Variant report

Variant	rs58781739
Chromosome Location	chr5:68134005-68134006
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68131200-68134800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:68131200-68135200	Weak transcription	Adipose Nuclei	Adipose
3	chr5:68131400-68134200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:68131400-68134200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:68133000-68142800	Weak transcription	Aorta	Aorta
6	chr5:68133600-68136800	Enhancers	Placenta Amnion	Placenta Amnion
7	chr5:68133800-68134200	Enhancers	Brain Hippocampus Middle	brain
8	chr5:68133800-68134400	Enhancers	Brain Angular Gyrus	brain
9	chr5:68134000-68135200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:68134000-68135600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:68134000-68135600	Enhancers	NHDF-Ad	bronchial

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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