| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86521737-86521947 | Rare:68 | ||||
| chr10:86756268-86756626 | Common:4; Rare:123 | ||||
| chr10:86957548-86957781 | Rare:58 | ||||
| chr10:86958493-86958659 | Rare:49 | ||||
| chr10:86968175-86968604 | Common:5; Rare:104 | ||||
| chr10:86969931-86970261 | Rare:77 | ||||
| chr10:87094055-87094305 | Rare:73 | ||||
| chr10:87094314-87094468 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr10:87094518-87094663 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:87094857-87095235 | Common:1; Rare:90; Clinvar:3 | ||||
| chr10:87504808-87505137 | Common:1; Rare:161; Clinvar (pathogenic):1 | ||||
| chr10:87818154-87818312 | Rare:58 | ||||
| chr10:87863301-87863656 | Common:2; Rare:118; Clinvar:70; Clinvar (benign):8 | ||||
| chr10:88583196-88583402 | Rare:65 | ||||
| chr10:88952731-88952950 | Rare:32; Clinvar:1 |