Variant report

Variant	rs2541015
Chromosome Location	chr2:67748604-67748605
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67746421..67749968-chr2:68288445..68290410,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197223	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10207998	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1023691	1.00[ASN][1000 genomes]
rs1023693	1.00[ASN][1000 genomes]
rs11126134	1.00[ASN][1000 genomes]
rs11126138	1.00[ASN][1000 genomes]
rs11900280	1.00[ASN][1000 genomes]
rs12998432	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12998660	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13016594	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13022809	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1430789	1.00[ASN][1000 genomes]
rs1430790	1.00[ASN][1000 genomes]
rs1430791	1.00[ASN][1000 genomes]
rs1430792	1.00[ASN][1000 genomes]
rs1521050	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1521052	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1568469	0.91[EUR][1000 genomes]
rs17033691	1.00[ASN][1000 genomes]
rs2541028	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2541030	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2541031	0.91[EUR][1000 genomes]
rs2541034	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683676	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683682	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683683	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2861640	1.00[ASN][1000 genomes]
rs2861644	1.00[ASN][1000 genomes]
rs2861645	1.00[ASN][1000 genomes]
rs2861648	1.00[ASN][1000 genomes]
rs2861681	1.00[ASN][1000 genomes]
rs2861686	1.00[ASN][1000 genomes]
rs2861687	1.00[ASN][1000 genomes]
rs2861689	1.00[ASN][1000 genomes]
rs2861698	1.00[ASN][1000 genomes]
rs2861700	1.00[ASN][1000 genomes]
rs2861701	1.00[ASN][1000 genomes]
rs2861703	1.00[ASN][1000 genomes]
rs2902007	1.00[ASN][1000 genomes]
rs2902008	1.00[ASN][1000 genomes]
rs2902023	1.00[ASN][1000 genomes]
rs2902025	1.00[ASN][1000 genomes]
rs35250398	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4260227	1.00[ASN][1000 genomes]
rs4362541	1.00[ASN][1000 genomes]
rs4381768	1.00[ASN][1000 genomes]
rs4533457	1.00[ASN][1000 genomes]
rs4671806	1.00[ASN][1000 genomes]
rs4671811	1.00[ASN][1000 genomes]
rs4671812	1.00[ASN][1000 genomes]
rs4671813	1.00[ASN][1000 genomes]
rs4671817	1.00[ASN][1000 genomes]
rs6546317	1.00[ASN][1000 genomes]
rs6546318	1.00[ASN][1000 genomes]
rs6546320	1.00[ASN][1000 genomes]
rs6546322	1.00[ASN][1000 genomes]
rs6717863	1.00[ASN][1000 genomes]
rs6724133	1.00[ASN][1000 genomes]
rs6730286	1.00[ASN][1000 genomes]
rs6746394	1.00[ASN][1000 genomes]
rs6752799	1.00[ASN][1000 genomes]
rs7425711	1.00[ASN][1000 genomes]
rs7569813	1.00[ASN][1000 genomes]
rs7595894	1.00[ASN][1000 genomes]
rs7598280	1.00[ASN][1000 genomes]
rs9309402	1.00[ASN][1000 genomes]
rs980227	1.00[ASN][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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	esv3335541	chr2:67577544-67773907	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67745000-67749800	Weak transcription	Fetal Kidney	kidney
2	chr2:67745200-67749000	Weak transcription	Fetal Stomach	stomach
3	chr2:67745200-67750200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:67745400-67749600	Weak transcription	Fetal Lung	lung

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