Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:79156655..79159520-chr8:79164294..79166738,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs13253307	0.85[ASN][1000 genomes]
rs13254490	0.90[AMR][1000 genomes]
rs13254799	0.90[AMR][1000 genomes]
rs13265230	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13266447	0.89[AFR][1000 genomes]
rs13266679	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13274740	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17486452	0.85[ASN][1000 genomes]
rs1820997	0.93[AMR][1000 genomes]
rs2369095	0.86[AMR][1000 genomes]
rs2369096	0.90[AMR][1000 genomes]
rs34064734	0.90[AMR][1000 genomes]
rs34219583	0.90[AMR][1000 genomes]
rs34294037	0.90[AMR][1000 genomes]
rs34447318	0.93[AMR][1000 genomes]
rs34491063	0.90[AMR][1000 genomes]
rs34500915	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34678843	0.90[AMR][1000 genomes]
rs34944617	0.85[ASN][1000 genomes]
rs34963073	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35208372	0.93[AMR][1000 genomes]
rs35245347	0.90[AMR][1000 genomes]
rs35316312	0.90[AMR][1000 genomes]
rs35334031	0.90[AMR][1000 genomes]
rs35579758	0.86[AMR][1000 genomes]
rs35711420	0.90[AMR][1000 genomes]
rs36002580	0.89[AFR][1000 genomes]
rs36055647	0.93[AMR][1000 genomes]
rs4551342	0.90[AMR][1000 genomes]
rs59801513	0.85[ASN][1000 genomes]
rs62510296	0.89[AFR][1000 genomes]
rs62517358	0.90[AMR][1000 genomes]
rs6988476	0.90[AMR][1000 genomes]
rs71500592	0.84[AMR][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	nsv831364	chr8:79034769-79223319	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv891055	chr8:79110386-79256864	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv831365	chr8:79128833-79281645	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv6266	chr8:79156823-79202020	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 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	chr8:79165800-79173200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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