| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:92574003-92574366 | Common:2; Rare:107 | ||||
| chr10:92592952-92593169 | Common:3; Rare:63 | ||||
| chr10:93482213-93482358 | Common:2; Rare:42 | ||||
| chr10:93482362-93482466 | Rare:24 | ||||
| chr10:93702380-93702708 | Common:5; Rare:109 | ||||
| chr10:93757670-93758039 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:94362897-94363034 | Common:3; Rare:57 | ||||
| chr10:95290912-95291194 | Common:2; Rare:115 | ||||
| chr10:95693891-95694098 | Common:4; Rare:71; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:95907773-95907940 | Common:2; Rare:51 | ||||
| chr10:96129662-96129732 | Common:1; Rare:22 | ||||
| chr10:96129988-96130558 | Common:5; Rare:189 | ||||
| chr10:96832014-96832318 | Rare:116 | ||||
| chr10:97426037-97426283 | Common:2; Rare:103 | ||||
| chr10:97445981-97446210 | Rare:59 |