Variant report

Variant	rs11038436
Chromosome Location	chr11:45411272-45411273
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	chr11:45402149..45405049-chr11:45410823..45413385,2	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10501315	0.83[AMR][1000 genomes]
rs11038423	0.85[AMR][1000 genomes]
rs11038424	0.85[AMR][1000 genomes]
rs11038426	0.85[AMR][1000 genomes]
rs11038427	0.85[AMR][1000 genomes]
rs11038429	0.85[AMR][1000 genomes]
rs11038430	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11038431	0.85[AMR][1000 genomes]
rs11038432	0.85[AMR][1000 genomes]
rs11038433	0.92[AMR][1000 genomes]
rs11038434	1.00[AMR][1000 genomes]
rs11038435	1.00[AMR][1000 genomes]
rs11038437	1.00[AMR][1000 genomes]
rs11038442	1.00[AMR][1000 genomes]
rs11038443	1.00[AMR][1000 genomes]
rs11038444	1.00[AMR][1000 genomes]
rs11038450	1.00[AMR][1000 genomes]
rs11038451	1.00[AMR][1000 genomes]
rs11038455	0.83[AMR][1000 genomes]
rs11038456	0.83[AMR][1000 genomes]
rs11038457	0.83[AMR][1000 genomes]
rs11038458	0.83[AMR][1000 genomes]
rs11038459	0.83[AMR][1000 genomes]
rs11038461	0.83[AMR][1000 genomes]
rs11038462	0.83[AMR][1000 genomes]
rs11038465	0.83[AMR][1000 genomes]
rs11038466	0.83[AMR][1000 genomes]
rs11038467	0.83[AMR][1000 genomes]
rs11038469	0.83[AMR][1000 genomes]
rs11038471	0.83[AMR][1000 genomes]
rs11038473	0.83[AMR][1000 genomes]
rs11038474	0.83[AMR][1000 genomes]
rs11038475	0.83[AMR][1000 genomes]
rs11038477	0.83[AMR][1000 genomes]
rs11038479	0.83[AMR][1000 genomes]
rs11038481	0.83[AMR][1000 genomes]
rs11038482	0.83[AMR][1000 genomes]
rs11038483	0.83[AMR][1000 genomes]
rs11038485	0.83[AMR][1000 genomes]
rs11038486	0.83[AMR][1000 genomes]
rs11038487	0.83[AMR][1000 genomes]
rs11038491	0.83[AMR][1000 genomes]
rs11038492	0.83[AMR][1000 genomes]
rs11038493	0.83[AMR][1000 genomes]
rs11038494	0.83[AMR][1000 genomes]
rs11038495	0.83[AMR][1000 genomes]
rs11038497	0.83[AMR][1000 genomes]
rs11038498	0.83[AMR][1000 genomes]
rs1107209	0.83[AMR][1000 genomes]
rs11601006	0.85[AMR][1000 genomes]
rs11820242	0.89[ASN][1000 genomes]
rs11829008	0.86[ASN][1000 genomes]
rs12361372	0.83[AMR][1000 genomes]
rs12365430	0.83[AMR][1000 genomes]
rs1488668	0.83[AMR][1000 genomes]
rs1488670	0.83[AMR][1000 genomes]
rs17723819	0.83[AMR][1000 genomes]
rs17724032	0.83[AMR][1000 genomes]
rs17785901	0.83[AMR][1000 genomes]
rs2044877	0.85[AMR][1000 genomes]
rs5015616	0.89[ASN][1000 genomes]
rs72897475	1.00[AMR][1000 genomes]
rs72899480	1.00[AMR][1000 genomes]
rs72899488	1.00[AMR][1000 genomes]
rs72901403	0.83[AMR][1000 genomes]
rs72901422	0.83[AMR][1000 genomes]
rs72901426	0.83[AMR][1000 genomes]
rs72901447	0.83[AMR][1000 genomes]
rs72901450	0.83[AMR][1000 genomes]
rs72901459	0.83[AMR][1000 genomes]
rs72901500	0.83[AMR][1000 genomes]
rs72903035	0.83[AMR][1000 genomes]
rs72903086	0.83[AMR][1000 genomes]
rs72903094	0.83[AMR][1000 genomes]
rs72905021	0.83[AMR][1000 genomes]
rs72905025	0.83[AMR][1000 genomes]
rs72905093	0.83[AMR][1000 genomes]
rs72906922	0.83[AMR][1000 genomes]
rs72906947	0.83[AMR][1000 genomes]
rs73456039	0.81[ASN][1000 genomes]
rs971897	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv467869	chr11:45389225-45415035	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv554185	chr11:45389225-45415035	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45405400-45434800	Weak transcription	Right Atrium	heart
2	chr11:45407000-45421000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:45407600-45414000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:45409200-45412200	Enhancers	Fetal Brain Female	brain
5	chr11:45409400-45413000	Enhancers	Brain Germinal Matrix	brain
6	chr11:45409800-45413800	Enhancers	Ovary	ovary
7	chr11:45410600-45412000	Bivalent Enhancer	HepG2	liver
8	chr11:45410800-45412000	Weak transcription	Fetal Brain Male	brain
9	chr11:45411000-45412600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:45411200-45417000	Enhancers	Liver	Liver

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