| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065532-30065827 | Rare:105 | ||||
| chr16:30075914-30076034 | Rare:41 | ||||
| chr16:30407475-30407622 | Rare:52 | ||||
| chr16:30534851-30535070 | Common:2; Rare:71 | ||||
| chr16:30762110-30762351 | Common:3; Rare:86 | ||||
| chr16:30923240-30923266 | Rare:12 | ||||
| chr16:31033460-31033576 | Rare:44 | ||||
| chr16:31459309-31459510 | Common:1; Rare:83 | ||||
| chr16:31471993-31472186 | Rare:47 | ||||
| chr16:31508365-31508484 | Common:2; Rare:49 | ||||
| chr16:46689141-46689387 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973603-46973757 | Rare:70 | ||||
| chr16:47461020-47461343 | Common:2; Rare:118; Clinvar (benign):1 | ||||
| chr16:50741974-50742179 | Common:1; Rare:78; Clinvar:1 | ||||
| chr16:53703818-53704179 | Rare:102; Clinvar:3; Clinvar (benign):1 |