Variant report

Variant	rs7109075
Chromosome Location	chr11:106742577-106742578
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11211920	0.84[ASN][1000 genomes]
rs11211938	0.81[ASN][1000 genomes]
rs11211945	0.95[ASN][1000 genomes]
rs11524439	0.84[ASN][1000 genomes]
rs12363827	0.81[ASN][1000 genomes]
rs12364559	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12364578	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1487890	0.84[ASN][1000 genomes]
rs1944195	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs33916298	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35636240	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67110749	0.95[ASN][1000 genomes]
rs7113801	0.83[ASN][1000 genomes]
rs7950351	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898362	chr11:106715879-106809457	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1036990	chr11:106718613-106774766	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv541162	chr11:106718613-106774766	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv556231	chr11:106737224-106815963	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	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	chr11:106742400-106742800	Flanking Active TSS	Fetal Heart	heart

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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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