Variant report

Variant	rs874777
Chromosome Location	chr8:64984947-64984948
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:64982766..64985265-chr8:64985566..64987606,2	MCF-7	breast:
2	chr8:64982200..64985082-chr8:64993821..64995361,2	MCF-7	breast:

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

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

rs_ID	r²[population]
rs10504371	0.89[EUR][1000 genomes]
rs12549556	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12549559	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13255222	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13256546	0.88[EUR][1000 genomes]
rs13271553	0.95[ASN][1000 genomes]
rs13273490	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13280176	0.89[EUR][1000 genomes]
rs1444511	0.99[ASN][1000 genomes]
rs1550730	0.99[ASN][1000 genomes]
rs1838420	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1838421	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1838424	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2018264	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2083995	0.88[EUR][1000 genomes]
rs2099982	0.99[ASN][1000 genomes]
rs2356371	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2883916	0.97[ASN][1000 genomes]
rs35496690	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3910845	0.91[AMR][1000 genomes]
rs4027777	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4147346	0.99[ASN][1000 genomes]
rs4475525	0.90[ASN][1000 genomes]
rs6472131	0.99[ASN][1000 genomes]
rs6981673	0.84[EUR][1000 genomes]
rs6985609	0.95[ASN][1000 genomes]
rs6988220	0.95[ASN][1000 genomes]
rs6991156	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7014553	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7017705	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7844737	0.95[ASN][1000 genomes]
rs920875	0.99[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	nsv948343	chr8:64804219-65328394	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv890969	chr8:64807144-65047353	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv890970	chr8:64975466-65125295	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64982600-64992000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr8:64984600-64985200	Enhancers	HUES48 Cell Line	embryonic stem cell

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