Variant report

Variant	rs13147736
Chromosome Location	chr4:69020429-69020430
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 115 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10004522	1.00[CEU][hapmap];0.86[JPT][hapmap];0.88[EUR][1000 genomes]
rs10018943	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10021559	0.84[EUR][1000 genomes]
rs1079449	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11131733	0.80[EUR][1000 genomes]
rs11131735	0.86[EUR][1000 genomes]
rs11131737	0.86[JPT][hapmap]
rs11131739	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11727567	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11731769	1.00[CEU][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11733984	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11940802	0.86[EUR][1000 genomes]
rs11947862	0.92[EUR][1000 genomes]
rs11947869	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12501405	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12501540	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12502214	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12502757	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12502946	1.00[CEU][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12503814	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12503983	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs12504120	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12504557	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12506837	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12507309	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12507767	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12645384	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12648112	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12651598	0.86[EUR][1000 genomes]
rs13115003	1.00[CEU][hapmap]
rs13132100	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13132990	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13135438	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13138038	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs13148584	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1320264	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13435884	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1370828	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs1370830	1.00[CEU][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes]
rs1370832	1.00[CEU][hapmap]
rs1438389	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438439	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438440	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438441	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438442	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438443	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438444	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438445	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1438447	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1530062	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1530063	0.95[CEU][hapmap];0.84[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17089005	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17089042	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs1837215	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1866327	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1866328	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1866329	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1898644	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1946827	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs2028249	0.80[EUR][1000 genomes]
rs2118625	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2164935	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2319793	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2319798	0.80[ASN][1000 genomes]
rs28535832	0.80[EUR][1000 genomes]
rs34237875	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3819257	1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4317250	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4374659	1.00[CEU][hapmap];0.92[JPT][hapmap]
rs4407557	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4538543	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4613616	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4640716	0.80[EUR][1000 genomes]
rs4860273	0.92[CEU][hapmap];0.86[JPT][hapmap]
rs4860274	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs4860275	0.95[CEU][hapmap];0.86[JPT][hapmap]
rs4860276	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4860277	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4860278	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4860282	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4860875	0.80[EUR][1000 genomes]
rs4860897	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4860908	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59649794	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6552134	0.86[CEU][hapmap]
rs6552145	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes]
rs66943336	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6811052	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs6812743	0.91[EUR][1000 genomes]
rs6819568	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6827417	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6842578	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71604558	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7435855	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7664796	0.80[EUR][1000 genomes]
rs7665583	0.80[EUR][1000 genomes]
rs7674140	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7688501	0.80[EUR][1000 genomes]
rs7688721	0.80[EUR][1000 genomes]
rs939206	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs966827	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs9999589	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879219	chr4:68743032-69028913	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2759257	chr4:68777006-69028913	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv1814820	chr4:68789778-69033099	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv1805370	chr4:68789778-69043722	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	esv2757060	chr4:68790864-69028913	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	esv1812856	chr4:68791333-69021023	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv1008084	chr4:68797598-69482831	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
8	nsv537131	chr4:68797598-69482831	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv879221	chr4:68915798-69033099	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	esv1812438	chr4:68943858-69154222	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	esv1806586	chr4:68943858-69592846	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
12	nsv879222	chr4:68958980-69022380	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	esv3400302	chr4:69008235-69034717	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13147736	GCOM2	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69014800-69028000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:69020400-69020600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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