| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3161320-3161790 | Common:3; Rare:93 | ||||
| chr16:3168640-3169070 | Common:3; Rare:142 | ||||
| chr16:3174083-3174552 | Common:1; Rare:145 | ||||
| chr16:3175560-3175850 | Common:6; Rare:193 | ||||
| chr16:3182710-3183055 | Common:5; Rare:117 | ||||
| chr16:3183210-3183729 | Common:8; Rare:235 | ||||
| chr16:3189389-3189753 | Common:3; Rare:152 | ||||
| chr16:3191383-3191806 | Common:4; Rare:150 | ||||
| chr16:3264300-3264791 | Common:6; Rare:436 | ||||
| chr16:3274556-3274899 | Rare:108 | ||||
| chr16:3375339-3375989 | Common:9; Rare:167 | ||||
| chr16:3646090-3646640 | Common:1; Rare:149 | ||||
| chr16:3650101-3651002 | Common:12; Rare:266 | ||||
| chr16:3665909-3666351 | Common:2; Rare:256; Clinvar:1 | ||||
| chr16:3679428-3679897 | Common:4; Rare:383; Clinvar:3; Clinvar (benign):3 |