Variant report

Variant	rs34713378
Chromosome Location	chr6:54697569-54697570
allele	-/AT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:54695865..54698667-chr6:54699652..54702495,2	MCF-7	breast:
2	chr6:54688351..54691007-chr6:54693141..54697889,4	MCF-7	breast:
3	chr6:54696307..54700316-chr6:54709756..54713142,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168143	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10223849	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10807484	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10807485	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10948860	0.89[AMR][1000 genomes]
rs10948862	0.83[ASN][1000 genomes]
rs10948864	0.84[ASN][1000 genomes]
rs12191299	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12191386	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12194667	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12195438	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12196314	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12199827	0.84[EUR][1000 genomes]
rs12201892	0.92[ASN][1000 genomes]
rs12202062	0.92[ASN][1000 genomes]
rs12203709	0.85[ASN][1000 genomes]
rs12205372	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12207559	0.84[ASN][1000 genomes]
rs12216039	0.84[ASN][1000 genomes]
rs12216049	0.84[ASN][1000 genomes]
rs1393778	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1393779	0.80[EUR][1000 genomes]
rs1910357	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2270989	0.85[ASN][1000 genomes]
rs4712075	0.85[ASN][1000 genomes]
rs58988305	0.85[EUR][1000 genomes]
rs62412605	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6908745	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72957572	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7747352	0.84[ASN][1000 genomes]
rs7760490	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9296769	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9464138	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9464148	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9464149	0.84[ASN][1000 genomes]
rs9474997	0.84[EUR][1000 genomes]
rs9475005	0.85[EUR][1000 genomes]
rs9475021	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9475029	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9475032	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9475038	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9475039	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9475040	0.85[ASN][1000 genomes]
rs9475041	0.84[ASN][1000 genomes]
rs9475046	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885900	chr6:54517968-54852462	Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2763553	chr6:54687979-54820487	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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