Variant report

Variant	rs2860735
Chromosome Location	chr2:76537978-76537979
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	chr2:76536543..76538658-chr2:76539286..76540999,2	MCF-7	breast:

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10084237	0.96[EUR][1000 genomes]
rs10169075	0.96[EUR][1000 genomes]
rs10170747	0.91[EUR][1000 genomes]
rs11126521	0.91[EUR][1000 genomes]
rs11673996	0.96[EUR][1000 genomes]
rs11896158	1.00[EUR][1000 genomes]
rs12328296	1.00[EUR][1000 genomes]
rs12476472	0.96[EUR][1000 genomes]
rs12477363	0.91[EUR][1000 genomes]
rs12987628	0.96[EUR][1000 genomes]
rs12989829	0.84[EUR][1000 genomes]
rs13005979	1.00[EUR][1000 genomes]
rs13014046	0.91[EUR][1000 genomes]
rs1358177	1.00[EUR][1000 genomes]
rs1358178	1.00[EUR][1000 genomes]
rs1358180	1.00[EUR][1000 genomes]
rs1358181	1.00[EUR][1000 genomes]
rs1401837	0.96[EUR][1000 genomes]
rs1401843	1.00[EUR][1000 genomes]
rs1401844	1.00[EUR][1000 genomes]
rs1405339	0.96[EUR][1000 genomes]
rs1405340	0.96[EUR][1000 genomes]
rs1405341	0.96[EUR][1000 genomes]
rs1405345	1.00[EUR][1000 genomes]
rs1519897	1.00[EUR][1000 genomes]
rs1526613	1.00[EUR][1000 genomes]
rs1526622	0.96[EUR][1000 genomes]
rs1526625	0.96[EUR][1000 genomes]
rs1526626	0.96[EUR][1000 genomes]
rs1526628	0.96[EUR][1000 genomes]
rs1526640	1.00[EUR][1000 genomes]
rs1526642	0.91[EUR][1000 genomes]
rs1526646	0.91[EUR][1000 genomes]
rs1526648	0.91[EUR][1000 genomes]
rs1526650	0.91[EUR][1000 genomes]
rs1526651	0.91[EUR][1000 genomes]
rs1526652	0.91[EUR][1000 genomes]
rs1526653	0.91[EUR][1000 genomes]
rs1609009	0.96[EUR][1000 genomes]
rs1852364	1.00[EUR][1000 genomes]
rs1880282	0.91[EUR][1000 genomes]
rs1880283	0.91[EUR][1000 genomes]
rs1880284	0.91[EUR][1000 genomes]
rs1949923	0.96[EUR][1000 genomes]
rs1980323	0.91[EUR][1000 genomes]
rs2049550	1.00[EUR][1000 genomes]
rs2090688	0.96[EUR][1000 genomes]
rs2139466	1.00[EUR][1000 genomes]
rs2139468	0.96[EUR][1000 genomes]
rs2139469	1.00[EUR][1000 genomes]
rs2860734	0.96[EUR][1000 genomes]
rs2860736	1.00[EUR][1000 genomes]
rs2860741	1.00[EUR][1000 genomes]
rs2860742	0.91[EUR][1000 genomes]
rs3961977	1.00[EUR][1000 genomes]
rs3980323	0.82[EUR][1000 genomes]
rs4241268	0.82[EUR][1000 genomes]
rs4444560	0.96[EUR][1000 genomes]
rs4852401	1.00[EUR][1000 genomes]
rs4852404	0.91[EUR][1000 genomes]
rs4853208	0.96[EUR][1000 genomes]
rs4853224	1.00[EUR][1000 genomes]
rs4853225	1.00[EUR][1000 genomes]
rs4853235	0.88[EUR][1000 genomes]
rs4853236	0.96[EUR][1000 genomes]
rs4853237	1.00[EUR][1000 genomes]
rs4853239	1.00[EUR][1000 genomes]
rs4853240	1.00[EUR][1000 genomes]
rs6547060	0.96[EUR][1000 genomes]
rs6547062	1.00[EUR][1000 genomes]
rs6547063	1.00[EUR][1000 genomes]
rs6547074	0.91[EUR][1000 genomes]
rs6547076	0.91[EUR][1000 genomes]
rs6547077	0.91[EUR][1000 genomes]
rs6547081	1.00[EUR][1000 genomes]
rs6714618	1.00[EUR][1000 genomes]
rs6718886	1.00[EUR][1000 genomes]
rs6725074	1.00[EUR][1000 genomes]
rs6731474	1.00[EUR][1000 genomes]
rs6738864	0.91[EUR][1000 genomes]
rs6742237	0.91[EUR][1000 genomes]
rs6743857	0.96[EUR][1000 genomes]
rs6747521	1.00[EUR][1000 genomes]
rs6758608	0.96[EUR][1000 genomes]
rs7424136	1.00[EUR][1000 genomes]
rs7566339	1.00[EUR][1000 genomes]
rs7566454	1.00[EUR][1000 genomes]
rs7587657	1.00[EUR][1000 genomes]
rs7601253	1.00[EUR][1000 genomes]
rs7602197	1.00[EUR][1000 genomes]
rs908960	1.00[EUR][1000 genomes]
rs964439	1.00[EUR][1000 genomes]
rs964440	1.00[EUR][1000 genomes]
rs964441	1.00[EUR][1000 genomes]
rs964443	1.00[EUR][1000 genomes]
rs975901	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006097	chr2:76524248-76675427	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv519947	chr2:76537604-76588942	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76537000-76542400	Enhancers	Hela-S3	cervix
2	chr2:76537800-76538200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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