Variant report

Variant	rs11068443
Chromosome Location	chr12:117744015-117744016
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11068418	1.00[TSI][hapmap]
rs2293044	1.00[TSI][hapmap]
rs3782214	1.00[TSI][hapmap]
rs9658280	1.00[TSI][hapmap]

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	esv3375737	chr12:117741490-117744384	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117697200-117746200	Weak transcription	Brain Anterior Caudate	brain
2	chr12:117728000-117771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr12:117732600-117747000	Weak transcription	NHEK	skin
4	chr12:117735000-117748000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:117739800-117771400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:117740000-117756400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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