Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12795743	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12797437	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12800678	1.00[ASN][1000 genomes]
rs12801760	1.00[ASN][1000 genomes]
rs12807118	1.00[ASN][1000 genomes]
rs12807207	1.00[ASN][1000 genomes]
rs12808035	1.00[ASN][1000 genomes]
rs17633182	1.00[ASN][1000 genomes]
rs17633211	1.00[ASN][1000 genomes]
rs17633229	1.00[ASN][1000 genomes]
rs17633258	1.00[ASN][1000 genomes]
rs17706299	1.00[ASN][1000 genomes]
rs17706334	1.00[ASN][1000 genomes]
rs17706358	1.00[ASN][1000 genomes]
rs17706480	1.00[ASN][1000 genomes]
rs17706512	1.00[ASN][1000 genomes]
rs1876858	1.00[ASN][1000 genomes]
rs2136537	1.00[ASN][1000 genomes]
rs2136538	1.00[ASN][1000 genomes]
rs34356994	1.00[ASN][1000 genomes]
rs34930115	1.00[ASN][1000 genomes]
rs35335615	1.00[ASN][1000 genomes]
rs35540887	1.00[ASN][1000 genomes]
rs35974851	1.00[ASN][1000 genomes]
rs4082792	1.00[ASN][1000 genomes]
rs71475130	1.00[ASN][1000 genomes]
rs7938477	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv898390	chr11:108893765-109003536	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr11:108962600-108964400	Enhancers	Fetal Heart	heart

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