Variant report

Variant	rs7687064
Chromosome Location	chr4:175685503-175685504
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:175684622..175686484-chr4:176046452..176048975,2	MCF-7	breast:
2	chr4:175679569..175681556-chr4:175684065..175686816,2	K562	blood:
3	chr4:175679569..175682349-chr4:175685316..175687885,2	K562	blood:
4	chr4:175285862..175286838-chr4:175684965..175685904,3	K562	blood:
5	chr4:175684995..175685845-chr4:176457861..176458680,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10004000	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.90[MEX][hapmap];0.80[TSI][hapmap]
rs10049967	0.85[CHB][hapmap];1.00[CHD][hapmap]
rs1012342	0.82[CHB][hapmap];1.00[CHD][hapmap];0.90[MEX][hapmap];0.82[ASN][1000 genomes]
rs11727514	0.82[CHB][hapmap]
rs1385843	0.90[CEU][hapmap]
rs1485936	0.95[CEU][hapmap]
rs2029569	0.82[CHB][hapmap]
rs4695789	0.95[CEU][hapmap];0.91[TSI][hapmap]
rs4695958	0.95[CEU][hapmap]
rs4695959	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs6553811	0.95[CEU][hapmap]
rs6553812	0.95[CEU][hapmap]
rs6553814	0.95[CEU][hapmap];0.91[TSI][hapmap]
rs6553826	0.82[ASN][1000 genomes]
rs6838215	1.00[CHB][hapmap];0.86[GIH][hapmap]
rs7657731	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs7665933	0.95[CEU][hapmap];0.91[TSI][hapmap]
rs7685430	0.95[CEU][hapmap];0.88[JPT][hapmap]
rs7693058	0.95[CEU][hapmap];0.88[JPT][hapmap]
rs9992190	0.81[CEU][hapmap];0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1034301	chr4:175656538-176055348	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv537364	chr4:175656538-176055348	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1030235	chr4:175663839-175969742	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv537365	chr4:175663839-175969742	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1027622	chr4:175680329-175716070	Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	2 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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