Variant report

Variant	rs11120531
Chromosome Location	chr1:215417312-215417313
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	chr1:215361168..215363733-chr1:215415498..215417578,2	MCF-7	breast:
2	chr1:215409558..215413015-chr1:215413539..215417993,3	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10494997	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10779654	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10779655	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10864162	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10864163	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10864164	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11120522	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11120528	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120540	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11811604	0.91[EUR][1000 genomes]
rs12026152	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12080135	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12131712	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12142076	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12567503	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1339399	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1339400	0.82[ASN][1000 genomes]
rs1361342	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1416651	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1416656	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2202679	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4113098	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4281301	0.94[EUR][1000 genomes]
rs4360503	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4539107	0.89[EUR][1000 genomes]
rs4633261	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4655280	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6664253	0.82[EUR][1000 genomes]
rs6671986	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6674923	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72737267	0.82[ASN][1000 genomes]
rs7512197	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7516344	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7547867	0.90[EUR][1000 genomes];0.85[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	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
2	nsv873170	chr1:215367248-215440975	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215413400-215420200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:215415600-215418400	Enhancers	Fetal Stomach	stomach
3	chr1:215416800-215417400	Enhancers	Osteobl	bone

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