Variant report

Variant	rs4765855
Chromosome Location	chr12:1997181-1997182
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	chr12:1976877..1978383-chr12:1995618..1998420,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11829061	1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs11838338	1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs12300820	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4765854	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4765856	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58041839	0.86[EUR][1000 genomes]
rs60708075	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60945277	0.86[EUR][1000 genomes]
rs61085710	0.86[EUR][1000 genomes]
rs61386831	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61457024	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7297190	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs73032415	0.92[EUR][1000 genomes]
rs73032423	0.82[EUR][1000 genomes]
rs73032427	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73032431	0.82[EUR][1000 genomes]
rs73032438	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73032440	0.97[EUR][1000 genomes]
rs73032452	0.97[EUR][1000 genomes]
rs73036228	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73036240	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038172	0.92[EUR][1000 genomes]
rs73038195	0.88[EUR][1000 genomes]
rs7308134	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs737102	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs758160	0.80[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7957635	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs7964656	0.87[EUR][1000 genomes]
rs7966806	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7969511	0.93[EUR][1000 genomes]
rs9669070	0.88[CEU][hapmap];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948480	chr12:1776217-2284333	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv832306	chr12:1847726-2001308	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv898598	chr12:1939252-2215448	Strong transcription Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1046388	chr12:1964846-2034887	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1043329	chr12:1986238-2034887	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	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	chr12:1997000-1997400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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