Variant report

Variant	rs6097967
Chromosome Location	chr20:53027352-53027353
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:53026253..53028850-chr20:53030160..53033071,3	MCF-7	breast:
2	chr20:53024747..53028563-chr20:53034818..53037384,3	MCF-7	breast:
3	chr20:53026209..53029176-chr20:53030755..53032487,3	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1007393	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1014808	0.91[ASN][1000 genomes]
rs1321464	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1321465	0.86[ASN][1000 genomes]
rs1321468	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1358806	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1358807	0.99[ASN][1000 genomes]
rs1407043	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1539515	0.80[EUR][1000 genomes]
rs1590206	1.00[ASN][1000 genomes]
rs16999560	0.81[EUR][1000 genomes]
rs16999597	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1841860	0.83[ASN][1000 genomes]
rs1923118	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2126676	0.85[ASN][1000 genomes]
rs2126677	0.81[EUR][1000 genomes]
rs2870329	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55865213	0.81[EUR][1000 genomes]
rs56339826	0.81[EUR][1000 genomes]
rs56881371	0.80[ASN][1000 genomes]
rs6013997	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6013999	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6014003	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6014004	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6014005	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6014011	0.85[ASN][1000 genomes]
rs6014013	0.85[ASN][1000 genomes]
rs6023153	0.80[ASN][1000 genomes]
rs6023154	0.80[ASN][1000 genomes]
rs6023155	0.81[ASN][1000 genomes]
rs6023156	0.81[ASN][1000 genomes]
rs6023158	0.81[ASN][1000 genomes]
rs6023178	0.92[ASN][1000 genomes]
rs6023179	0.92[ASN][1000 genomes]
rs6023180	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6023181	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6023183	0.97[ASN][1000 genomes]
rs6023185	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6023189	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6023192	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6023193	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6023197	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6023203	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6023227	0.86[ASN][1000 genomes]
rs6091856	0.84[ASN][1000 genomes]
rs6091858	0.80[EUR][1000 genomes]
rs6091860	0.81[EUR][1000 genomes]
rs6097939	0.81[ASN][1000 genomes]
rs6097942	0.80[EUR][1000 genomes]
rs6097943	0.80[EUR][1000 genomes]
rs6097950	0.81[EUR][1000 genomes]
rs6097955	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6097957	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6097963	0.92[ASN][1000 genomes]
rs6097964	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73143321	0.81[EUR][1000 genomes]
rs73143323	0.81[EUR][1000 genomes]
rs73145242	0.81[EUR][1000 genomes]
rs73145250	0.81[EUR][1000 genomes]
rs73145257	0.81[EUR][1000 genomes]
rs73145263	0.81[EUR][1000 genomes]
rs73145273	0.81[EUR][1000 genomes]
rs73145277	0.81[EUR][1000 genomes]
rs793033	0.83[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	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv834011	chr20:52858341-53086042	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv834012	chr20:52921007-53097177	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 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	chr20:53027000-53031400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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