Variant report

Variant	rs7564964
Chromosome Location	chr2:56197200-56197201
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10185077	0.99[ASN][1000 genomes]
rs10192259	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11125611	0.94[ASN][1000 genomes]
rs11685113	0.80[EUR][1000 genomes]
rs12472832	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13431149	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1432560	0.98[ASN][1000 genomes]
rs1432561	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1432563	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1432564	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1465685	0.98[ASN][1000 genomes]
rs1583266	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1583267	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1897478	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2278366	0.98[ASN][1000 genomes]
rs2868984	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34552760	0.97[ASN][1000 genomes]
rs3972318	0.97[ASN][1000 genomes]
rs4258837	0.92[CHB][hapmap]
rs4453721	0.96[ASN][1000 genomes]
rs4635565	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4672080	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4672081	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4672082	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55805406	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6545531	0.97[ASN][1000 genomes]
rs6704991	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6721145	0.80[ASN][1000 genomes]
rs6724998	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6733881	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6733889	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6747490	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs724539	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs724540	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7422809	0.91[ASN][1000 genomes]
rs7561395	0.97[ASN][1000 genomes]
rs7561417	0.97[ASN][1000 genomes]
rs981037	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][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	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv874161	chr2:56154316-56203798	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2757799	chr2:56178439-56472394	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
4	esv2759051	chr2:56178439-56472394	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56193400-56202400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:56194000-56197800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:56194000-56216200	Weak transcription	Pancreas	Pancrea
4	chr2:56195800-56198400	Enhancers	NHDF-Ad	bronchial
5	chr2:56195800-56208600	Weak transcription	HUVEC	blood vessel
6	chr2:56197000-56198600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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