| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734814-4735018 | Common:1; Rare:120 | ||||
| chr16:4766235-4766673 | Common:7; Rare:331 | ||||
| chr16:4767065-4767465 | Common:12; Rare:535 | ||||
| chr16:4788603-4789126 | Common:4; Rare:244 | ||||
| chr16:4800289-4800689 | Common:1; Rare:204; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr16:4801813-4802420 | Common:3; Rare:632; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:4802524-4803274 | Common:16; Rare:1177; Clinvar:41; Clinvar (benign):4 | ||||
| chr16:4846208-4846703 | Common:6; Rare:184 | ||||
| chr16:4847202-4848615 | Common:32; Rare:1532 | ||||
| chr16:4937120-4937490 | Common:5; Rare:121 | ||||
| chr16:4957714-4958382 | Common:37; Rare:541 | ||||
| chr16:5033410-5034015 | Common:10; Rare:843; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:5071601-5072001 | Common:1; Rare:475; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):5 | ||||
| chr16:5072060-5072485 | Common:9; Rare:249; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:5097671-5098071 | Common:20; Rare:480 |