| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30609464-30609930 | Rare:276 | ||||
| chr16:30609970-30610190 | Common:1; Rare:84 | ||||
| chr16:30610204-30610599 | Common:3; Rare:271 | ||||
| chr16:30650163-30651042 | Common:1; Rare:426 | ||||
| chr16:30650958-30651065 | Rare:34 | ||||
| chr16:30651320-30651680 | Rare:227 | ||||
| chr16:30657800-30658086 | Common:2; Rare:97 | ||||
| chr16:30658021-30659485 | Common:5; Rare:1031 | ||||
| chr16:30659831-30660208 | Rare:265 | ||||
| chr16:30697995-30698814 | Common:5; Rare:734 | ||||
| chr16:30698923-30699425 | Rare:388; Clinvar (benign):3 | ||||
| chr16:30748044-30748564 | Common:7; Rare:328; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30761380-30761637 | Rare:234 | ||||
| chr16:30761984-30762387 | Common:10; Rare:343 | ||||
| chr16:30762390-30763109 | Common:4; Rare:253 |