Variant report

Variant	rs10274159
Chromosome Location	chr7:15462199-15462200
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10215934	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10216294	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10224377	0.87[EUR][1000 genomes]
rs10234651	0.87[EUR][1000 genomes]
rs10241564	0.91[EUR][1000 genomes]
rs10267969	0.80[AMR][1000 genomes]
rs10269015	0.87[EUR][1000 genomes]
rs13438427	1.00[ASN][1000 genomes]
rs13438428	1.00[ASN][1000 genomes]
rs28395179	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28410562	1.00[ASN][1000 genomes]
rs28447310	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28459767	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28526445	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28541411	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28546418	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28626386	0.91[EUR][1000 genomes]
rs28635514	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28674724	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28682961	0.86[ASN][1000 genomes]
rs28688256	1.00[ASN][1000 genomes]
rs28754437	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4263651	0.86[ASN][1000 genomes]
rs4263652	0.86[ASN][1000 genomes]
rs4286842	1.00[ASN][1000 genomes]
rs58268106	0.86[ASN][1000 genomes]
rs58852304	0.87[EUR][1000 genomes]
rs59662825	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60157613	0.83[ASN][1000 genomes]
rs60860345	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439269	0.87[EUR][1000 genomes]
rs62439274	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439276	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439280	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439282	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439283	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62439309	0.82[EUR][1000 genomes]
rs73066509	0.86[ASN][1000 genomes]
rs73302375	0.86[ASN][1000 genomes]
rs7805596	1.00[ASN][1000 genomes]
rs7805764	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032569	chr7:14905287-15597069	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1021172	chr7:14944318-15548794	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv538743	chr7:14944318-15548794	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1028314	chr7:15336831-15555412	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1032866	chr7:15336831-15622515	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1033428	chr7:15343210-15554763	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1023086	chr7:15368522-15554763	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv538746	chr7:15368522-15554763	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv606295	chr7:15397449-15547950	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1031116	chr7:15428343-15568587	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1028545	chr7:15440202-15554763	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv538747	chr7:15440202-15554763	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv887728	chr7:15444355-15479473	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv887729	chr7:15444355-15580078	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15455200-15469800	Weak transcription	Aorta	Aorta
2	chr7:15460400-15464000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:15461200-15462600	Strong transcription	Liver	Liver

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