| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15097319-15097387 | Common:1; Rare:32 | ||||
| chr10:15860332-15860573 | Common:1; Rare:62 | ||||
| chr10:16816984-16817229 | Common:1; Rare:74 | ||||
| chr10:17643871-17644305 | Common:2; Rare:133 | ||||
| chr10:18651519-18651955 | Common:2; Rare:142 | ||||
| chr10:18659051-18659584 | Common:4; Rare:163 | ||||
| chr10:21533955-21534236 | Common:1; Rare:104 | ||||
| chr10:22321411-22321600 | Rare:63 | ||||
| chr10:24466244-24466594 | Rare:54 | ||||
| chr10:24607529-24607684 | Rare:39 | ||||
| chr10:25062503-25062792 | Common:1; Rare:47 | ||||
| chr10:26438060-26438455 | Common:2; Rare:95 | ||||
| chr10:26697614-26697964 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:27154310-27154480 | Rare:45 | ||||
| chr10:27155218-27155395 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):4 |