| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4624651-4624879 | Common:1; Rare:90 | ||||
| chr16:4693482-4693726 | Common:2; Rare:106 | ||||
| chr16:4734185-4734534 | Common:1; Rare:116 | ||||
| chr16:4767120-4767321 | Common:2; Rare:67 | ||||
| chr16:5033920-5033985 | Rare:27 | ||||
| chr16:5071764-5071861 | Rare:44; Clinvar (benign):1 | ||||
| chr16:5097726-5098007 | Common:4; Rare:104 | ||||
| chr16:8797595-8797895 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868982-8869274 | Common:4; Rare:128 | ||||
| chr16:9091565-9091649 | Rare:39 | ||||
| chr16:10385933-10386077 | Rare:54 | ||||
| chr16:10580566-10580756 | Rare:58 | ||||
| chr16:10743740-10743869 | Rare:48 | ||||
| chr16:10744061-10744308 | Common:1; Rare:92 | ||||
| chr16:10944318-10944638 | Common:1; Rare:101 |