| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89720865-89720970 | Common:1; Rare:29 | ||||
| chr16:89816617-89816758 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873442-89873658 | Common:4; Rare:105 | ||||
| chr16:89923171-89923345 | Rare:63 | ||||
| chr16:89972462-89972648 | Common:1; Rare:68 | ||||
| chr16:90019420-90019681 | Common:4; Rare:83 | ||||
| chr16:90022532-90022715 | Rare:73 | ||||
| chr17:331023-331176 | Common:6; Rare:34 | ||||
| chr17:386209-386286 | Common:2; Rare:17 | ||||
| chr17:409989-410373 | Common:8; Rare:164 | ||||
| chr17:714776-714953 | Common:3; Rare:58 | ||||
| chr17:752146-752333 | Common:2; Rare:74 | ||||
| chr17:752766-752902 | Rare:31 | ||||
| chr17:996781-997175 | Common:2; Rare:125 | ||||
| chr17:1031809-1032061 | Common:4; Rare:60 |