Variant report

Variant	rs11098882
Chromosome Location	chr4:127447572-127447573
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11098881	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12650060	0.97[ASN][1000 genomes]
rs28558216	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs56358919	0.96[ASN][1000 genomes]
rs57902647	0.86[ASN][1000 genomes]
rs59819551	0.95[ASN][1000 genomes]
rs61359035	0.96[ASN][1000 genomes]
rs7687335	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7687529	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7687807	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7687848	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7691736	0.85[AFR][1000 genomes];0.97[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	nsv595385	chr4:127383473-127451806	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127447200-127448400	ZNF genes & repeats	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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