Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:135334975-135335274 | Common:4; Rare:76 | ||||
chr5:136080595-136080696 | Rare:35 | ||||
chr5:137146626-137146738 | Rare:18 | ||||
chr5:137753170-137753225 | Rare:16 | ||||
chr5:138464676-138464873 | Rare:51 | ||||
chr5:138519232-138519382 | Common:1; Rare:22 | ||||
chr5:138571007-138571322 | Common:2; Rare:78 | ||||
chr5:138933662-138933908 | Common:1; Rare:57; Clinvar (benign):1 | ||||
chr5:140269949-140270220 | Common:1; Rare:31 | ||||
chr5:140711130-140711314 | Common:1; Rare:56 | ||||
chr5:141445029-141445244 | Rare:40 | ||||
chr5:141604561-141604591 | Rare:4 | ||||
chr5:142357034-142357239 | Common:1; Rare:76 | ||||
chr5:142438725-142438879 | Rare:27 | ||||
chr5:142931901-142932083 | Common:1; Rare:45 |