Variant report

Variant	rs73278270
Chromosome Location	chr12:42388610-42388611
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1683193	0.85[AMR][1000 genomes]
rs56669009	0.85[AMR][1000 genomes]
rs56856898	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56945323	0.85[AMR][1000 genomes]
rs57582332	0.85[AMR][1000 genomes]
rs58108857	1.00[AMR][1000 genomes]
rs58417163	0.85[AMR][1000 genomes]
rs59451068	0.85[AMR][1000 genomes]
rs59477321	1.00[AMR][1000 genomes]
rs60327465	0.85[AMR][1000 genomes]
rs60655395	0.85[AMR][1000 genomes]
rs712113	0.85[AMR][1000 genomes]
rs712117	0.85[AMR][1000 genomes]
rs7132315	0.85[AMR][1000 genomes]
rs7133783	0.85[AMR][1000 genomes]
rs7298660	0.85[AMR][1000 genomes]
rs73278268	0.85[AMR][1000 genomes]
rs73278272	0.85[AMR][1000 genomes]
rs73278295	0.85[AMR][1000 genomes]
rs73278297	0.85[AMR][1000 genomes]
rs73278298	0.85[AMR][1000 genomes]
rs73278299	0.85[AMR][1000 genomes]
rs73280016	0.85[AMR][1000 genomes]
rs73280025	0.85[AMR][1000 genomes]
rs73280038	1.00[AMR][1000 genomes]
rs73280040	0.85[AMR][1000 genomes]
rs73280047	0.85[AMR][1000 genomes]
rs73280057	1.00[AMR][1000 genomes]
rs73280063	0.85[AMR][1000 genomes]
rs73280071	0.85[AMR][1000 genomes]
rs73280079	0.85[AMR][1000 genomes]
rs73280085	0.85[AMR][1000 genomes]
rs73280087	0.85[AMR][1000 genomes]
rs73280101	0.85[AMR][1000 genomes]
rs73281848	0.85[AMR][1000 genomes]
rs7954844	0.85[AMR][1000 genomes]
rs7960285	0.85[AMR][1000 genomes]
rs850828	0.85[AMR][1000 genomes]
rs864291	0.85[AMR][1000 genomes]
rs864298	0.85[AMR][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	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv832387	chr12:42345541-42465505	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr12:42387600-42390400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:42388600-42389800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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