Variant report

Variant	rs73776225
Chromosome Location	chr5:97241733-97241734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11135533	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11135534	0.90[ASN][1000 genomes]
rs11135535	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11135536	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11135546	0.90[ASN][1000 genomes]
rs11739685	0.90[ASN][1000 genomes]
rs11741372	0.90[ASN][1000 genomes]
rs11742020	0.90[ASN][1000 genomes]
rs11742033	0.90[ASN][1000 genomes]
rs11742228	0.90[ASN][1000 genomes]
rs11948604	0.90[ASN][1000 genomes]
rs11951691	0.84[ASN][1000 genomes]
rs11951743	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11952012	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11952804	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11953565	0.90[ASN][1000 genomes]
rs11954953	0.90[ASN][1000 genomes]
rs11955639	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11955806	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11955809	0.90[ASN][1000 genomes]
rs11957127	0.90[ASN][1000 genomes]
rs11957285	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11958382	0.90[AMR][1000 genomes]
rs11958448	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11959461	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11960597	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12652203	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12652224	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12655656	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17087911	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34471407	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35576919	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4377726	0.90[ASN][1000 genomes]
rs4461658	0.90[ASN][1000 genomes]
rs4518427	0.90[ASN][1000 genomes]
rs59069286	0.90[ASN][1000 genomes]
rs6557014	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6557015	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73154946	0.90[ASN][1000 genomes]
rs73154947	0.90[ASN][1000 genomes]
rs73154954	0.90[ASN][1000 genomes]
rs73154956	0.90[ASN][1000 genomes]
rs73154957	0.90[ASN][1000 genomes]
rs73154962	0.90[ASN][1000 genomes]
rs73154963	0.90[ASN][1000 genomes]
rs73154965	0.90[ASN][1000 genomes]
rs73154987	0.90[ASN][1000 genomes]
rs73154988	0.90[ASN][1000 genomes]
rs73154995	0.90[ASN][1000 genomes]
rs73154998	0.90[ASN][1000 genomes]
rs73156003	0.90[ASN][1000 genomes]
rs73156004	0.90[ASN][1000 genomes]
rs7703831	0.90[ASN][1000 genomes]
rs7715192	0.90[ASN][1000 genomes]
rs7715212	0.90[ASN][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	nsv534326	chr5:96531217-97283481	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1031429	chr5:96777286-97269498	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv527650	chr5:96783726-97260358	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1028224	chr5:96791214-97258383	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv537814	chr5:96791214-97258383	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1020125	chr5:96937248-97350644	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv2754965	chr5:97013452-97296147	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv830418	chr5:97139371-97326878	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3372859	chr5:97190949-97325577	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1016231	chr5:97206242-97420435	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97240800-97245200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:97241400-97243400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr5:97241600-97241800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:97241600-97241800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr5:97241600-97242400	Enhancers	Stomach Mucosa	stomach
6	chr5:97241600-97242600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr5:97241600-97243200	Enhancers	HUES64 Cell Line	embryonic stem cell

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