| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86555172-86555256 | Rare:45 | ||||
| chr16:87317376-87317508 | Common:4; Rare:52 | ||||
| chr16:87762511-87762812 | Rare:101 | ||||
| chr16:87765878-87766044 | Rare:66 | ||||
| chr16:87951124-87951506 | Common:2; Rare:132 | ||||
| chr16:88570179-88570482 | Common:1; Rare:117 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88706251-88706522 | Common:4; Rare:125 | ||||
| chr16:88725447-88725776 | Common:3; Rare:164; Clinvar (benign):2 | ||||
| chr16:88811895-88812052 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr16:88856901-88857177 | Common:4; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89093742-89093943 | Common:5; Rare:88 | ||||
| chr16:89217619-89217738 | Common:1; Rare:56 | ||||
| chr16:89508280-89508493 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560717 | Rare:73 |