Variant report

Variant	rs72923913
Chromosome Location	chr3:88668584-88668585
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs72921987	0.80[AFR][1000 genomes]
rs72921996	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923928	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923953	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7638547	1.00[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	nsv916330	chr3:88083580-88884125	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1014703	chr3:88623532-88733631	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88666000-88669000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:88667800-88675400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:88668000-88669800	Weak transcription	Brain Germinal Matrix	brain
4	chr3:88668400-88668600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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

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