Variant report

Variant	rs192167018
Chromosome Location	chr10:118627522-118627523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv971856	chr10:118626730-118630578	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118621800-118628800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr10:118623600-118628800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:118626600-118628200	Enhancers	NHEK	skin
4	chr10:118627000-118628000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:118627000-118628000	Enhancers	Liver	Liver
6	chr10:118627000-118628000	Weak transcription	Fetal Brain Male	brain
7	chr10:118627000-118628200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:118627400-118627600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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