Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:15368518..15371257-chr11:15372733..15374518,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10766234	0.85[ASN][1000 genomes]
rs10766235	0.85[ASN][1000 genomes]
rs10766240	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11023529	0.85[ASN][1000 genomes]
rs11023533	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11023539	0.92[AFR][1000 genomes]
rs12794836	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4356209	0.83[AFR][1000 genomes]
rs4381353	0.83[AFR][1000 genomes]
rs4548599	0.85[ASN][1000 genomes]
rs4622244	0.87[ASN][1000 genomes]
rs4756805	0.85[ASN][1000 genomes]
rs4757307	1.00[ASN][1000 genomes]
rs55735037	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61878035	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6486240	0.90[AFR][1000 genomes]
rs7105245	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7111340	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7125905	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7479972	0.81[AFR][1000 genomes]
rs7927667	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830370	chr11:15142247-15444094	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv832072	chr11:15226843-15392190	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1044103	chr11:15345545-15390081	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3387855	chr11:15371576-15376774	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3384007	chr11:15371976-15375674	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15364600-15386000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

Quick Search: