Variant report

Variant	rs9818564
Chromosome Location	chr3:112628205-112628206
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:112622166..112623673-chr3:112626677..112629494,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10934190	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10934192	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10934193	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13326243	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1387024	0.82[CEU][hapmap]
rs1500878	0.97[ASN][1000 genomes]
rs1500879	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1971986	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2087284	0.82[CEU][hapmap];0.86[YRI][hapmap]
rs2101440	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2399436	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2399443	0.84[AFR][1000 genomes]
rs28859668	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28867393	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4234417	1.00[ASW][hapmap];0.89[CEU][hapmap];0.81[LWK][hapmap];0.90[MEX][hapmap];0.84[MKK][hapmap];0.89[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4478054	0.91[ASN][1000 genomes]
rs4571210	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4682120	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4682440	0.81[AFR][1000 genomes]
rs4682441	0.82[CEU][hapmap]
rs4682444	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6438111	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6438112	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6438113	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6438114	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6438120	0.81[MKK][hapmap]
rs6765367	0.83[EUR][1000 genomes]
rs6765379	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6766388	0.84[AFR][1000 genomes]
rs6791158	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6791672	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7615572	0.81[ASW][hapmap];0.80[TSI][hapmap]
rs7632218	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7646849	0.81[MKK][hapmap]
rs7652536	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9838082	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9847365	0.82[CEU][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes]
rs9868839	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9871985	0.80[TSI][hapmap]
rs9875551	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9879005	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs9879149	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs9883255	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	esv3501334	chr3:112546820-112648766	Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv3501335	chr3:112546820-112648766	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv1843165	chr3:112628205-112740145	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr3:112625200-112629000	Enhancers	Primary B cells from peripheral blood	blood
2	chr3:112627800-112629200	Enhancers	Primary B cells from cord blood	blood
3	chr3:112628000-112634800	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr3:112628000-112634800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr3:112628000-112635200	Weak transcription	Primary T cells from cord blood	blood
6	chr3:112628000-112641800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:112628000-112642000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:112628000-112642000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr3:112628200-112628400	Enhancers	GM12878-XiMat	blood

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