| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31472321-31472494 | Rare:34 | ||||
| chr16:31472699-31472964 | Common:1; Rare:49 | ||||
| chr16:31507726-31507888 | Rare:52 | ||||
| chr16:31507954-31508125 | Common:1; Rare:56 | ||||
| chr16:31508293-31508570 | Common:4; Rare:119 | ||||
| chr16:31508663-31508733 | Common:1; Rare:19 | ||||
| chr16:31508900-31509057 | Rare:32 | ||||
| chr16:31713171-31713420 | Rare:60 | ||||
| chr16:31713522-31713700 | Common:1; Rare:43 | ||||
| chr16:31713779-31713863 | Rare:12 | ||||
| chr16:31873609-31873945 | Common:1; Rare:105 | ||||
| chr16:31874086-31874169 | Rare:13 | ||||
| chr16:46621293-46621511 | Common:1; Rare:86 | ||||
| chr16:46688602-46688808 | Rare:50 | ||||
| chr16:46688940-46689448 | Common:1; Rare:182; Clinvar:2; Clinvar (benign):1 |