Variant report

Variant	rs1014584
Chromosome Location	chr2:37017526-37017527
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10171853	1.00[ASN][1000 genomes]
rs10174832	1.00[ASN][1000 genomes]
rs10177789	1.00[ASN][1000 genomes]
rs10177905	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10179017	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10180537	0.80[AMR][1000 genomes]
rs10209055	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10209211	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11124543	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11124545	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11692052	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464180	1.00[CHD][hapmap]
rs12618630	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12987048	0.89[MEX][hapmap]
rs13382481	1.00[ASN][1000 genomes]
rs13385947	1.00[ASN][1000 genomes]
rs13394344	1.00[ASN][1000 genomes]
rs13398292	1.00[ASN][1000 genomes]
rs13398577	1.00[ASN][1000 genomes]
rs13398883	1.00[ASN][1000 genomes]
rs13411242	1.00[ASN][1000 genomes]
rs13419229	1.00[ASN][1000 genomes]
rs13423835	1.00[ASN][1000 genomes]
rs13429524	1.00[ASN][1000 genomes]
rs1558701	0.81[CEU][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap]
rs2247010	1.00[CHD][hapmap]
rs2372713	0.91[CEU][hapmap];0.97[GIH][hapmap];0.82[MEX][hapmap];0.97[TSI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2540923	1.00[CHD][hapmap]
rs2691111	1.00[CHD][hapmap]
rs28692629	1.00[ASN][1000 genomes]
rs34040386	0.82[AMR][1000 genomes]
rs4670171	0.82[CEU][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4670610	1.00[ASN][1000 genomes]
rs4670618	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56808546	1.00[ASN][1000 genomes]
rs6544039	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6716891	1.00[CHD][hapmap]
rs6721362	0.94[CEU][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7572592	1.00[ASN][1000 genomes]
rs7606098	0.86[CEU][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs763724	0.81[CEU][hapmap]
rs9308999	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv428395	chr2:36990348-37300352	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	esv1821275	chr2:36991736-37018278	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv2682	chr2:37015550-37060432	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37010000-37021600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr2:37012800-37024800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:37013000-37033000	Weak transcription	Ovary	ovary
4	chr2:37013200-37024400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:37016200-37018600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:37016200-37019600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:37016800-37020200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr2:37016800-37024600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr2:37017000-37018400	Weak transcription	Thymus	Thymus
10	chr2:37017200-37018400	Weak transcription	Fetal Thymus	thymus

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