| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400773-3400805 | Rare:9 | ||||
| chr16:3400841-3401363 | Common:8; Rare:181 | ||||
| chr16:3443428-3443766 | Common:4; Rare:123 | ||||
| chr16:3444020-3444068 | Rare:11 | ||||
| chr16:3444204-3444336 | Common:3; Rare:30 | ||||
| chr16:3457602-3457806 | Common:2; Rare:54 | ||||
| chr16:3457862-3458184 | Common:3; Rare:145 | ||||
| chr16:3500848-3501084 | Common:4; Rare:90 | ||||
| chr16:3501161-3501284 | Common:2; Rare:30 | ||||
| chr16:3611492-3611880 | Common:1; Rare:159; Clinvar:2 | ||||
| chr16:3642814-3642950 | Rare:36 | ||||
| chr16:3654656-3654893 | Common:2; Rare:71 | ||||
| chr16:3717284-3717865 | Common:1; Rare:220; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:3718031-3718172 | Rare:27 | ||||
| chr16:3879766-3880294 | Common:1; Rare:198 |