Variant report

Variant	rs10941665
Chromosome Location	chr5:44398696-44398697
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10041294	0.96[EUR][1000 genomes]
rs10052488	0.98[EUR][1000 genomes]
rs10055789	0.99[EUR][1000 genomes]
rs10055953	0.99[EUR][1000 genomes]
rs10077856	0.99[EUR][1000 genomes]
rs10462073	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10472394	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10473354	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11948749	0.96[EUR][1000 genomes]
rs12054807	0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13357659	0.96[EUR][1000 genomes]
rs1384451	0.98[EUR][1000 genomes]
rs1482667	0.99[EUR][1000 genomes]
rs1482668	0.99[EUR][1000 genomes]
rs1482685	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1531804	0.98[EUR][1000 genomes]
rs2200123	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2330551	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2330553	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2330554	0.99[EUR][1000 genomes]
rs2877162	0.99[EUR][1000 genomes]
rs2877163	0.99[EUR][1000 genomes]
rs4146354	0.99[EUR][1000 genomes]
rs4242112	0.99[EUR][1000 genomes]
rs4314404	0.97[EUR][1000 genomes]
rs4866897	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6874246	0.99[EUR][1000 genomes]
rs6893275	0.99[EUR][1000 genomes]
rs7356597	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs922852	0.99[EUR][1000 genomes]
rs9292906	0.99[EUR][1000 genomes]
rs973843	0.99[EUR][1000 genomes]
rs973844	0.95[EUR][1000 genomes]
rs987852	0.99[EUR][1000 genomes]
rs9885121	0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830277	chr5:44383402-44566881	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:44395200-44447400	Weak transcription	Fetal Lung	lung
2	chr5:44395600-44403000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:44396600-44403000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:44397200-44399400	Weak transcription	Pancreas	Pancrea
5	chr5:44398600-44399000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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