Variant report

Variant	rs35735503
Chromosome Location	chr2:172493244-172493245
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	chr2:172487381..172489786-chr2:172492244..172493876,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10185715	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10432421	0.84[EUR][1000 genomes]
rs10432422	0.83[EUR][1000 genomes]
rs10432469	0.80[EUR][1000 genomes]
rs10432470	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10432471	0.82[ASN][1000 genomes]
rs10432472	0.84[EUR][1000 genomes]
rs10432473	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11674857	0.89[EUR][1000 genomes]
rs11680728	0.89[ASN][1000 genomes]
rs11693157	0.90[ASN][1000 genomes]
rs12618717	0.90[ASN][1000 genomes]
rs12622021	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12991896	0.90[ASN][1000 genomes]
rs12997634	0.90[ASN][1000 genomes]
rs13002792	0.81[ASN][1000 genomes]
rs13016328	0.90[ASN][1000 genomes]
rs13025856	0.90[ASN][1000 genomes]
rs1399960	0.91[ASN][1000 genomes]
rs1533417	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1543128	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1554157	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1554158	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1606926	0.81[ASN][1000 genomes]
rs1969271	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2037158	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2037159	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2037160	0.81[ASN][1000 genomes]
rs2037161	0.82[ASN][1000 genomes]
rs2037163	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2102739	0.81[ASN][1000 genomes]
rs2102740	0.90[ASN][1000 genomes]
rs2138350	0.91[ASN][1000 genomes]
rs2176150	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2356796	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2356797	0.83[ASN][1000 genomes]
rs2884028	0.81[ASN][1000 genomes]
rs28893802	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34054455	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34919335	0.85[ASN][1000 genomes]
rs4264541	0.89[EUR][1000 genomes]
rs4265979	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4265980	0.88[ASN][1000 genomes]
rs4668395	0.84[EUR][1000 genomes]
rs4668396	0.90[ASN][1000 genomes]
rs4668397	0.83[EUR][1000 genomes]
rs57130402	0.85[ASN][1000 genomes]
rs59567105	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6433301	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6433302	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6433305	0.90[ASN][1000 genomes]
rs6704691	0.82[ASN][1000 genomes]
rs6718546	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6723896	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6725338	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6743208	0.90[ASN][1000 genomes]
rs6747069	0.90[ASN][1000 genomes]
rs6754595	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7562302	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7571192	0.82[EUR][1000 genomes]
rs7575168	0.81[ASN][1000 genomes]
rs7592639	0.90[ASN][1000 genomes]
rs7606149	0.92[ASN][1000 genomes]
rs7606189	0.90[ASN][1000 genomes]
rs7606481	0.90[ASN][1000 genomes]
rs908371	0.90[ASN][1000 genomes]
rs9287946	0.89[EUR][1000 genomes]
rs9678221	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs997635	0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997638	chr2:172442205-172560406	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 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	chr2:172493200-172499400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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