Variant report

Variant	rs13409719
Chromosome Location	chr2:212814557-212814558
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10497954	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12613571	0.91[ASN][1000 genomes]
rs12617457	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs16847307	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16847322	1.00[ASN][1000 genomes]
rs16847346	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2102996	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs987321	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs987322	0.83[AMR][1000 genomes];1.00[ASN][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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv834525	chr2:212693190-212860356	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212806800-212816400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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

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