Variant report

Variant	rs2037834
Chromosome Location	chr11:23955572-23955573
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10500971	0.93[EUR][1000 genomes]
rs10734347	0.92[ASN][1000 genomes]
rs10742018	0.92[ASN][1000 genomes]
rs10742019	0.86[ASN][1000 genomes]
rs10742020	0.92[ASN][1000 genomes]
rs10742021	0.92[ASN][1000 genomes]
rs10767145	0.92[ASN][1000 genomes]
rs10834241	0.81[ASN][1000 genomes]
rs10834242	0.93[ASN][1000 genomes]
rs10834247	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10834248	0.90[ASN][1000 genomes]
rs11027639	0.93[EUR][1000 genomes]
rs11823765	0.95[EUR][1000 genomes]
rs11825108	0.95[EUR][1000 genomes]
rs11825842	0.91[EUR][1000 genomes]
rs11825890	0.93[EUR][1000 genomes]
rs11825892	0.93[EUR][1000 genomes]
rs11827016	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11827659	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11828069	0.95[EUR][1000 genomes]
rs16911969	0.93[EUR][1000 genomes]
rs16911972	0.93[EUR][1000 genomes]
rs1879230	0.88[ASN][1000 genomes]
rs1915068	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1915069	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2176788	0.93[EUR][1000 genomes]
rs2403865	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4244510	0.92[ASN][1000 genomes]
rs4244511	0.90[ASN][1000 genomes]
rs4506647	0.95[EUR][1000 genomes]
rs4923145	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55988898	0.93[EUR][1000 genomes]
rs6483998	0.94[ASN][1000 genomes]
rs6483999	0.92[ASN][1000 genomes]
rs6484003	0.93[EUR][1000 genomes]
rs7104264	0.95[EUR][1000 genomes]
rs7104524	0.95[EUR][1000 genomes]
rs7105348	0.92[ASN][1000 genomes]
rs7106159	0.93[EUR][1000 genomes]
rs7112747	0.95[EUR][1000 genomes]
rs7129003	0.82[ASN][1000 genomes]
rs7130113	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7930923	0.95[EUR][1000 genomes]
rs7932515	0.81[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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23954800-23955600	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr11:23955000-23955600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:23955000-23955600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:23955400-23955800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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