Variant report

Variant rs566348364
Chromosome Location chr5:177694237-177694238
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177669800-177699200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr5:177683000-177697400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr5:177689400-177698000 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr5:177693000-177694800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177693400-177695000 Enhancers Fetal Heart heart
6 chr5:177693600-177695400 Enhancers Right Ventricle heart
7 chr5:177694000-177694400 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle
8 chr5:177694000-177695000 Enhancers Skeletal Muscle Female skeletal muscle
9 chr5:177694000-177695200 Enhancers Left Ventricle heart
10 chr5:177694000-177696800 Weak transcription Fetal Stomach stomach

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