| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1983812-1984309 | Common:16; Rare:369; Clinvar (benign):11 | ||||
| chr16:1989742-1990039 | Common:2; Rare:93 | ||||
| chr16:1989989-1990584 | Common:7; Rare:305 | ||||
| chr16:1992140-1992500 | Common:6; Rare:161 | ||||
| chr16:2009574-2010059 | Common:49; Rare:452 | ||||
| chr16:2010263-2010426 | Common:1; Rare:47 | ||||
| chr16:2026759-2027204 | Common:8; Rare:318 | ||||
| chr16:2046862-2047392 | Common:5; Rare:181 | ||||
| chr16:2047704-2048078 | Rare:497; Clinvar:6; Clinvar (benign):17; Clinvar (pathogenic):2 | ||||
| chr16:2048207-2048817 | Rare:253; Clinvar:9; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr16:2135701-2136377 | Common:10; Rare:781; Clinvar (benign):3 | ||||
| chr16:2148021-2148294 | Common:2; Rare:101 | ||||
| chr16:2148457-2148744 | Rare:155 | ||||
| chr16:2148775-2149280 | Common:2; Rare:179 | ||||
| chr16:2155209-2155891 | Common:4; Rare:569 |