Variant report

Variant	rs57737362
Chromosome Location	chr7:65490612-65490613
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs2279903	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3735144	0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4149458	0.83[AMR][1000 genomes]
rs4149459	0.83[AMR][1000 genomes]
rs58600265	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58976916	1.00[AMR][1000 genomes]
rs59697660	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60220916	1.00[AMR][1000 genomes]
rs60748223	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61240358	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61665304	0.92[AMR][1000 genomes]
rs73368796	1.00[AMR][1000 genomes]
rs73370623	0.92[AMR][1000 genomes]
rs73370679	0.92[AMR][1000 genomes]
rs73370687	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73372603	1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs73372614	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73372618	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73372623	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73372662	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73372665	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73372688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73372692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73372693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9638231	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9638481	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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	125 gene(s)	inside rSNPs	diseases
3	nsv1025494	chr7:65402301-65515606	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv538906	chr7:65402301-65515606	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv888325	chr7:65474919-65575893	Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv3370332	chr7:65489217-65491915	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3445852	chr7:65489667-65491765	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3477305	chr7:65490212-65490890	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3507641	chr7:65490243-65490901	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3507644	chr7:65490257-65490861	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3477304	chr7:65490261-65490865	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3387893	chr7:65490277-65490864	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3507645	chr7:65490293-65490826	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3477306	chr7:65490338-65490783	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3507643	chr7:65490347-65490785	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3477307	chr7:65490352-65490780	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3507646	chr7:65490352-65490780	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65489000-65497400	Weak transcription	Liver	Liver

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