| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88504990-88505215 | Common:2; Rare:118 | ||||
| chr16:88759251-88759587 | Common:6; Rare:141 | ||||
| chr16:88819130-88819410 | Common:4; Rare:66 | ||||
| chr16:89191120-89191450 | Common:1; Rare:227 | ||||
| chr16:89240928-89241349 | Common:8; Rare:148 | ||||
| chr16:89247289-89247758 | Common:7; Rare:348 | ||||
| chr16:89505448-89505716 | Common:2; Rare:127 | ||||
| chr16:89622030-89622364 | Common:6; Rare:105 | ||||
| chr16:89694712-89695045 | Common:4; Rare:300; Clinvar (pathogenic):1 | ||||
| chr16:89822445-89822823 | Rare:150 | ||||
| chr16:89837630-89838110 | Common:8; Rare:235 | ||||
| chr17:488820-489370 | Rare:61 | ||||
| chr17:937150-937870 | Common:16; Rare:149 | ||||
| chr17:1597910-1598180 | Common:4; Rare:64 | ||||
| chr17:1714621-1715021 | Common:6; Rare:169 |