Variant report

Variant	rs59929156
Chromosome Location	chr7:104296874-104296875
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10231269	0.83[EUR][1000 genomes]
rs10280659	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11762558	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11773248	0.97[EUR][1000 genomes]
rs17139574	0.90[ASN][1000 genomes]
rs2193212	0.95[EUR][1000 genomes]
rs35022976	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73181816	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73181817	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7805947	0.84[EUR][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	nsv1024532	chr7:104281393-104299847	Enhancers Bivalent Enhancer Active TSS Weak transcription 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	chr7:104296800-104297200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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