| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:71851007-71851087 | Rare:28 | ||||
| chr10:71851143-71851488 | Common:5; Rare:131; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:71964131-71964257 | Common:1; Rare:43 | ||||
| chr10:71964471-71964557 | Common:3; Rare:22; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:71964698-71964807 | Common:1; Rare:28 | ||||
| chr10:72215840-72216134 | Rare:105 | ||||
| chr10:72216212-72216419 | Rare:78 | ||||
| chr10:72273401-72274122 | Common:2; Rare:181 | ||||
| chr10:72354315-72354803 | Common:2; Rare:117 | ||||
| chr10:72354880-72355253 | Common:2; Rare:126 | ||||
| chr10:72625944-72626411 | Common:2; Rare:104 | ||||
| chr10:72691979-72692206 | Rare:79 | ||||
| chr10:72692421-72692569 | Rare:33 | ||||
| chr10:73096105-73096410 | Common:1; Rare:84 | ||||
| chr10:73096804-73096921 | Common:2; Rare:38 |