Variant report

Variant rs1415808
Chromosome Location chr6:145588073-145588074
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145579400-145593600 Weak transcription Fetal Kidney kidney
2 chr6:145584200-145593200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
3 chr6:145586800-145588800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr6:145587000-145589000 Enhancers Fetal Intestine Small intestine
5 chr6:145587200-145588200 Flanking Active TSS HepG2 liver
6 chr6:145587200-145588400 Enhancers Rectal Mucosa Donor 31 rectum
7 chr6:145587200-145588600 Enhancers Liver Liver
8 chr6:145587600-145588600 Enhancers Pancreatic Islets Pancreatic Islet
9 chr6:145587600-145589200 Enhancers Stomach Mucosa stomach
10 chr6:145587600-145589800 Enhancers Adipose Nuclei Adipose
11 chr6:145587800-145588800 Weak transcription Fetal Brain Male brain
12 chr6:145587800-145591200 Weak transcription Fetal Intestine Large intestine
13 chr6:145588000-145588400 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr6:145588000-145588600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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