Variant report

Variant rs58884332
Chromosome Location chr1:77459531-77459532
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77456200-77460400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:77456400-77460600 Weak transcription NHEK skin
3 chr1:77456800-77472400 Weak transcription Aorta Aorta
4 chr1:77458400-77460200 Enhancers Cortex derived primary cultured neurospheres brain
5 chr1:77458600-77459800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:77458800-77459600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:77458800-77459600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:77458800-77459600 Enhancers NHDF-Ad bronchial
9 chr1:77459000-77459600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr1:77459000-77460400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr1:77459400-77464000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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