Variant report

Variant	rs7702105
Chromosome Location	chr5:152283840-152283841
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10056647	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11167604	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12153071	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12153328	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12186623	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12188960	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12654450	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13182323	0.81[ASN][1000 genomes]
rs13187261	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17488630	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17489682	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4310018	0.81[EUR][1000 genomes]
rs4394168	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4437425	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55829928	0.97[EUR][1000 genomes]
rs55992747	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56117655	0.81[ASN][1000 genomes]
rs56269251	0.97[EUR][1000 genomes]
rs6579993	0.81[ASN][1000 genomes]
rs72799185	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72799186	0.94[EUR][1000 genomes]
rs72799196	0.97[EUR][1000 genomes]
rs72799198	0.97[EUR][1000 genomes]
rs72799200	0.97[EUR][1000 genomes]
rs72799201	0.97[EUR][1000 genomes]
rs72799202	0.97[EUR][1000 genomes]
rs72801007	0.97[EUR][1000 genomes]
rs72802852	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72802853	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72802868	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72802874	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72802883	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72804778	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72804786	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72804798	0.81[ASN][1000 genomes]
rs7702551	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023676	chr5:151979253-152925064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv537927	chr5:151979253-152925064	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv883049	chr5:152159184-152399894	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv600089	chr5:152200109-152488891	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1017812	chr5:152220845-152467431	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv537928	chr5:152220845-152467431	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1017488	chr5:152239716-152383640	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1016480	chr5:152261713-152313172	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription	lncRNA	n/a	inside rSNPs	diseases
9	nsv883050	chr5:152277537-152540026	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1019978	chr5:152278020-152316446	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	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	chr5:152282200-152287000	Weak transcription	Liver	Liver

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