Variant report

Variant	rs72784580
Chromosome Location	chr10:45800760-45800761
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10159580	0.92[EUR][1000 genomes]
rs10508894	1.00[AFR][1000 genomes]
rs10793613	0.92[EUR][1000 genomes]
rs10900195	0.92[EUR][1000 genomes]
rs10900200	0.92[EUR][1000 genomes]
rs10900209	0.81[EUR][1000 genomes]
rs11239402	0.90[AFR][1000 genomes]
rs11239409	0.90[AFR][1000 genomes]
rs11239420	1.00[AFR][1000 genomes]
rs11239423	1.00[AFR][1000 genomes]
rs11239427	1.00[AFR][1000 genomes]
rs11239428	1.00[AFR][1000 genomes]
rs11239430	0.81[AFR][1000 genomes]
rs11239432	0.92[EUR][1000 genomes]
rs11239434	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239435	0.92[EUR][1000 genomes]
rs11239437	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11239452	0.89[EUR][1000 genomes]
rs11239480	0.81[EUR][1000 genomes]
rs11239482	0.81[EUR][1000 genomes]
rs11239496	0.82[EUR][1000 genomes]
rs11522530	0.90[AFR][1000 genomes]
rs11522532	0.89[EUR][1000 genomes]
rs11523407	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11523866	0.89[EUR][1000 genomes]
rs12250005	0.92[EUR][1000 genomes]
rs12256027	0.81[EUR][1000 genomes]
rs12268890	0.92[EUR][1000 genomes]
rs12355274	1.00[AFR][1000 genomes]
rs12357069	0.89[EUR][1000 genomes]
rs12358110	0.87[EUR][1000 genomes]
rs12359547	0.81[EUR][1000 genomes]
rs12359672	1.00[AFR][1000 genomes]
rs1529828	0.87[EUR][1000 genomes]
rs1529829	0.87[EUR][1000 genomes]
rs17443340	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17521948	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1968475	0.86[EUR][1000 genomes]
rs28570111	0.88[EUR][1000 genomes]
rs28688874	0.89[EUR][1000 genomes]
rs2871740	0.81[EUR][1000 genomes]
rs55963543	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7085353	0.92[EUR][1000 genomes]
rs72784536	0.90[AFR][1000 genomes]
rs72784538	0.90[AFR][1000 genomes]
rs72784571	1.00[AFR][1000 genomes]
rs72786508	0.89[EUR][1000 genomes]
rs72788095	0.87[EUR][1000 genomes]
rs72788096	0.87[EUR][1000 genomes]
rs72788101	0.81[EUR][1000 genomes]
rs72788102	0.81[EUR][1000 genomes]
rs72789705	0.81[EUR][1000 genomes]
rs72789735	0.82[EUR][1000 genomes]
rs9664826	0.90[EUR][1000 genomes]
rs9733175	0.90[EUR][1000 genomes]
rs9733444	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv895105	chr10:45636867-45928822	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
3	nsv430166	chr10:45668894-46148794	Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv993428	chr10:45742877-46224333	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs72784580	OR13A1	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45798600-45803800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:45798600-45804000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr10:45799200-45801600	Weak transcription	K562	blood

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