Variant report

Variant	rs72916833
Chromosome Location	chr3:47577277-47577278
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:6)

rs_ID	r²[population]
rs17079693	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6807733	0.87[AFR][1000 genomes]
rs6810322	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs72916824	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs72916838	0.86[AFR][1000 genomes]
rs73834334	0.87[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	nsv876756	chr3:47002931-47586514	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	esv33034	chr3:47565429-47578605	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47576800-47579800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr3:47577000-47578200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:47577000-47583000	Weak transcription	K562	blood

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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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