Variant report

Variant	rs1388891
Chromosome Location	chr4:167458731-167458732
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10003435	0.92[EUR][1000 genomes]
rs10011001	0.94[EUR][1000 genomes]
rs10011514	0.94[EUR][1000 genomes]
rs10031526	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10033185	0.94[EUR][1000 genomes]
rs10033695	0.94[EUR][1000 genomes]
rs11100655	0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11100656	0.98[EUR][1000 genomes]
rs11941377	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs11941399	0.98[EUR][1000 genomes]
rs1388892	0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1492537	1.00[CEU][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs17691801	0.98[EUR][1000 genomes]
rs28520116	0.96[EUR][1000 genomes]
rs28721430	0.98[EUR][1000 genomes]
rs28814323	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs28825396	0.94[EUR][1000 genomes]
rs55764102	0.89[EUR][1000 genomes]
rs55827333	0.89[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs55938252	0.89[EUR][1000 genomes]
rs56363227	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56988749	0.85[EUR][1000 genomes]
rs57062088	0.85[EUR][1000 genomes]
rs58560983	0.86[ASN][1000 genomes]
rs59648329	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60352657	0.88[ASN][1000 genomes]
rs60862221	0.82[ASN][1000 genomes]
rs60954953	0.98[EUR][1000 genomes]
rs6536969	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs67022962	0.94[EUR][1000 genomes]
rs6810663	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6810863	0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6812925	0.94[EUR][1000 genomes]
rs6818099	0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6838571	0.82[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6838761	0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6842356	1.00[CEU][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs6849480	1.00[CEU][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72974129	0.83[ASN][1000 genomes]
rs7656812	0.94[EUR][1000 genomes]
rs7662275	0.83[ASN][1000 genomes]
rs7675098	0.82[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs7675522	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs7683316	0.83[ASN][1000 genomes]
rs7691729	0.92[EUR][1000 genomes]
rs875441	0.87[ASW][hapmap];1.00[CEU][hapmap];0.84[GIH][hapmap];0.81[LWK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9684759	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9686050	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9991455	0.94[EUR][1000 genomes]
rs9991542	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034421	chr4:166961339-167893289	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv537339	chr4:166961339-167893289	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv881405	chr4:167193885-167628013	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1023051	chr4:167304814-168211540	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv537340	chr4:167304814-168211540	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv881309	chr4:167377133-167500233	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv830143	chr4:167386232-167538014	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1017028	chr4:167420519-167697787	Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1035039	chr4:167455577-167521841	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167449000-167459600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:167457600-167459600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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