Variant report

Variant	rs2287608
Chromosome Location	chr2:186679710-186679711
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:186669335..186673195-chr2:186676461..186681487,4	MCF-7	breast:
2	chr2:186677322..186681085-chr2:186681928..186686220,4	MCF-7	breast:

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1016410	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10173807	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];0.93[EUR][1000 genomes]
rs10192219	0.89[EUR][1000 genomes]
rs1116941	0.87[EUR][1000 genomes]
rs11893024	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes]
rs12464270	0.83[ASN][1000 genomes]
rs12464403	0.90[ASN][1000 genomes]
rs12464986	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12466093	0.83[ASN][1000 genomes]
rs12475622	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs12475752	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12478116	0.90[ASN][1000 genomes]
rs12615971	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12988839	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12988992	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12991700	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12994796	0.84[ASN][1000 genomes]
rs12998112	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12999848	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13002387	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13003744	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13004035	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs13015006	0.84[ASN][1000 genomes]
rs13027342	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13028347	0.85[EUR][1000 genomes]
rs1468956	0.87[EUR][1000 genomes]
rs1861896	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2216496	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs2255620	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2370475	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2370505	0.86[ASN][1000 genomes]
rs35986831	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs36011205	0.86[ASN][1000 genomes]
rs36026587	0.84[AFR][1000 genomes]
rs36035600	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs36114949	0.87[EUR][1000 genomes]
rs4263075	0.85[ASN][1000 genomes]
rs4343438	0.84[CEU][hapmap];0.97[GIH][hapmap]
rs4500902	0.92[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4561628	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4666691	0.89[ASN][1000 genomes]
rs4666692	0.86[ASN][1000 genomes]
rs4666697	0.85[CHD][hapmap];0.80[JPT][hapmap]
rs4667051	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4667052	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4667057	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4667064	0.84[ASN][1000 genomes]
rs4667065	0.84[ASN][1000 genomes]
rs4667066	0.84[ASN][1000 genomes]
rs58696152	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59190502	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs62199142	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62199145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62200894	0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs62200949	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6434137	0.86[EUR][1000 genomes]
rs6718246	0.84[EUR][1000 genomes]
rs67196811	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6725306	0.87[EUR][1000 genomes]
rs6733946	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6735082	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6745546	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs71407825	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7602728	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7605929	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs763330	0.88[EUR][1000 genomes]
rs984988	0.87[EUR][1000 genomes]
rs988937	0.88[EUR][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	nsv1007052	chr2:186441382-186864390	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv584019	chr2:186445393-186866874	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1009118	chr2:186450293-186864390	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1008230	chr2:186474069-186818718	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv536076	chr2:186474069-186818718	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv584021	chr2:186475590-186866841	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv875545	chr2:186566024-187280164	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv1796337	chr2:186618494-186704965	ZNF genes & repeats Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv1797599	chr2:186618494-186882821	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv817325	chr2:186625679-187200841	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv868949	chr2:186657142-187327560	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr2:186677000-186682800	Weak transcription	Left Ventricle	heart

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