Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13435481	0.89[EUR][1000 genomes]
rs4383633	0.89[EUR][1000 genomes]
rs4593148	0.89[EUR][1000 genomes]
rs57504424	0.89[EUR][1000 genomes]
rs57633949	0.89[EUR][1000 genomes]
rs60074415	0.89[EUR][1000 genomes]
rs60120540	0.89[EUR][1000 genomes]
rs61471044	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72615878	0.89[EUR][1000 genomes]
rs72615884	0.89[EUR][1000 genomes]
rs72615885	0.89[EUR][1000 genomes]
rs72615886	0.89[EUR][1000 genomes]
rs72615895	0.89[EUR][1000 genomes]
rs72616304	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72616305	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616306	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616307	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616359	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72616370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72616381	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72616382	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72616384	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv1017270	chr4:130853337-130982586	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv3373209	chr4:130931327-130933875	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
4	esv3348628	chr4:130931552-130933650	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130932600-130945000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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