Variant report

Variant	rs73465381
Chromosome Location	chr9:73741824-73741825
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs57535377	1.00[AMR][1000 genomes]
rs57728903	1.00[AMR][1000 genomes]
rs60573626	1.00[AMR][1000 genomes]
rs61198146	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61687197	0.82[AFR][1000 genomes]
rs73467727	1.00[AMR][1000 genomes]
rs73467749	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035505	chr9:73709852-73934353	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73737000-73742600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:73738800-73743800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:73739000-73745800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:73740200-73742400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:73740400-73758400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:73741800-73742400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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