| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70785321-70785484 | Rare:22 | ||||
| chr10:70815842-70816050 | Rare:82 | ||||
| chr10:70888229-70888272 | Rare:13 | ||||
| chr10:70888530-70888665 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:71319147-71319296 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71773472-71773681 | Common:2; Rare:67 | ||||
| chr10:71797076-71797302 | Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:71819463-71819897 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:71822043-71822146 | Common:2; Rare:24 | ||||
| chr10:71850766-71851395 | Common:5; Rare:229; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:72216205-72216630 | Common:3; Rare:112 | ||||
| chr10:72273659-72273953 | Rare:78 | ||||
| chr10:72354576-72354725 | Rare:44 | ||||
| chr10:72354769-72355206 | Common:3; Rare:154 | ||||
| chr10:72626029-72626361 | Common:2; Rare:80 |