| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:42782725-42782843 | Not yet | Rare:31 | 92 | ||
| chr10:43407751-43407850 | Not yet | Common:1; Rare:41 | 84 | ||
| chr10:43436773-43436903 | Not yet | Common:3; Rare:59 | 91 | ||
| chr10:43606285-43606446 | Not yet | Common:1; Rare:36 | 123 | ||
| chr10:44385084-44385245 | Not yet | Rare:54 | 61 | ||
| chr10:44959561-44959816 | Not yet | Common:2; Rare:79 | 119 | ||
| chr10:44978792-44979047 | Not yet | Common:5; Rare:66 | 166 | ||
| chr10:45000882-45000968 | Not yet | Rare:31 | 68 | ||
| chr10:45727174-45727307 | Not yet | Common:1; Rare:59 | 134 | ||
| chr10:45972355-45972503 | Not yet | Common:1; Rare:41 | 122 | ||
| chr10:49942010-49942073 | Not yet | Rare:12 | 62 | ||
| chr10:50067868-50067979 | Not yet | Common:2; Rare:53 | 129 | ||
| chr10:50418393-50418555 | Not yet | Rare:40 | 146 | ||
| chr10:50990867-50990953 | Not yet | Common:2; Rare:14 | 61 | ||
| chr10:51074397-51074583 | Not yet | Common:1; Rare:44; Clinvar (benign):2 | 104 |