| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:71821982-71822146 | Common:2; Rare:39; Clinvar:1 | ||||
| chr10:71851156-71851465 | Common:5; Rare:126; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:71964209-71964572 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:72216227-72216535 | Common:3; Rare:91 | ||||
| chr10:72273698-72274040 | Rare:106 | ||||
| chr10:72354782-72355184 | Common:2; Rare:142 | ||||
| chr10:72691964-72692151 | Rare:50 | ||||
| chr10:72692810-72693114 | Common:2; Rare:91 | ||||
| chr10:73096764-73097022 | Common:3; Rare:80 | ||||
| chr10:73097082-73097152 | Common:1; Rare:13 | ||||
| chr10:73110228-73110534 | Rare:55 | ||||
| chr10:73167958-73168153 | Rare:48 | ||||
| chr10:73252589-73252802 | Rare:58; Clinvar:4 | ||||
| chr10:73414011-73414195 | Common:3; Rare:53 | ||||
| chr10:73495595-73495805 | Rare:54 |