Variant report

Variant	rs72615864
Chromosome Location	chr4:130781766-130781767
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11931514	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11940610	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12648472	0.84[EUR][1000 genomes]
rs2391539	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs28698400	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28727307	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4383633	1.00[AFR][1000 genomes]
rs4512011	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57504424	1.00[AFR][1000 genomes]
rs57633949	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs59382846	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs60074415	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs60120540	1.00[AFR][1000 genomes]
rs60882021	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72615856	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72615857	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72615858	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72615859	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72615861	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72615865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72615878	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs72615884	1.00[AFR][1000 genomes]
rs72615885	1.00[AFR][1000 genomes]
rs72615886	1.00[AFR][1000 genomes]
rs72615895	1.00[AFR][1000 genomes]
rs72616304	1.00[AFR][1000 genomes]
rs72616306	1.00[AFR][1000 genomes]
rs72616307	1.00[AFR][1000 genomes]
rs72618851	0.84[EUR][1000 genomes]
rs72618852	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72618853	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7685810	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv428770	chr4:130692631-130863832	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1023482	chr4:130737503-130783577	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1019516	chr4:130754819-130976202	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130781600-130781800	Enhancers	HUES48 Cell Line	embryonic stem cell

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