Variant report

Variant	rs1933582
Chromosome Location	chr9:84967534-84967535
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10867835	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10867836	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10867837	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10867839	0.87[JPT][hapmap]
rs10867840	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10867844	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11139554	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1888327	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1933580	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1933583	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2774634	0.99[ASN][1000 genomes]
rs2774635	0.94[ASN][1000 genomes]
rs2788109	0.94[ASN][1000 genomes]
rs2788110	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2788112	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2788113	0.83[AMR][1000 genomes]
rs35064221	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4276765	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4338186	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4563967	0.91[JPT][hapmap]
rs4877229	1.00[CEU][hapmap];0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4877231	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6559659	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7020546	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7021352	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7047870	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7848263	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7848823	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7849168	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9410578	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893507	chr9:84799537-85097651	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893508	chr9:84954592-85080395	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv893509	chr9:84954592-85097651	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893510	chr9:84954592-85117420	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:84964200-84968000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:84967400-84970000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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