Variant report

Variant	rs2086766
Chromosome Location	chr4:125785028-125785029
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11725383	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11729757	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11729760	1.00[ASN][1000 genomes]
rs28617665	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59349224	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62323269	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62323271	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323272	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323273	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323299	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6816885	0.82[ASN][1000 genomes]
rs6843692	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7695725	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011752	chr4:125708756-125932456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv830050	chr4:125717858-125888563	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125781600-125785400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:125782400-125786200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:125784000-125787200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:125784000-125788400	Weak transcription	HSMMtube	muscle
5	chr4:125784400-125787400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:125784400-125788000	Weak transcription	Osteobl	bone
7	chr4:125784600-125787200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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