Variant report

Variant	rs4597807
Chromosome Location	chr4:47344313-47344314
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10000697	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10023965	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10440176	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs1076015	0.93[JPT][hapmap]
rs11731871	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs11737184	0.86[ASN][1000 genomes]
rs12331018	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs12500794	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12503495	0.84[CEU][hapmap]
rs13104400	0.96[CEU][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13108343	0.84[CEU][hapmap]
rs17461709	0.83[CEU][hapmap]
rs17600296	0.85[JPT][hapmap]
rs17600330	0.85[JPT][hapmap]
rs34098612	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34429982	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35744755	0.85[JPT][hapmap]
rs3822112	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs4261959	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4261968	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4302438	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs4386575	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4396966	0.93[JPT][hapmap]
rs4495018	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4508859	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4577548	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4588429	0.95[CEU][hapmap];0.82[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4599390	0.87[CHB][hapmap];0.93[JPT][hapmap];0.81[YRI][hapmap]
rs4602475	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4695209	0.85[JPT][hapmap]
rs55825318	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56336915	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62297800	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6447546	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6820498	1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6831556	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6833189	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6837135	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7659625	0.83[ASN][1000 genomes]
rs7664909	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7665508	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7666958	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7674333	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7683663	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7683676	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7687439	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9291305	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9917915	0.90[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[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	nsv998919	chr4:47207023-47476876	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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
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