Variant report

Variant	rs73137211
Chromosome Location	chr7:78413357-78413358
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10953687	1.00[ASN][1000 genomes]
rs12113058	1.00[ASN][1000 genomes]
rs12534800	1.00[ASN][1000 genomes]
rs12536030	1.00[ASN][1000 genomes]
rs12536979	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28650857	0.83[ASN][1000 genomes]
rs66495951	0.83[ASN][1000 genomes]
rs73135526	1.00[ASN][1000 genomes]
rs73135549	1.00[ASN][1000 genomes]
rs73135595	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73135599	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73137205	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73137209	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73365873	1.00[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	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv949647	chr7:78406281-78495913	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78412600-78413400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr7:78412800-78413800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:78412800-78414000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:78413000-78413400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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

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