Variant report

Variant	rs2347635
Chromosome Location	chr6:71699928-71699929
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10945278	0.82[AMR][1000 genomes]
rs11757574	0.82[AMR][1000 genomes]
rs11759339	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs12529422	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16869607	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs2347632	0.83[AMR][1000 genomes]
rs2347633	0.83[AMR][1000 genomes]
rs4479893	0.83[AMR][1000 genomes]
rs4506005	0.83[AMR][1000 genomes]
rs55870610	0.82[AMR][1000 genomes]
rs56291137	0.83[AMR][1000 genomes]
rs6907179	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs6911809	1.00[CHB][hapmap]
rs7451863	0.82[AMR][1000 genomes]
rs7746949	0.83[AMR][1000 genomes]
rs7774025	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs9283838	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9294883	0.83[AMR][1000 genomes]
rs9354961	1.00[CHB][hapmap]
rs9446317	0.81[ASN][1000 genomes]
rs9455286	0.81[ASN][1000 genomes]
rs9455291	0.81[ASN][1000 genomes]

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	nsv966627	chr6:71699692-71726851	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71695600-71716600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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

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