| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071791-5071861 | Rare:35; Clinvar (benign):1 | ||||
| chr16:5097728-5098015 | Common:4; Rare:102 | ||||
| chr16:6019442-6019580 | Common:1; Rare:46 | ||||
| chr16:6019763-6019901 | Rare:47; Clinvar:1 | ||||
| chr16:6483664-6483869 | Rare:71 | ||||
| chr16:7422623-7422790 | Common:3; Rare:50 | ||||
| chr16:8621601-8621707 | Common:1; Rare:44 | ||||
| chr16:8674372-8674654 | Common:1; Rare:100; Clinvar:2 | ||||
| chr16:8712727-8713224 | Common:5; Rare:122 | ||||
| chr16:8713233-8713337 | Common:2; Rare:12 | ||||
| chr16:8713869-8714026 | Rare:53 | ||||
| chr16:8797610-8797877 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868983-8869274 | Common:4; Rare:128 | ||||
| chr16:10385933-10386089 | Rare:58 | ||||
| chr16:10743725-10743912 | Rare:71 |