Variant report

Variant	rs4673436
Chromosome Location	chr2:209854899-209854900
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10173310	1.00[ASN][1000 genomes]
rs10184732	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10196945	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10204059	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10205030	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208392	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10932279	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11884309	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12624051	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13394260	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13406876	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16841989	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16841996	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16842003	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3851942	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4289122	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4673432	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73986657	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7589445	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7603010	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9989855	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460058	chr2:209755059-209866395	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv584306	chr2:209755059-209866395	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1012184	chr2:209755847-210049331	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536131	chr2:209755847-210049331	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv3487576	chr2:209768379-209947296	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3487577	chr2:209768379-209947296	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1009924	chr2:209805661-210042572	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv875760	chr2:209817526-209929978	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1002578	chr2:209836205-210026339	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv536132	chr2:209836205-210026339	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209851200-209856800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:209853800-209855000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:209854200-209855800	Weak transcription	Fetal Brain Male	brain

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