Variant report

Variant	rs11690457
Chromosome Location	chr2:34403096-34403097
allele	A/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:41)

rs_ID	r²[population]
rs10170231	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10173562	0.83[ASN][1000 genomes]
rs10174698	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10176113	0.88[ASN][1000 genomes]
rs10197054	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10210068	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10210837	0.88[ASN][1000 genomes]
rs11124365	0.83[ASN][1000 genomes]
rs12617181	0.83[ASN][1000 genomes]
rs13421243	0.88[ASN][1000 genomes]
rs17014921	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17432481	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1987712	0.83[ASN][1000 genomes]
rs1990838	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2193805	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2193806	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2371924	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2371930	0.96[ASN][1000 genomes]
rs2888194	0.88[ASN][1000 genomes]
rs2888196	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4316922	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4670076	0.88[ASN][1000 genomes]
rs4670077	0.88[ASN][1000 genomes]
rs4670078	0.88[ASN][1000 genomes]
rs4670079	0.88[ASN][1000 genomes]
rs4670080	0.88[ASN][1000 genomes]
rs4670333	0.92[ASN][1000 genomes]
rs4670339	0.88[ASN][1000 genomes]
rs4670340	0.88[ASN][1000 genomes]
rs4670341	0.88[ASN][1000 genomes]
rs5023564	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5023565	0.88[ASN][1000 genomes]
rs5023566	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5023567	0.88[ASN][1000 genomes]
rs6707565	0.80[ASN][1000 genomes]
rs6719943	0.84[AMR][1000 genomes]
rs6725420	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6751907	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7557064	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7595827	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9973481	0.83[ASN][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	nsv1006001	chr2:33991364-34858721	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv535628	chr2:33991364-34858721	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv873798	chr2:33996983-34410240	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv873799	chr2:33996983-34821990	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv999091	chr2:34154486-34993188	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv535629	chr2:34154486-34993188	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv873804	chr2:34156867-35047107	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv873808	chr2:34275757-34703057	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1012401	chr2:34302403-34468097	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv833714	chr2:34348193-34504892	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv522079	chr2:34398738-34403344	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34403000-34403800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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