Variant report

Variant	rs7760490
Chromosome Location	chr6:54697196-54697197
allele	C/T
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: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10223546	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10456688	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10807484	0.86[ASN][1000 genomes]
rs10807485	0.86[ASN][1000 genomes]
rs10948852	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10948853	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10948862	0.84[ASN][1000 genomes]
rs10948864	0.87[ASN][1000 genomes]
rs12191299	0.86[ASN][1000 genomes]
rs12191386	0.86[ASN][1000 genomes]
rs12194667	0.86[ASN][1000 genomes]
rs12195438	0.83[ASN][1000 genomes]
rs12196314	0.96[ASN][1000 genomes]
rs12201892	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12202062	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12203709	0.86[ASN][1000 genomes]
rs12205222	0.80[ASN][1000 genomes]
rs12205372	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12207559	0.85[ASN][1000 genomes]
rs12216039	0.85[ASN][1000 genomes]
rs12216049	0.85[ASN][1000 genomes]
rs12216186	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13195757	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1567164	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1827513	0.81[EUR][1000 genomes]
rs1910357	0.86[ASN][1000 genomes]
rs2270989	0.86[ASN][1000 genomes]
rs34713378	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4712071	0.82[ASN][1000 genomes]
rs4712075	0.86[ASN][1000 genomes]
rs4715480	0.88[EUR][1000 genomes]
rs4715481	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4715482	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4715484	0.93[EUR][1000 genomes]
rs62412605	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6908745	0.86[ASN][1000 genomes]
rs6908940	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6918226	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6922162	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6922543	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6939992	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72957572	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7452200	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7747352	0.87[ASN][1000 genomes]
rs9296768	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9296769	0.86[ASN][1000 genomes]
rs9464138	0.81[ASN][1000 genomes]
rs9464139	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9464148	0.87[ASN][1000 genomes]
rs9464149	0.87[ASN][1000 genomes]
rs9475004	0.80[EUR][1000 genomes]
rs9475006	0.88[EUR][1000 genomes]
rs9475011	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9475013	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9475017	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9475021	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9475029	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9475038	0.87[ASN][1000 genomes]
rs9475039	0.86[ASN][1000 genomes]
rs9475040	0.86[ASN][1000 genomes]
rs9475041	0.87[ASN][1000 genomes]
rs9475045	0.82[ASN][1000 genomes]
rs9475046	0.87[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
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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