| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89874029-89874446 | Common:5; Rare:117 | ||||
| chr16:89917826-89918135 | Common:3; Rare:92; Clinvar:5; Clinvar (benign):4 | ||||
| chr16:89918688-89918886 | Common:4; Rare:64; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:89921839-89921991 | Rare:34 | ||||
| chr16:89922962-89923067 | Common:1; Rare:27 | ||||
| chr16:89923084-89923397 | Common:1; Rare:129 | ||||
| chr16:89948070-89948209 | Rare:40 | ||||
| chr16:89948569-89948823 | Common:3; Rare:77 | ||||
| chr16:89972107-89972220 | Common:1; Rare:25 | ||||
| chr16:89972433-89972717 | Common:1; Rare:105 | ||||
| chr16:89972754-89973004 | Common:3; Rare:93 | ||||
| chr16:90019412-90019900 | Common:4; Rare:155 | ||||
| chr16:90019915-90020086 | Common:1; Rare:51 | ||||
| chr16:90020375-90020410 | Rare:5 | ||||
| chr16:90022252-90022356 | Rare:22 |