Variant report

Variant	rs7639707
Chromosome Location	chr3:159148087-159148088
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:159147245..159149720-chr3:159151129..159153409,4	MCF-7	breast:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11917829	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830135	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs16830184	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830232	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16830267	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs16830290	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs16830298	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16830299	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16830314	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16830326	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs16830331	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16830334	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1844468	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1973660	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2029100	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2029101	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2102724	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3912726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6796565	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7620323	1.00[YRI][hapmap]
rs7620403	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7629397	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7631740	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7642306	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9871361	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1004990	chr3:159090974-159174954	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:159147800-159149000	Weak transcription	Fetal Brain Male	brain

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