| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2474904-2475156 | Rare:80; Clinvar (benign):2 | ||||
| chr16:2513645-2514035 | Rare:143 | ||||
| chr16:2518989-2519391 | Rare:101 | ||||
| chr16:2777235-2777380 | Common:1; Rare:58 | ||||
| chr16:2911748-2912018 | Common:3; Rare:91 | ||||
| chr16:3065136-3065462 | Common:4; Rare:97 | ||||
| chr16:3112500-3112605 | Rare:25 | ||||
| chr16:3134861-3135151 | Common:3; Rare:80 | ||||
| chr16:3305397-3305518 | Common:1; Rare:42 | ||||
| chr16:3305725-3305835 | Rare:35 | ||||
| chr16:3400971-3401197 | Common:4; Rare:86 | ||||
| chr16:3443450-3443757 | Common:3; Rare:110 | ||||
| chr16:3457914-3458131 | Common:2; Rare:106 | ||||
| chr16:4476317-4476481 | Rare:64 | ||||
| chr16:4538394-4538619 | Common:3; Rare:75 |