Variant report

Variant	rs1418765
Chromosome Location	chr1:58615545-58615546
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10493244	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11799299	0.91[EUR][1000 genomes]
rs11799320	0.91[EUR][1000 genomes]
rs11801568	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11802821	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11809707	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12025945	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12034198	0.99[ASN][1000 genomes]
rs12040062	0.94[ASN][1000 genomes]
rs12048970	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12565486	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12565597	0.97[ASN][1000 genomes]
rs13374932	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1416341	1.00[ASN][1000 genomes]
rs1416343	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1416344	0.82[EUR][1000 genomes]
rs17116988	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17117013	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17117039	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17117108	0.88[EUR][1000 genomes]
rs17117128	0.82[EUR][1000 genomes]
rs1832488	0.88[EUR][1000 genomes]
rs1832489	0.90[EUR][1000 genomes]
rs1992481	0.91[EUR][1000 genomes]
rs2406591	0.98[ASN][1000 genomes]
rs35995264	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3850534	0.94[ASN][1000 genomes]
rs3850535	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3850536	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4406656	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59675977	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs59994009	0.90[EUR][1000 genomes]
rs60060991	0.90[EUR][1000 genomes]
rs60112110	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6667829	0.99[ASN][1000 genomes]
rs6701275	0.99[ASN][1000 genomes]
rs74074110	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74074991	0.92[EUR][1000 genomes]
rs74074993	0.91[EUR][1000 genomes]
rs74075932	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74075933	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74075935	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74075938	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74076072	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74076075	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74076076	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs74076078	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7551611	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1008968	chr1:58582159-58982440	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv534974	chr1:58582159-58982440	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	esv994666	chr1:58612446-58615559	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58613600-58616200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:58615000-58616000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:58615000-58616000	Enhancers	Liver	Liver

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