Variant report

Variant	rs11186638
Chromosome Location	chr10:93397014-93397015
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93393400-93403600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:93393600-93397200	Enhancers	Liver	Liver
3	chr10:93393600-93402800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:93395400-93397200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr10:93395600-93397200	Weak transcription	Adipose Nuclei	Adipose
6	chr10:93395800-93402000	Weak transcription	Aorta	Aorta
7	chr10:93395800-93402800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:93396000-93399400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:93396800-93397800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:93396800-93401600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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