Variant report

Variant rs376576539
Chromosome Location chr5:178925586-178925587
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178913800-178935200 Weak transcription Right Atrium heart
2 chr5:178922200-178931400 Weak transcription Pancreas Pancrea
3 chr5:178924600-178925600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr5:178924800-178925600 Enhancers Fetal Brain Female brain
5 chr5:178924800-178925600 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr5:178924800-178925600 Enhancers NHDF-Ad bronchial
7 chr5:178925000-178925600 Enhancers Adipose Nuclei Adipose
8 chr5:178925200-178925600 Active TSS Spleen Spleen
9 chr5:178925400-178925600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr5:178925400-178925800 Enhancers Esophagus oesophagus

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