Variant report

Variant	rs1828383
Chromosome Location	chr9:15525054-15525055
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:15512114..15513693-chr9:15523609..15526046,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10124624	0.96[ASN][1000 genomes]
rs10283923	0.86[CEU][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10283927	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1046388	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10962048	1.00[JPT][hapmap]
rs12336503	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12336509	0.93[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12339417	0.92[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12380487	0.82[CHB][hapmap]
rs12685082	1.00[JPT][hapmap]
rs13248	0.89[JPT][hapmap]
rs16933311	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs16933316	0.89[JPT][hapmap]
rs16933320	0.89[JPT][hapmap]
rs16933348	0.83[ASN][1000 genomes]
rs2175257	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2457637	0.81[AFR][1000 genomes]
rs2777949	0.86[CEU][hapmap]
rs2777950	0.84[CEU][hapmap];0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs28515581	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28537229	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4557796	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56361298	0.83[ASN][1000 genomes]
rs57467578	0.83[ASN][1000 genomes]
rs58607272	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62571010	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62571022	0.83[ASN][1000 genomes]
rs62571023	0.83[ASN][1000 genomes]
rs62571024	0.83[ASN][1000 genomes]
rs62571027	0.88[ASN][1000 genomes]
rs62571030	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62571031	0.96[ASN][1000 genomes]
rs62571032	0.96[ASN][1000 genomes]
rs6474927	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7018658	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7021153	0.83[AFR][1000 genomes]
rs73408328	0.83[ASN][1000 genomes]
rs73644657	0.94[ASN][1000 genomes]
rs7852774	0.96[ASN][1000 genomes]
rs7856318	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs7856710	0.96[ASN][1000 genomes]
rs7857933	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7862428	0.86[CEU][hapmap];0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7863046	0.89[JPT][hapmap]
rs7863139	0.81[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	nsv517975	chr9:15286446-15534070	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS 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 miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv892628	chr9:15420805-15528290	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv892629	chr9:15516375-15634326	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv968597	chr9:15522707-15527787	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15523000-15528200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:15524400-15525800	Enhancers	HUVEC	blood vessel
3	chr9:15525000-15525400	Enhancers	Brain Angular Gyrus	brain

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