Variant report

Variant	rs17604588
Chromosome Location	chr2:31649666-31649667
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	chr2:31647816..31650394-chr2:31651121..31653448,2	K562	blood:
2	chr2:31648749..31651187-chr2:31653757..31655577,2	MCF-7	breast:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1033688	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1033689	0.93[ASN][1000 genomes]
rs1033690	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11124260	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11124261	0.92[ASN][1000 genomes]
rs11526116	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11526117	0.90[ASN][1000 genomes]
rs11674100	0.96[ASN][1000 genomes]
rs11679875	0.89[ASN][1000 genomes]
rs12467131	0.83[ASN][1000 genomes]
rs12468955	0.93[ASN][1000 genomes]
rs12469125	0.93[ASN][1000 genomes]
rs12473298	0.92[ASN][1000 genomes]
rs12479415	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17545406	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17545483	0.94[ASN][1000 genomes]
rs17604831	0.93[ASN][1000 genomes]
rs1884723	0.92[ASN][1000 genomes]
rs1978638	0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1978639	0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs206806	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs206811	0.81[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs206816	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2163058	0.97[ASN][1000 genomes]
rs2365772	0.94[ASN][1000 genomes]
rs2365778	0.84[ASN][1000 genomes]
rs28810790	0.81[EUR][1000 genomes]
rs28815209	0.93[ASN][1000 genomes]
rs28879135	0.93[ASN][1000 genomes]
rs34096339	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4622775	0.91[ASN][1000 genomes]
rs4952215	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4952236	0.97[ASN][1000 genomes]
rs4952251	0.90[ASN][1000 genomes]
rs4952263	0.89[ASN][1000 genomes]
rs55933129	0.94[ASN][1000 genomes]
rs56247470	0.92[ASN][1000 genomes]
rs56271553	0.84[ASN][1000 genomes]
rs58071748	0.98[ASN][1000 genomes]
rs58364223	0.84[ASN][1000 genomes]
rs58967340	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59770035	0.93[ASN][1000 genomes]
rs59964343	0.98[ASN][1000 genomes]
rs60441502	0.90[ASN][1000 genomes]
rs60989770	0.93[ASN][1000 genomes]
rs61316601	0.86[ASN][1000 genomes]
rs61706447	0.96[ASN][1000 genomes]
rs62141223	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66492775	0.98[ASN][1000 genomes]
rs67603251	0.92[ASN][1000 genomes]
rs67830899	0.97[ASN][1000 genomes]
rs72790682	0.96[ASN][1000 genomes]
rs72794621	0.86[ASN][1000 genomes]
rs7575607	0.94[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7585845	0.93[ASN][1000 genomes]
rs7595578	0.98[ASN][1000 genomes]
rs7602067	0.91[ASN][1000 genomes]
rs766273	0.93[ASN][1000 genomes]
rs9636426	0.88[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	nsv949028	chr2:31502801-31665108	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv532648	chr2:31591498-32312698	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv456030	chr2:31598823-31820256	Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv456041	chr2:31598823-31820256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv581269	chr2:31598823-31820256	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv998853	chr2:31601455-31858961	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1005565	chr2:31603134-31868877	Genic enhancers Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1007179	chr2:31616112-31835410	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1005032	chr2:31616112-31867450	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1013891	chr2:31629179-31854283	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv535612	chr2:31629179-31854283	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31644200-31650600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:31644800-31650600	Weak transcription	Placenta	Placenta
3	chr2:31645000-31651000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:31648600-31654200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr2:31649200-31649800	Enhancers	HMEC	breast
6	chr2:31649400-31649800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:31649400-31650000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:31649600-31649800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:31649600-31652200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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