| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87817883-87818339 | Common:1; Rare:145 | ||||
| chr10:87864139-87864431 | Rare:95; Clinvar:3; Clinvar (benign):7 | ||||
| chr10:88583196-88583266 | Rare:29 | ||||
| chr10:88583290-88583348 | Rare:8 | ||||
| chr10:88952731-88953033 | Common:2; Rare:54; Clinvar:1 | ||||
| chr10:88990432-88990882 | Common:6; Rare:119; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:88991310-88991470 | Common:3; Rare:29 | ||||
| chr10:89301869-89302079 | Rare:44 | ||||
| chr10:89332241-89332580 | Common:3; Rare:63 | ||||
| chr10:89414289-89414627 | Common:4; Rare:68 | ||||
| chr10:89414665-89414801 | Common:3; Rare:71 | ||||
| chr10:89643886-89644149 | Rare:52 | ||||
| chr10:89644978-89645291 | Common:3; Rare:140 | ||||
| chr10:89701391-89701662 | Common:2; Rare:87 | ||||
| chr10:90920903-90921298 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):4 |