Variant report

Variant	rs73647949
Chromosome Location	chr9:73744401-73744402
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56962891	1.00[AMR][1000 genomes]
rs7018775	1.00[AMR][1000 genomes]
rs73647184	1.00[AMR][1000 genomes]
rs73647933	1.00[AMR][1000 genomes]
rs73647934	1.00[AMR][1000 genomes]
rs73647939	1.00[AMR][1000 genomes]
rs73647940	1.00[AMR][1000 genomes]
rs73647943	1.00[AMR][1000 genomes]
rs73647962	0.83[AFR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73739000-73745800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:73740400-73758400	Weak transcription	H1 Derived Neuronal Progenitor 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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