| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88452887-88453381 | Common:3; Rare:183 | ||||
| chr16:88570097-88570503 | Common:2; Rare:155 | ||||
| chr16:88570813-88570920 | Rare:40 | ||||
| chr16:88649934-88650235 | Common:3; Rare:62 | ||||
| chr16:88650341-88650539 | Common:1; Rare:74 | ||||
| chr16:88650575-88650692 | Common:1; Rare:36 | ||||
| chr16:88650946-88651300 | Common:2; Rare:119; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88651434-88651776 | Common:4; Rare:83 | ||||
| chr16:88663018-88663421 | Common:11; Rare:180 | ||||
| chr16:88686131-88686177 | Rare:10 | ||||
| chr16:88686426-88686794 | Common:4; Rare:132 | ||||
| chr16:88700535-88700636 | Common:3; Rare:16 | ||||
| chr16:88700641-88700715 | Common:1; Rare:24 | ||||
| chr16:88700912-88701301 | Common:2; Rare:131 | ||||
| chr16:88703543-88703835 | Common:4; Rare:92 |