| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88705716-88706011 | Common:1; Rare:89 | ||||
| chr16:88706329-88706649 | Common:5; Rare:157 | ||||
| chr16:88784595-88784838 | Common:1; Rare:59 | ||||
| chr16:88784901-88785021 | Common:1; Rare:47 | ||||
| chr16:88785135-88785319 | Common:2; Rare:71 | ||||
| chr16:88785547-88785701 | Rare:34 | ||||
| chr16:88803437-88803864 | Common:6; Rare:180 | ||||
| chr16:88804466-88804725 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr16:88810420-88810731 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:88811368-88811719 | Common:5; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88811809-88812395 | Common:6; Rare:210; Clinvar (benign):1 | ||||
| chr16:88812411-88812563 | Common:2; Rare:51 | ||||
| chr16:88856476-88856782 | Common:5; Rare:85; Clinvar (pathogenic):2 | ||||
| chr16:88856841-88857206 | Common:4; Rare:181; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:88857489-88857500 | Rare:3 |