| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1984388-1984492 | Rare:33; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr16:1984495-1984779 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr16:1989929-1989985 | Rare:11 | ||||
| chr16:1990302-1990431 | Common:1; Rare:24 | ||||
| chr16:2009694-2010061 | Common:16; Rare:143 | ||||
| chr16:2010272-2010443 | Common:1; Rare:47 | ||||
| chr16:2026750-2026911 | Common:1; Rare:58 | ||||
| chr16:2035760-2035946 | Common:2; Rare:72 | ||||
| chr16:2047737-2048056 | Rare:160; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:2091151-2091625 | Common:19; Rare:217; Clinvar:3; Clinvar (benign):7 | ||||
| chr16:2091781-2091808 | Rare:12; Clinvar (benign):1 | ||||
| chr16:2092419-2092534 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr16:2135289-2135573 | Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:2135867-2136188 | Common:1; Rare:154; Clinvar (benign):1 | ||||
| chr16:2155253-2155861 | Common:2; Rare:209 |