Variant report

Variant	rs10271355
Chromosome Location	chr7:119261782-119261783
allele	A/C
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:40)

rs_ID	r²[population]
rs10245797	0.81[ASN][1000 genomes]
rs10246845	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10258423	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10267600	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10267793	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10274141	0.81[ASN][1000 genomes]
rs10275167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10279364	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11767407	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11770085	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12537312	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12540739	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28843793	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28893249	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4132827	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4341091	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4486113	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4518596	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4617096	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727897	0.81[ASN][1000 genomes]
rs4727901	0.81[ASN][1000 genomes]
rs4730924	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4730930	0.81[ASN][1000 genomes]
rs4730933	0.81[ASN][1000 genomes]
rs5009239	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58141692	0.81[ASN][1000 genomes]
rs6466708	0.81[ASN][1000 genomes]
rs6955486	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6958096	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73483305	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73483374	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73720503	0.81[ASN][1000 genomes]
rs73722420	0.81[ASN][1000 genomes]
rs73722422	0.81[ASN][1000 genomes]
rs73722423	0.81[ASN][1000 genomes]
rs7782632	0.81[ASN][1000 genomes]
rs7796017	0.81[ASN][1000 genomes]
rs7799128	0.81[ASN][1000 genomes]
rs7799153	0.81[ASN][1000 genomes]
rs7799166	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949327	chr7:119179990-119402882	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv889114	chr7:119206096-119440159	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1020551	chr7:119232910-119292763	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119259800-119262000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:119260800-119261800	Enhancers	HUES64 Cell Line	embryonic stem cell

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