| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89701637-89701839 | Common:1; Rare:76 | ||||
| chr16:89702035-89702240 | Common:7; Rare:62 | ||||
| chr16:89720678-89721049 | Common:1; Rare:123 | ||||
| chr16:89816613-89816769 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873482-89873845 | Common:3; Rare:164 | ||||
| chr16:89873856-89874047 | Common:4; Rare:53 | ||||
| chr16:89923117-89923450 | Rare:132 | ||||
| chr16:89948560-89948806 | Common:3; Rare:74 | ||||
| chr16:89972468-89972894 | Common:3; Rare:158 | ||||
| chr16:90019420-90019675 | Common:4; Rare:81 | ||||
| chr16:90022520-90022703 | Rare:71 | ||||
| chr17:409986-410425 | Common:9; Rare:198 | ||||
| chr17:714770-714953 | Common:3; Rare:60 | ||||
| chr17:732239-732607 | Common:1; Rare:124 | ||||
| chr17:752146-752360 | Common:2; Rare:84 |