 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:5072199-5072306 | Rare:24 | ||||
| chr16:5097669-5097981 | Common:4; Rare:129 | ||||
| chr16:8621313-8621395 | Common:2; Rare:22 | ||||
| chr16:8621585-8621778 | Common:1; Rare:78 | ||||
| chr16:8674389-8674696 | Common:1; Rare:106; Clinvar:2 | ||||
| chr16:8797505-8797912 | Common:3; Rare:167; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:8798068-8798081 | Rare:3 | ||||
| chr16:8868246-8868468 | Common:1; Rare:56 | ||||
| chr16:8868671-8868853 | Rare:49 |