Variant report

Variant	rs9407660
Chromosome Location	chr9:15839292-15839293
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1009468	0.90[ASN][1000 genomes]
rs10738415	0.88[ASN][1000 genomes]
rs10756709	0.80[EUR][1000 genomes]
rs10756710	0.81[EUR][1000 genomes]
rs1081245	0.90[ASN][1000 genomes]
rs10962170	0.81[ASN][1000 genomes]
rs10962171	0.81[ASN][1000 genomes]
rs12377532	0.88[ASN][1000 genomes]
rs1572978	0.82[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2066292	0.95[ASN][1000 genomes]
rs2153725	0.91[ASN][1000 genomes]
rs2153726	0.94[ASN][1000 genomes]
rs2153727	0.91[ASN][1000 genomes]
rs2185665	0.91[ASN][1000 genomes]
rs2382553	0.82[ASN][1000 genomes]
rs2891007	0.89[ASN][1000 genomes]
rs7019205	0.90[ASN][1000 genomes]
rs7024440	0.90[ASN][1000 genomes]
rs7032457	0.91[ASN][1000 genomes]
rs7032634	0.91[ASN][1000 genomes]
rs7047045	0.91[ASN][1000 genomes]
rs7470881	0.82[ASN][1000 genomes]
rs770191	0.81[ASN][1000 genomes]
rs7853744	0.91[ASN][1000 genomes]
rs7857126	0.91[ASN][1000 genomes]
rs7857495	0.82[ASN][1000 genomes]
rs7866641	0.81[ASN][1000 genomes]
rs7871232	0.82[ASN][1000 genomes]
rs9298738	0.95[ASN][1000 genomes]
rs9298739	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9298740	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9298741	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9406536	0.82[ASN][1000 genomes]
rs9406537	0.82[ASN][1000 genomes]
rs9406539	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9406540	0.90[ASN][1000 genomes]
rs9406541	0.91[ASN][1000 genomes]
rs9406542	0.91[ASN][1000 genomes]
rs9406545	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9407648	0.91[ASN][1000 genomes]
rs9407649	0.91[ASN][1000 genomes]
rs9407650	0.90[ASN][1000 genomes]
rs9407651	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9407652	0.91[ASN][1000 genomes]
rs9407653	0.91[ASN][1000 genomes]
rs9407654	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9407655	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9407656	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9407657	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9407658	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9407661	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9407662	0.98[ASN][1000 genomes]
rs9407669	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv892632	chr9:15590116-15869845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv892635	chr9:15731775-15876507	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv528964	chr9:15760822-15875162	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv892636	chr9:15794858-15876507	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv613666	chr9:15823667-15875162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv613667	chr9:15823667-15876507	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15830200-15857200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15835000-15846600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:15835200-15843400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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