Variant report

Variant	rs10032594
Chromosome Location	chr4:175645417-175645418
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1352063	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs1485945	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs1485946	0.89[ASN][1000 genomes]
rs17298140	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs17298154	0.90[ASN][1000 genomes]
rs17363787	0.94[CHB][hapmap];0.89[ASN][1000 genomes]
rs1905953	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs1905954	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs2087010	0.95[CHB][hapmap]
rs2332939	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs4695955	0.94[CHB][hapmap]
rs4695956	0.95[CHB][hapmap]
rs60210770	0.90[ASN][1000 genomes]
rs72706187	0.90[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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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