Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:42782725-42782843 | Rare:31 | ||||
chr10:43407751-43407850 | Common:1; Rare:41 | ||||
chr10:43436773-43436903 | Common:3; Rare:59 | ||||
chr10:43606285-43606446 | Common:1; Rare:36 | ||||
chr10:44385084-44385245 | Rare:54 | ||||
chr10:44959561-44959816 | Common:2; Rare:79 | ||||
chr10:44978792-44979047 | Common:5; Rare:66 | ||||
chr10:45000882-45000968 | Rare:31 | ||||
chr10:45727174-45727307 | Common:1; Rare:59 | ||||
chr10:45972355-45972503 | Common:1; Rare:41 | ||||
chr10:49942010-49942073 | Rare:12 | ||||
chr10:50067868-50067979 | Common:2; Rare:53 | ||||
chr10:50418393-50418555 | Rare:40 | ||||
chr10:50990867-50990953 | Common:2; Rare:14 | ||||
chr10:51074397-51074583 | Common:1; Rare:44; Clinvar (benign):2 |