| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84711565-84711711 | Rare:40 | ||||
| chr16:84720915-84721167 | Common:5; Rare:78 | ||||
| chr16:84730540-84730654 | Common:3; Rare:31 | ||||
| chr16:85171820-85171939 | Common:2; Rare:26 | ||||
| chr16:85173635-85173885 | Common:2; Rare:64 | ||||
| chr16:85245193-85245424 | Common:4; Rare:53 | ||||
| chr16:85477649-85477863 | Common:2; Rare:61 | ||||
| chr16:85575925-85576210 | Common:2; Rare:42 | ||||
| chr16:85748682-85748917 | Rare:42 | ||||
| chr16:85776513-85776604 | Rare:20 | ||||
| chr16:85807319-85807584 | Common:2; Rare:64 | ||||
| chr16:85844257-85844514 | Common:9; Rare:41 | ||||
| chr16:86387505-86387727 | Common:2; Rare:66 | ||||
| chr16:86565184-86565270 | Common:3; Rare:20 | ||||
| chr16:86567752-86567975 | Common:1; Rare:91; Clinvar (benign):1 |