| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22436977-22437126 | Rare:52 | ||||
| chr16:22437158-22437302 | Rare:47 | ||||
| chr16:22437338-22437364 | Rare:4 | ||||
| chr16:23453127-23453250 | Rare:35 | ||||
| chr16:23557333-23557493 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641219-23641530 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678665-23678927 | Common:4; Rare:77 | ||||
| chr16:24255923-24256087 | Common:2; Rare:37 | ||||
| chr16:24539357-24539611 | Common:1; Rare:91 | ||||
| chr16:24729597-24729727 | Common:6; Rare:71 | ||||
| chr16:25015296-25015432 | Common:1; Rare:54 | ||||
| chr16:25111472-25111832 | Common:2; Rare:104 | ||||
| chr16:27268724-27268872 | Common:1; Rare:50 | ||||
| chr16:27549877-27550177 | Common:2; Rare:118 | ||||
| chr16:28491938-28492132 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 |