Variant report

Variant	rs10834243
Chromosome Location	chr11:23961256-23961257
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10734347	0.90[EUR][1000 genomes]
rs10742018	0.93[EUR][1000 genomes]
rs10742019	0.93[EUR][1000 genomes]
rs10742020	0.94[EUR][1000 genomes]
rs10742021	0.94[EUR][1000 genomes]
rs10767145	0.89[EUR][1000 genomes]
rs10834242	0.83[EUR][1000 genomes]
rs10834247	0.94[EUR][1000 genomes]
rs10834248	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1879230	0.94[EUR][1000 genomes]
rs1915053	0.89[EUR][1000 genomes]
rs2955452	0.89[EUR][1000 genomes]
rs35758121	0.90[ASN][1000 genomes]
rs4244510	0.94[EUR][1000 genomes]
rs4244511	0.90[EUR][1000 genomes]
rs4291675	0.91[ASN][1000 genomes]
rs4540837	0.86[ASN][1000 genomes]
rs56962830	0.81[EUR][1000 genomes]
rs61392438	0.86[ASN][1000 genomes]
rs6483998	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6483999	0.93[EUR][1000 genomes]
rs7105348	0.93[EUR][1000 genomes]
rs7938829	0.87[EUR][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	nsv897062	chr11:23687928-24031627	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916840	chr11:23710275-24064119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:23956400-23963800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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