Variant report

Variant	rs6822408
Chromosome Location	chr4:119050333-119050334
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10001926	0.81[ASN][1000 genomes]
rs10002634	0.93[ASN][1000 genomes]
rs10008013	0.93[ASN][1000 genomes]
rs10014055	0.93[ASN][1000 genomes]
rs10014957	0.93[ASN][1000 genomes]
rs10016206	0.93[ASN][1000 genomes]
rs10016301	0.90[ASN][1000 genomes]
rs10018844	0.93[ASN][1000 genomes]
rs10024837	0.93[ASN][1000 genomes]
rs10025690	0.93[ASN][1000 genomes]
rs10033927	0.93[ASN][1000 genomes]
rs10213280	0.93[ASN][1000 genomes]
rs1028091	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1045817	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11721634	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11723877	0.93[ASN][1000 genomes]
rs11723996	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11726746	0.93[ASN][1000 genomes]
rs11726838	0.93[ASN][1000 genomes]
rs11727684	0.93[ASN][1000 genomes]
rs11727817	0.93[ASN][1000 genomes]
rs11728941	0.93[ASN][1000 genomes]
rs11730327	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11730687	0.93[ASN][1000 genomes]
rs11731179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11734145	0.86[ASN][1000 genomes]
rs11930782	0.93[ASN][1000 genomes]
rs11933280	0.93[ASN][1000 genomes]
rs11934183	0.93[ASN][1000 genomes]
rs11944227	0.93[ASN][1000 genomes]
rs11945329	0.93[ASN][1000 genomes]
rs11945537	0.93[ASN][1000 genomes]
rs11945882	0.93[ASN][1000 genomes]
rs11947244	0.93[ASN][1000 genomes]
rs11947630	0.93[ASN][1000 genomes]
rs13114867	0.90[ASN][1000 genomes]
rs13129847	0.90[ASN][1000 genomes]
rs13435006	0.93[ASN][1000 genomes]
rs1403845	0.93[ASN][1000 genomes]
rs1403846	0.93[ASN][1000 genomes]
rs1523744	0.93[ASN][1000 genomes]
rs1523745	0.93[ASN][1000 genomes]
rs1523746	0.93[ASN][1000 genomes]
rs1589718	0.90[ASN][1000 genomes]
rs17515832	0.93[ASN][1000 genomes]
rs17516430	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17516450	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs17594054	0.93[ASN][1000 genomes]
rs17594243	0.93[ASN][1000 genomes]
rs1996725	0.93[ASN][1000 genomes]
rs2030633	0.93[ASN][1000 genomes]
rs2030634	0.93[ASN][1000 genomes]
rs2204269	0.93[ASN][1000 genomes]
rs2271577	0.93[ASN][1000 genomes]
rs2271578	0.93[ASN][1000 genomes]
rs2272160	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs28396217	0.93[ASN][1000 genomes]
rs28508556	0.93[ASN][1000 genomes]
rs28661939	0.90[CEU][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs34893788	0.82[AMR][1000 genomes]
rs34915366	0.84[AMR][1000 genomes]
rs3817274	0.93[ASN][1000 genomes]
rs4546315	0.93[ASN][1000 genomes]
rs56007507	0.93[ASN][1000 genomes]
rs56258393	0.93[ASN][1000 genomes]
rs56339949	0.93[ASN][1000 genomes]
rs56390335	0.86[ASN][1000 genomes]
rs57605165	0.93[ASN][1000 genomes]
rs58798110	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60858456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61342457	0.93[ASN][1000 genomes]
rs61443542	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62326151	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6534088	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6822996	0.93[ASN][1000 genomes]
rs6842372	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6842689	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6853304	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs6853879	0.90[ASN][1000 genomes]
rs6855052	0.93[ASN][1000 genomes]
rs6855536	0.84[ASN][1000 genomes]
rs6856076	0.93[ASN][1000 genomes]
rs71608347	0.90[ASN][1000 genomes]
rs71608349	0.93[ASN][1000 genomes]
rs72907147	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72907175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909175	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72909186	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72917104	0.93[ASN][1000 genomes]
rs72917146	0.93[ASN][1000 genomes]
rs72917175	0.93[ASN][1000 genomes]
rs72917179	0.93[ASN][1000 genomes]
rs7661522	0.90[ASN][1000 genomes]
rs7685455	0.93[ASN][1000 genomes]
rs9992827	0.90[ASN][1000 genomes]
rs9996753	0.93[ASN][1000 genomes]
rs9996762	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1008236	chr4:118989467-119154024	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999152	chr4:119001143-119138322	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv34038	chr4:119035124-119455391	Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119041600-119053000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:119050200-119052200	ZNF genes & repeats	Dnd41	blood

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