| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89720642-89721004 | Common:2; Rare:117 | ||||
| chr16:89816613-89816734 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873482-89873855 | Common:3; Rare:168 | ||||
| chr16:89923167-89923452 | Rare:113 | ||||
| chr16:89972435-89972597 | Common:1; Rare:57 | ||||
| chr16:90019415-90019664 | Common:4; Rare:77 | ||||
| chr16:90019740-90019909 | Rare:57 | ||||
| chr16:90022594-90022709 | Rare:47 | ||||
| chr16:90029169-90029301 | Common:9; Rare:79 | ||||
| chr17:714770-714962 | Common:3; Rare:61 | ||||
| chr17:732338-733150 | Common:10; Rare:305 | ||||
| chr17:751533-751640 | Rare:23 | ||||
| chr17:752149-752360 | Common:2; Rare:83 | ||||
| chr17:979412-979508 | Common:1; Rare:32 | ||||
| chr17:979689-979965 | Common:3; Rare:132 |