| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689518-46689728 | Common:2; Rare:92; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973638-46973733 | Rare:49 | ||||
| chr16:47461043-47461345 | Common:2; Rare:105; Clinvar (benign):2 | ||||
| chr16:48385295-48385534 | Common:3; Rare:94 | ||||
| chr16:50245935-50246174 | Common:2; Rare:55 | ||||
| chr16:53054916-53055048 | Common:1; Rare:26 | ||||
| chr16:53703825-53704216 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:55508804-55509129 | Common:1; Rare:83 | ||||
| chr16:56451135-56451763 | Common:5; Rare:206 | ||||
| chr16:56625646-56625826 | Rare:51 | ||||
| chr16:56729958-56730195 | Common:1; Rare:58 | ||||
| chr16:56931923-56932177 | Common:2; Rare:130 | ||||
| chr16:56989384-56989602 | Common:1; Rare:52; Clinvar:1 | ||||
| chr16:57185984-57186371 | Common:1; Rare:118 | ||||
| chr16:57447349-57447517 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 |