Variant report

Variant	rs1835543
Chromosome Location	chr3:88058387-88058388
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10511136	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11128018	0.83[EUR][1000 genomes]
rs11128019	0.83[EUR][1000 genomes]
rs11717021	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11717413	0.86[EUR][1000 genomes]
rs11915058	0.83[EUR][1000 genomes]
rs12714696	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13074576	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1431153	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1469569	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1503433	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1604699	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17025236	0.87[ASN][1000 genomes]
rs17025241	0.88[ASN][1000 genomes]
rs17549213	0.84[EUR][1000 genomes]
rs17549345	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1835542	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2016224	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2082226	0.83[ASN][1000 genomes]
rs2099229	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2163423	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2344185	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2880801	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2880802	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35040143	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858925	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4858969	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4858971	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858972	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4858974	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858975	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55840331	0.84[EUR][1000 genomes]
rs56323967	0.83[ASN][1000 genomes]
rs58658187	0.88[ASN][1000 genomes]
rs60099577	0.83[EUR][1000 genomes]
rs67047416	0.83[EUR][1000 genomes]
rs67566069	0.88[ASN][1000 genomes]
rs6770013	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6778211	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6781226	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6781901	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6785333	0.85[EUR][1000 genomes]
rs6787253	0.88[ASN][1000 genomes]
rs6789002	0.82[EUR][1000 genomes]
rs6798161	0.87[ASN][1000 genomes]
rs68042814	0.83[EUR][1000 genomes]
rs6804848	0.88[ASN][1000 genomes]
rs68068970	0.87[ASN][1000 genomes]
rs73140133	0.88[ASN][1000 genomes]
rs73140134	0.86[ASN][1000 genomes]
rs7629565	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7630716	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7637503	0.87[EUR][1000 genomes]
rs7652406	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9310061	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9681975	0.88[ASN][1000 genomes]
rs9852704	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs9855839	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9859034	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs9861809	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9863076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9878862	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9880480	0.82[EUR][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	nsv877146	chr3:87983962-88159835	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
2	nsv536635	chr3:88049304-88088520	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88054600-88059000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:88057800-88058600	Enhancers	Primary B cells from peripheral blood	blood

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