| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87094055-87094292 | Rare:68 | ||||
| chr10:87094321-87094357 | Rare:8 | ||||
| chr10:87094371-87094460 | Common:1; Rare:23; Clinvar (benign):2 | ||||
| chr10:87094518-87094715 | Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:87094891-87095238 | Common:1; Rare:83; Clinvar:2 | ||||
| chr10:87504808-87504966 | Common:1; Rare:80 | ||||
| chr10:87817990-87818359 | Common:2; Rare:119 | ||||
| chr10:87863305-87863666 | Common:2; Rare:121; Clinvar:72; Clinvar (benign):8 | ||||
| chr10:87864132-87864551 | Common:1; Rare:128; Clinvar:19; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr10:88583290-88583372 | Rare:13 | ||||
| chr10:88880401-88880557 | Common:1; Rare:28 | ||||
| chr10:88952679-88952790 | Rare:17; Clinvar:1 | ||||
| chr10:88990276-88990283 | |||||
| chr10:88990453-88990815 | Common:4; Rare:101; Clinvar (benign):4 | ||||
| chr10:88990822-88990900 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 |