| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3716698-3717172 | Common:2; Rare:259 | ||||
| chr16:3717290-3717893 | Common:5; Rare:935; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:3879549-3880309 | Common:4; Rare:644 | ||||
| chr16:3880605-3881005 | Common:12; Rare:445 | ||||
| chr16:4116333-4116733 | Common:6; Rare:311 | ||||
| chr16:4263594-4263994 | Common:3; Rare:195 | ||||
| chr16:4272655-4273078 | Common:5; Rare:303 | ||||
| chr16:4273074-4273809 | Common:6; Rare:393 | ||||
| chr16:4350682-4351159 | Common:8; Rare:186 | ||||
| chr16:4351211-4351617 | Common:12; Rare:699 | ||||
| chr16:4371317-4371981 | Common:6; Rare:799 | ||||
| chr16:4415458-4416597 | Common:10; Rare:770 | ||||
| chr16:4416524-4416924 | Common:1; Rare:239 | ||||
| chr16:4424728-4425128 | Common:1; Rare:91 | ||||
| chr16:4425388-4426838 | Common:28; Rare:1540 |