| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34381566-34381792 | Rare:36 | ||||
| chr9:34458518-34458840 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34637725-34637943 | Rare:64 | ||||
| chr9:34652015-34652217 | Rare:58 | ||||
| chr9:34665373-34665655 | Rare:92 | ||||
| chr9:34666021-34666139 | Common:1; Rare:24 | ||||
| chr9:34990040-34990273 | Rare:62 | ||||
| chr9:35072004-35072309 | Rare:107 | ||||
| chr9:35103080-35103320 | Common:1; Rare:82 | ||||
| chr9:35489922-35490139 | Common:2; Rare:61 | ||||
| chr9:35657724-35657816 | Common:2; Rare:73; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr9:35657834-35658496 | Common:12; Rare:489; Clinvar:44; Clinvar (benign):17; Clinvar (pathogenic):40 | ||||
| chr9:35689697-35690136 | Common:4; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690595-35690914 | Rare:64 | ||||
| chr9:35691057-35691274 | Common:1; Rare:47 |