Variant report

Variant	rs17040606
Chromosome Location	chr2:50635131-50635132
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10204268	0.90[ASN][1000 genomes]
rs10208208	0.84[CEU][hapmap]
rs10210298	0.95[CHB][hapmap];0.96[JPT][hapmap];0.94[ASN][1000 genomes]
rs10490230	0.84[CEU][hapmap]
rs10490231	0.82[CEU][hapmap]
rs11903097	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12053271	0.82[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12463670	0.82[CEU][hapmap]
rs12474009	1.00[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap]
rs12616829	0.89[ASN][1000 genomes]
rs12616901	0.89[ASN][1000 genomes]
rs12620185	0.87[ASN][1000 genomes]
rs13404855	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs13407780	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1402121	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1402168	0.84[CEU][hapmap]
rs1520445	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1520451	0.82[CEU][hapmap]
rs1543973	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs17040490	0.95[CHB][hapmap];0.96[JPT][hapmap]
rs17040542	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs17040552	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs17466651	0.82[CEU][hapmap]
rs1814972	0.84[CEU][hapmap]
rs1879320	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap]
rs1915170	0.82[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs1915171	0.84[CEU][hapmap]
rs1915172	0.81[CHB][hapmap];0.96[JPT][hapmap];0.90[ASN][1000 genomes]
rs1969351	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1972311	0.94[CEU][hapmap];0.81[CHB][hapmap];0.96[JPT][hapmap]
rs2139629	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2176853	1.00[CHB][hapmap];0.96[JPT][hapmap]
rs2176854	0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs2176855	1.00[CHB][hapmap];0.96[JPT][hapmap];0.96[ASN][1000 genomes]
rs2882692	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4450643	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4493303	0.81[JPT][hapmap]
rs4971557	0.90[CHB][hapmap];0.96[JPT][hapmap];0.92[ASN][1000 genomes]
rs4971668	0.95[ASN][1000 genomes]
rs4971670	0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs5019239	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs6727675	0.85[ASN][1000 genomes]
rs7560420	0.81[CHB][hapmap];0.96[JPT][hapmap]
rs7560724	1.00[CHB][hapmap];0.96[JPT][hapmap]
rs7575728	0.90[CHB][hapmap];0.96[JPT][hapmap]
rs7599052	1.00[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948548	chr2:50569117-50695100	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv948361	chr2:50611076-50785178	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv933786	chr2:50628354-50780185	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 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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