Variant report

Variant	rs9394200
Chromosome Location	chr6:34218718-34218719
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34212618..34219497-chr6:34387813..34394246,15	K562	blood:
2	chr6:34213633..34219276-chr6:34358105..34363296,16	MCF-7	breast:
3	chr6:34214133..34219385-chr6:34356600..34362053,16	K562	blood:
4	chr6:34218417..34220144-chr6:34295375..34297652,2	K562	blood:
5	chr6:34215295..34220270-chr6:34358417..34361933,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000124614	Chromatin interaction
ENSG00000272325	Chromatin interaction
ENSG00000270800	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10080749	0.96[ASN][1000 genomes]
rs10807138	0.86[ASN][1000 genomes]
rs1150777	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1150779	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];0.82[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1150781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12530053	0.82[ASN][1000 genomes]
rs1573905	1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1592269	0.86[CHB][hapmap]
rs16885998	1.00[CEU][hapmap]
rs16889706	1.00[CEU][hapmap]
rs16889714	1.00[CEU][hapmap]
rs1759628	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1759645	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1776877	0.88[CHB][hapmap]
rs1776891	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1776897	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap]
rs1776899	0.83[AMR][1000 genomes]
rs2071928	1.00[CEU][hapmap]
rs2483211	0.89[ASN][1000 genomes]
rs2780216	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2780226	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[MEX][hapmap]
rs2797967	0.91[ASN][1000 genomes]
rs28539536	0.81[AMR][1000 genomes]
rs28844869	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3778077	1.00[CEU][hapmap]
rs3798562	1.00[CEU][hapmap]
rs3798564	1.00[CEU][hapmap]
rs3997803	0.81[ASN][1000 genomes]
rs4711389	0.84[AMR][1000 genomes]
rs4711390	1.00[CEU][hapmap]
rs4713761	0.83[AMR][1000 genomes]
rs4713763	0.82[ASN][1000 genomes]
rs4713764	0.81[ASN][1000 genomes]
rs4713765	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4713766	1.00[CEU][hapmap]
rs4713774	1.00[CEU][hapmap]
rs4713784	1.00[CEU][hapmap]
rs56657958	0.86[AMR][1000 genomes]
rs57026767	0.94[ASN][1000 genomes]
rs59412811	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6457769	0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6899897	0.82[ASN][1000 genomes]
rs6900030	0.82[ASN][1000 genomes]
rs6900387	0.80[ASN][1000 genomes]
rs6909732	1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6918981	0.90[CHD][hapmap];0.88[JPT][hapmap]
rs6922699	0.82[ASN][1000 genomes]
rs6922851	0.82[ASN][1000 genomes]
rs6932690	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73419191	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73420913	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7740907	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7742369	0.88[CHB][hapmap];0.95[CHD][hapmap]
rs7753987	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7761883	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7765484	0.82[ASN][1000 genomes]
rs7768482	0.81[ASN][1000 genomes]
rs928482	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9348936	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9366846	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9368805	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9394201	0.94[ASN][1000 genomes]
rs9394202	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9461968	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9461969	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9461975	0.81[ASN][1000 genomes]
rs9469750	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9469757	0.82[ASN][1000 genomes]
rs9469758	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9469761	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs9469762	0.80[EUR][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	nsv885781	chr6:34110257-34247661	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv462903	chr6:34110257-34263743	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv602863	chr6:34110257-34263743	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv885784	chr6:34187206-34246714	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	esv1798756	chr6:34203406-34319041	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	esv1798835	chr6:34204183-34319041	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	esv1840881	chr6:34204285-34231570	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv1792088	chr6:34204285-34318837	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	esv1793127	chr6:34204285-34319041	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv969388	chr6:34213490-34240324	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34217800-34219400	Enhancers	Primary B cells from cord blood	blood
2	chr6:34218000-34219200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr6:34218000-34228000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:34218200-34219800	Weak transcription	Placenta	Placenta
5	chr6:34218200-34220400	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr6:34218200-34222800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:34218200-34230600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:34218200-34255000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr6:34218400-34220000	Weak transcription	K562	blood

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