Variant report

Variant	rs4715469
Chromosome Location	chr6:54561417-54561418
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:54558970..54566519-chr6:54708534..54713743,16	MCF-7	breast:
2	chr6:54560120..54562700-chr6:54564068..54565878,2	MCF-7	breast:
3	chr6:54559522..54567174-chr6:54707552..54714330,37	MCF-7	breast:
4	chr6:54560857..54562671-chr6:54739251..54742148,2	MCF-7	breast:
5	chr6:54560989..54563870-chr6:54779771..54781666,2	MCF-7	breast:
6	chr6:54561293..54570100-chr6:54582505..54590247,14	MCF-7	breast:
7	chr6:54559803..54567776-chr6:54579525..54585377,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168143	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1018141	0.88[EUR][1000 genomes]
rs10948842	0.88[EUR][1000 genomes]
rs11967781	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11967833	1.00[CEU][hapmap];0.87[CHB][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12198936	1.00[CEU][hapmap];0.87[CHB][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12208090	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12211545	0.83[EUR][1000 genomes]
rs12527497	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12529276	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1395632	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1395635	1.00[CEU][hapmap];0.87[CHB][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1948954	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1983140	0.91[CHB][hapmap]
rs2089411	0.89[EUR][1000 genomes]
rs34970714	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4712070	0.87[JPT][hapmap]
rs540890	0.86[EUR][1000 genomes]
rs6903280	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6906715	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7746312	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7753256	0.88[EUR][1000 genomes]
rs9296764	0.92[CEU][hapmap];0.87[CHB][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

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

No data

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