| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70887680-70887980 | Common:3; Rare:84 | ||||
| chr10:70888527-70888683 | Common:4; Rare:98; Clinvar:10; Clinvar (benign):4 | ||||
| chr10:71212355-71212769 | Common:3; Rare:207 | ||||
| chr10:71851199-71851454 | Common:10; Rare:200; Clinvar:7; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
| chr10:71964116-71964580 | Common:9; Rare:228; Clinvar:2; Clinvar (benign):6 | ||||
| chr10:72088410-72088950 | Common:4; Rare:149 | ||||
| chr10:72216230-72216336 | Rare:101 | ||||
| chr10:72273613-72274069 | Rare:226 | ||||
| chr10:72354451-72354851 | Common:1; Rare:170 | ||||
| chr10:72354886-72355054 | Common:3; Rare:149 | ||||
| chr10:72523848-72524239 | Common:2; Rare:132 | ||||
| chr10:72626017-72626321 | Common:2; Rare:135 | ||||
| chr10:72954688-72954918 | Common:1; Rare:44 | ||||
| chr10:73096729-73097187 | Common:7; Rare:171 | ||||
| chr10:73110391-73110545 | Rare:31 |