Variant report

Variant	rs7587134
Chromosome Location	chr2:37651922-37651923
allele	C/T
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]
rs10173794	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617664	0.95[ASN][1000 genomes]
rs12620578	0.95[ASN][1000 genomes]
rs13425396	0.83[AFR][1000 genomes]
rs17020706	0.94[ASN][1000 genomes]
rs2058717	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4670704	0.81[EUR][1000 genomes]
rs4670708	0.96[ASN][1000 genomes]
rs56107750	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59560107	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59966191	0.81[ASN][1000 genomes]
rs72792867	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	nsv833814	chr2:37643132-37840247	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37651800-37654400	Enhancers	Fetal Heart	heart

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

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