Variant report

Variant	rs72988173
Chromosome Location	chr2:141627655-141627656
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs57626670	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6713857	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6750037	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6755167	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72988157	0.87[AFR][1000 genomes]
rs72988163	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72988176	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72988202	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72990112	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72990118	0.80[AFR][1000 genomes];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	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1003008	chr2:141518795-141763505	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:141626400-141630800	Enhancers	Liver	Liver
2	chr2:141627400-141628000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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