| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30021261-30021507 | Rare:47 | ||||
| chr16:30021610-30021789 | Rare:31 | ||||
| chr16:30052890-30053211 | Common:1; Rare:99; Clinvar (benign):1 | ||||
| chr16:30053630-30053944 | Common:1; Rare:52 | ||||
| chr16:30064107-30064193 | Rare:21 | ||||
| chr16:30065033-30065902 | Rare:261 | ||||
| chr16:30066034-30066140 | Rare:32 | ||||
| chr16:30066495-30066799 | Rare:75 | ||||
| chr16:30075833-30076159 | Common:1; Rare:99 | ||||
| chr16:30091895-30092170 | Common:1; Rare:64 | ||||
| chr16:30096199-30096487 | Common:1; Rare:81 | ||||
| chr16:30122938-30123077 | Common:1; Rare:38 | ||||
| chr16:30123194-30123432 | Common:5; Rare:67 | ||||
| chr16:30123467-30123627 | Rare:26 | ||||
| chr16:30183458-30183617 | Common:1; Rare:41 |