Variant report

Variant	rs34515056
Chromosome Location	chr3:61198019-61198020
allele	C/T
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:41)

rs_ID	r²[population]
rs11130821	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11130822	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11130826	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11130827	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11720254	0.82[EUR][1000 genomes]
rs12492551	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1524017	0.84[ASN][1000 genomes]
rs1554599	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs17064630	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs17064660	0.82[ASN][1000 genomes]
rs1916800	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1916801	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1916802	0.80[EUR][1000 genomes]
rs1980308	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1980309	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1980310	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1980311	0.82[EUR][1000 genomes]
rs35198002	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs3915074	0.84[ASN][1000 genomes]
rs4296587	0.80[EUR][1000 genomes]
rs4535219	0.80[EUR][1000 genomes]
rs4605537	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4688354	0.81[EUR][1000 genomes]
rs4688355	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4688359	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4688379	0.83[EUR][1000 genomes]
rs6445197	0.81[EUR][1000 genomes]
rs6445198	0.81[EUR][1000 genomes]
rs6445199	0.81[EUR][1000 genomes]
rs6787292	0.82[EUR][1000 genomes]
rs6809031	0.80[EUR][1000 genomes]
rs71296711	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7432943	0.83[AFR][1000 genomes]
rs9843007	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9844741	0.80[EUR][1000 genomes]
rs9846073	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9850114	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9859004	0.80[EUR][1000 genomes]
rs9860681	0.85[AFR][1000 genomes]
rs9875827	0.80[EUR][1000 genomes]
rs9882800	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv876866	chr3:61054494-61310328	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv876867	chr3:61054494-61474575	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv432423	chr3:61100255-61606060	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1000378	chr3:61103229-61238089	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv2756994	chr3:61144427-61220809	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv876868	chr3:61145050-61282503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv532626	chr3:61159646-61388418	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv997718	chr3:61176349-61222975	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
10	nsv1008399	chr3:61176965-61461349	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv3323408	chr3:61194212-61199410	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:61172400-61203000	Weak transcription	Pancreas	Pancrea
2	chr3:61197600-61203000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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