Variant report

Variant	rs9287229
Chromosome Location	chr1:239699124-239699125
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10495444	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12023096	0.86[EUR][1000 genomes]
rs1218661	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1218663	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1218664	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1218665	0.85[EUR][1000 genomes]
rs1218666	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1218667	0.87[EUR][1000 genomes]
rs1218668	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1218669	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1218670	0.88[EUR][1000 genomes]
rs1218672	0.87[EUR][1000 genomes]
rs1310402	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1625158	0.87[EUR][1000 genomes]
rs1628671	0.87[EUR][1000 genomes]
rs1782351	0.87[EUR][1000 genomes]
rs1782353	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1782354	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1782355	0.87[EUR][1000 genomes]
rs1782356	0.87[EUR][1000 genomes]
rs1782357	0.85[EUR][1000 genomes]
rs1796830	0.87[EUR][1000 genomes]
rs1796831	0.87[EUR][1000 genomes]
rs1796832	0.87[EUR][1000 genomes]
rs1796833	0.87[EUR][1000 genomes]
rs1796836	0.87[EUR][1000 genomes]
rs1796837	0.87[EUR][1000 genomes]
rs1899610	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1977746	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2248916	0.87[EUR][1000 genomes]
rs2248922	0.87[EUR][1000 genomes]
rs35366199	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4514231	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6676678	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72756737	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9428474	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9428475	0.88[EUR][1000 genomes]
rs9428476	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9428835	0.87[EUR][1000 genomes]
rs9428836	0.88[EUR][1000 genomes]
rs9428837	0.88[EUR][1000 genomes]
rs9428838	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002301	chr1:239182255-239774393	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv549435	chr1:239375010-239974006	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv833037	chr1:239522168-239699412	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3377526	chr1:239623743-240111639	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv873351	chr1:239636613-240324200	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 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	chr1:239680200-239700400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:239699000-239699200	Enhancers	Ovary	ovary
3	chr1:239699000-239699400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:239699000-239699400	Enhancers	Pancreas	Pancrea

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