Variant report

Variant	rs72862952
Chromosome Location	chr4:77270259-77270260
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs57389468	1.00[AMR][1000 genomes]
rs58041283	1.00[AMR][1000 genomes]
rs58343507	1.00[AMR][1000 genomes]
rs60983927	1.00[AMR][1000 genomes]
rs61494828	1.00[AMR][1000 genomes]
rs72858504	1.00[AMR][1000 genomes]
rs72858514	1.00[AMR][1000 genomes]
rs72858534	1.00[AMR][1000 genomes]
rs72858537	1.00[AMR][1000 genomes]
rs72858539	1.00[AMR][1000 genomes]
rs72858541	1.00[AMR][1000 genomes]
rs72858543	1.00[AMR][1000 genomes]
rs72858544	1.00[AMR][1000 genomes]
rs72858547	1.00[AMR][1000 genomes]
rs72858548	1.00[AMR][1000 genomes]
rs72858559	1.00[AMR][1000 genomes]
rs72858560	1.00[AMR][1000 genomes]
rs72858564	1.00[AMR][1000 genomes]
rs72858565	1.00[AMR][1000 genomes]
rs72858567	1.00[AMR][1000 genomes]
rs72858568	1.00[AMR][1000 genomes]
rs72858572	1.00[AMR][1000 genomes]
rs72858576	1.00[AMR][1000 genomes]
rs72858580	1.00[AMR][1000 genomes]
rs72858584	1.00[AMR][1000 genomes]
rs72858586	1.00[AMR][1000 genomes]
rs72858588	1.00[AMR][1000 genomes]
rs72858593	1.00[AMR][1000 genomes]
rs72858595	1.00[AMR][1000 genomes]
rs72862912	1.00[AFR][1000 genomes]
rs72862990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72864608	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72864636	1.00[AMR][1000 genomes]
rs72864651	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72866508	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	esv2757941	chr4:77264596-77417457	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2759262	chr4:77264596-77455405	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr4:77270000-77270400	Strong transcription	Liver	Liver
2	chr4:77270200-77272800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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Input of quick search could be:

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

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