| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86959177-86959453 | Common:1; Rare:50 | ||||
| chr10:86968239-86968552 | Common:5; Rare:71 | ||||
| chr10:87094327-87094442 | Common:1; Rare:27; Clinvar (benign):2 | ||||
| chr10:87094448-87094744 | Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:87094891-87095238 | Common:1; Rare:83; Clinvar:2 | ||||
| chr10:87095600-87095784 | Rare:42 | ||||
| chr10:87504818-87504921 | Common:1; Rare:46 | ||||
| chr10:87659754-87659999 | Common:7; Rare:65 | ||||
| chr10:87818158-87818359 | Common:2; Rare:74 | ||||
| chr10:87863281-87863658 | Common:2; Rare:128; Clinvar:78; Clinvar (benign):8 | ||||
| chr10:87864103-87864544 | Common:1; Rare:131; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr10:88583186-88583424 | Rare:79 | ||||
| chr10:88952711-88952988 | Common:1; Rare:48; Clinvar:1 | ||||
| chr10:88990058-88990283 | Common:2; Rare:29 | ||||
| chr10:88990424-88990947 | Common:6; Rare:137; Clinvar:1; Clinvar (benign):5 |