Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:141935136-141935201 | Rare:9 | ||||
chr5:141935737-141936083 | Common:4; Rare:66 | ||||
chr5:142003263-142003295 | Rare:9 | ||||
chr5:142803476-142803613 | Common:1; Rare:20 | ||||
chr5:143167343-143167664 | Common:8; Rare:49 | ||||
chr5:143339288-143339366 | Rare:11 | ||||
chr5:143373053-143373081 | Rare:2 | ||||
chr5:143379557-143379745 | Common:1; Rare:33 | ||||
chr5:143394883-143395014 | Rare:26 | ||||
chr5:143398753-143398960 | Rare:32 | ||||
chr5:146063782-146064080 | Common:2; Rare:48 | ||||
chr5:146114765-146115038 | Common:2; Rare:45 | ||||
chr5:146157403-146157792 | Common:1; Rare:100; Clinvar (benign):1 | ||||
chr5:148438485-148438528 | Common:1; Rare:13; Clinvar (benign):2 | ||||
chr5:149549440-149549619 | Rare:39 |