Variant report

Variant rs57826478
Chromosome Location chr6:145586882-145586883
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145579400-145593600 Weak transcription Fetal Kidney kidney
2 chr6:145584200-145587000 Weak transcription Fetal Intestine Small intestine
3 chr6:145584200-145593200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
4 chr6:145585400-145587600 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr6:145585600-145587400 Weak transcription Fetal Brain Male brain
6 chr6:145586000-145588000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:145586200-145587200 Enhancers HepG2 liver
8 chr6:145586200-145588000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr6:145586800-145587200 Enhancers Adipose Nuclei Adipose
10 chr6:145586800-145587800 Enhancers Fetal Intestine Large intestine
11 chr6:145586800-145588800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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