| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:85220312-85220581 | Rare:95 | ||||
| chr8:85220690-85220960 | Rare:47 | ||||
| chr8:85463160-85463450 | Common:5; Rare:66 | ||||
| chr8:86342319-86342652 | Common:1; Rare:105 | ||||
| chr8:86508598-86508955 | Common:3; Rare:126 | ||||
| chr8:86514304-86514481 | Common:1; Rare:43 | ||||
| chr8:88326723-88327123 | Rare:135 | ||||
| chr8:88327284-88327412 | Rare:25 | ||||
| chr8:88327527-88327921 | Common:11; Rare:156 | ||||
| chr8:89757287-89757483 | Common:1; Rare:60 | ||||
| chr8:89757635-89757879 | Common:1; Rare:90 | ||||
| chr8:89901756-89902156 | Common:4; Rare:196 | ||||
| chr8:89902345-89902651 | Common:2; Rare:112 | ||||
| chr8:89984108-89984369 | Common:1; Rare:60 | ||||
| chr8:89984553-89984795 | Rare:83; Clinvar:3; Clinvar (benign):16; Clinvar (pathogenic):2 |