Variant report

Variant	rs4695791
Chromosome Location	chr4:175723697-175723698
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:175722667..175724604-chr4:175731422..175734130,2	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10000099	0.82[ASN][1000 genomes]
rs10014645	0.82[ASN][1000 genomes]
rs10014996	0.82[ASN][1000 genomes]
rs10017956	0.95[CEU][hapmap];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10018097	1.00[ASN][1000 genomes]
rs10026240	1.00[ASN][1000 genomes]
rs11133056	1.00[CEU][hapmap]
rs11730303	1.00[ASN][1000 genomes]
rs11934209	0.93[YRI][hapmap]
rs13104813	0.82[ASN][1000 genomes]
rs13105754	0.95[CEU][hapmap]
rs13106865	0.82[ASN][1000 genomes]
rs13114290	1.00[ASN][1000 genomes]
rs13122361	1.00[ASN][1000 genomes]
rs13435245	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13435599	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1844825	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1994701	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs28496931	1.00[ASN][1000 genomes]
rs28684841	1.00[ASN][1000 genomes]
rs35865475	0.82[ASN][1000 genomes]
rs62332437	1.00[ASN][1000 genomes]
rs62332438	1.00[ASN][1000 genomes]
rs62332439	1.00[ASN][1000 genomes]
rs6811855	0.82[ASN][1000 genomes]
rs6812024	0.82[ASN][1000 genomes]
rs7437746	1.00[ASN][1000 genomes]
rs7668755	1.00[ASN][1000 genomes]

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	esv3416499	chr4:175700801-175744305	Enhancers Weak transcription	Chromatin interactive region	n/a	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
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