| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8674337-8674890 | Common:4; Rare:375; Clinvar:8 | ||||
| chr16:8797521-8797956 | Common:7; Rare:441; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):10 | ||||
| chr16:8861106-8861743 | Common:10; Rare:238 | ||||
| chr16:8867465-8868570 | Common:11; Rare:634 | ||||
| chr16:8868619-8869341 | Common:17; Rare:653 | ||||
| chr16:8962990-8963720 | Common:10; Rare:372 | ||||
| chr16:8963768-8964159 | Common:5; Rare:311 | ||||
| chr16:8964260-8964580 | Rare:98 | ||||
| chr16:9091131-9091243 | Rare:44 | ||||
| chr16:9091156-9091766 | Common:6; Rare:534 | ||||
| chr16:9091769-9091968 | Rare:126 | ||||
| chr16:9092507-9093077 | Common:16; Rare:455 | ||||
| chr16:10385836-10386350 | Common:3; Rare:312 | ||||
| chr16:10580113-10580370 | Common:3; Rare:182 | ||||
| chr16:10580517-10580901 | Common:4; Rare:307 |