| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317394-87317516 | Common:2; Rare:45 | ||||
| chr16:87765919-87766062 | Common:1; Rare:58 | ||||
| chr16:88570179-88570467 | Common:1; Rare:110 | ||||
| chr16:88650967-88651177 | Common:1; Rare:68; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88663070-88663382 | Common:9; Rare:130 | ||||
| chr16:88706264-88706522 | Common:4; Rare:118 | ||||
| chr16:88856891-88857163 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89093779-89093931 | Common:3; Rare:67 | ||||
| chr16:89217627-89217749 | Common:1; Rare:54 | ||||
| chr16:89508241-89508424 | Common:1; Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560725 | Rare:89 | ||||
| chr16:89657647-89658103 | Common:3; Rare:238 | ||||
| chr16:89686573-89686706 | Common:6; Rare:61 | ||||
| chr16:89720857-89720999 | Common:1; Rare:37 | ||||
| chr16:89873316-89873856 | Common:7; Rare:234 |