Variant report

Variant	rs10878484
Chromosome Location	chr12:67038140-67038141
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	chr12:67032690..67034327-chr12:67037087..67039046,2	MCF-7	breast:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10748057	0.86[EUR][1000 genomes]
rs10748058	0.86[EUR][1000 genomes]
rs10748059	0.86[EUR][1000 genomes]
rs10784559	0.86[EUR][1000 genomes]
rs10784561	0.86[EUR][1000 genomes]
rs10784562	0.86[EUR][1000 genomes]
rs10784564	0.86[EUR][1000 genomes]
rs10784565	0.86[EUR][1000 genomes]
rs10784566	0.86[EUR][1000 genomes]
rs10784567	0.86[EUR][1000 genomes]
rs10784568	0.86[EUR][1000 genomes]
rs10784569	0.86[EUR][1000 genomes]
rs10784570	0.84[EUR][1000 genomes]
rs10784571	0.86[EUR][1000 genomes]
rs10878470	0.84[EUR][1000 genomes]
rs10878471	0.84[EUR][1000 genomes]
rs10878472	0.84[EUR][1000 genomes]
rs10878478	0.86[EUR][1000 genomes]
rs10878480	0.86[EUR][1000 genomes]
rs10878481	0.86[EUR][1000 genomes]
rs11176332	0.84[EUR][1000 genomes]
rs11176335	0.84[EUR][1000 genomes]
rs11176336	0.84[EUR][1000 genomes]
rs11176337	0.84[EUR][1000 genomes]
rs11176343	0.86[EUR][1000 genomes]
rs11176344	0.86[EUR][1000 genomes]
rs11176345	0.86[EUR][1000 genomes]
rs11176347	0.86[EUR][1000 genomes]
rs11176349	0.86[EUR][1000 genomes]
rs11176350	0.86[EUR][1000 genomes]
rs11176351	0.86[EUR][1000 genomes]
rs11176352	0.86[EUR][1000 genomes]
rs11176354	0.86[EUR][1000 genomes]
rs11176355	0.86[EUR][1000 genomes]
rs11176356	0.86[EUR][1000 genomes]
rs11615485	0.86[EUR][1000 genomes]
rs12230590	0.84[EUR][1000 genomes]
rs34639740	0.82[EUR][1000 genomes]
rs4290313	0.86[EUR][1000 genomes]
rs4414309	0.86[EUR][1000 genomes]
rs4489824	0.86[EUR][1000 genomes]
rs4587801	0.86[EUR][1000 genomes]
rs57730465	0.86[EUR][1000 genomes]
rs59859388	0.86[EUR][1000 genomes]
rs61926094	0.84[EUR][1000 genomes]
rs61926104	0.85[EUR][1000 genomes]
rs61926113	0.86[EUR][1000 genomes]
rs7301248	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73127190	0.84[EUR][1000 genomes]
rs7485667	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv832449	chr12:66885819-67069953	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv469461	chr12:67007070-67038595	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv559208	chr12:67007070-67038595	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67029200-67040000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:67033800-67038600	Weak transcription	Fetal Kidney	kidney
3	chr12:67035000-67040800	Weak transcription	Fetal Brain Male	brain

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