| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3020850-3021310 | Rare:133 | ||||
| chr16:3024140-3024530 | Common:6; Rare:257 | ||||
| chr16:3065207-3065423 | Common:6; Rare:110 | ||||
| chr16:3112436-3112628 | Common:4; Rare:82 | ||||
| chr16:3134790-3135209 | Common:6; Rare:217 | ||||
| chr16:3256619-3256750 | Rare:26 | ||||
| chr16:3263672-3263862 | Common:2; Rare:84 | ||||
| chr16:3282700-3283110 | Common:6; Rare:205 | ||||
| chr16:3283222-3283558 | Common:9; Rare:176 | ||||
| chr16:3305394-3305526 | Common:2; Rare:72 | ||||
| chr16:3400929-3401294 | Common:12; Rare:268 | ||||
| chr16:3443449-3443737 | Common:6; Rare:187 | ||||
| chr16:3457879-3458135 | Common:6; Rare:238 | ||||
| chr16:3611552-3611843 | Common:2; Rare:224; Clinvar:1 | ||||
| chr16:3717418-3717680 | Common:2; Rare:216; Clinvar:2; Clinvar (benign):2 |