Variant report

Variant	rs10034473
Chromosome Location	chr4:118297556-118297557
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10005949	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10012436	1.00[ASN][1000 genomes]
rs10027838	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10028318	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10471009	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13103240	0.87[ASN][1000 genomes]
rs13119124	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13129266	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13137263	1.00[CHB][hapmap]
rs13138792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17861816	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17865009	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17865320	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17865878	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17866198	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867182	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867290	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17867291	0.87[ASN][1000 genomes]
rs17869432	1.00[CEU][hapmap]
rs28610484	1.00[ASN][1000 genomes]
rs4834611	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4834613	0.87[ASN][1000 genomes]
rs6852103	0.87[ASN][1000 genomes]
rs9307435	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004858	chr4:118248984-118382051	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv427692	chr4:118262899-118437573	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv879825	chr4:118292314-118333367	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
4	nsv879826	chr4:118292314-118351381	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv470068	chr4:118296960-118327792	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118282000-118302000	Weak transcription	HMEC	breast
2	chr4:118295800-118306200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:118297400-118297800	Enhancers	Fetal Brain Male	brain

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