Variant report

Variant	rs10514534
Chromosome Location	chr16:82221607-82221608
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:82207842..82210813-chr16:82220344..82222897,2	MCF-7	breast:
2	chr16:82215365..82217939-chr16:82221171..82222891,2	MCF-7	breast:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10514531	0.84[CEU][hapmap]
rs10514533	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs1056629	0.82[CEU][hapmap]
rs1056654	0.81[CEU][hapmap]
rs1056690	0.82[CEU][hapmap]
rs11150443	0.82[CEU][hapmap]
rs11642247	0.83[CEU][hapmap]
rs11642251	1.00[CEU][hapmap]
rs11643324	0.82[CEU][hapmap]
rs11643724	0.83[CEU][hapmap]
rs11646480	0.92[CEU][hapmap]
rs11647563	0.82[CEU][hapmap]
rs11647691	0.82[CEU][hapmap]
rs11649427	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs12444846	0.82[CEU][hapmap]
rs12445764	0.91[CEU][hapmap]
rs12447225	0.92[CEU][hapmap]
rs12447597	0.83[CEU][hapmap]
rs12448672	0.82[CEU][hapmap]
rs13330853	0.82[CEU][hapmap]
rs1364288	0.82[AMR][1000 genomes]
rs1424153	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956483	0.82[CEU][hapmap]
rs16956556	0.84[CEU][hapmap]
rs16956565	0.84[CEU][hapmap]
rs16956572	0.84[CEU][hapmap]
rs16956576	0.82[CEU][hapmap]
rs16956683	0.81[AMR][1000 genomes]
rs1862821	0.84[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap]
rs2081256	0.82[CEU][hapmap]
rs2081257	0.82[CEU][hapmap]
rs2098749	0.82[CEU][hapmap]
rs2098750	0.84[CEU][hapmap]
rs2303268	0.82[CEU][hapmap]
rs2911428	0.82[CEU][hapmap];0.86[EUR][1000 genomes]
rs34629110	0.82[AMR][1000 genomes]
rs34652971	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3794705	0.92[CEU][hapmap]
rs3829542	0.82[CEU][hapmap]
rs3829552	0.82[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4243231	0.84[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4516225	0.82[AMR][1000 genomes]
rs4530129	0.82[CEU][hapmap]
rs4569272	0.84[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4889478	0.86[EUR][1000 genomes]
rs4889480	0.87[EUR][1000 genomes]
rs57676882	0.82[AMR][1000 genomes]
rs61702998	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7186965	0.84[CEU][hapmap]
rs7192520	0.82[AMR][1000 genomes]
rs7405214	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8049396	0.83[AMR][1000 genomes]
rs9635584	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9635585	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv525467	chr16:82154619-82223485	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv518129	chr16:82188173-82228076	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv833302	chr16:82188351-82363863	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv1844598	chr16:82195234-82429790	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	esv1847414	chr16:82195234-82429790	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv532600	chr16:82197554-82314289	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv907015	chr16:82203758-82284056	Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv1065896	chr16:82213517-82731994	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82219200-82223000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr16:82219400-82223000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr16:82221000-82222000	Enhancers	GM12878-XiMat	blood
4	chr16:82221200-82222200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr16:82221600-82222000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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