| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88569895-88569932 | Rare:9 | ||||
| chr16:88570084-88570495 | Common:2; Rare:156 | ||||
| chr16:88650034-88650265 | Common:1; Rare:51 | ||||
| chr16:88650357-88650524 | Common:1; Rare:66 | ||||
| chr16:88650577-88650687 | Common:1; Rare:33 | ||||
| chr16:88650974-88651235 | Common:1; Rare:89; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88651452-88651746 | Common:4; Rare:70 | ||||
| chr16:88662975-88663432 | Common:11; Rare:209 | ||||
| chr16:88686487-88686816 | Common:3; Rare:103 | ||||
| chr16:88700922-88701268 | Common:2; Rare:117 | ||||
| chr16:88703532-88703825 | Common:4; Rare:96 | ||||
| chr16:88706293-88706608 | Common:5; Rare:155 | ||||
| chr16:88785146-88785369 | Common:2; Rare:85 | ||||
| chr16:88785600-88785741 | Rare:29 | ||||
| chr16:88802597-88802889 | Common:5; Rare:64 |