Variant report

Variant	rs73682605
Chromosome Location	chr8:62791679-62791680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLVS1-3	chr8:62791441-62792336	ENSG00000254119

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10088053	1.00[ASN][1000 genomes]
rs16928033	1.00[ASN][1000 genomes]
rs16928035	1.00[ASN][1000 genomes]
rs28793274	1.00[ASN][1000 genomes]
rs56016636	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56125512	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56235963	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57344387	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58080416	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58710029	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58960042	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59120662	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60520860	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471975	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66667350	1.00[ASN][1000 genomes]
rs67870277	1.00[ASN][1000 genomes]
rs6991008	1.00[ASN][1000 genomes]
rs7008718	1.00[ASN][1000 genomes]
rs7012432	1.00[ASN][1000 genomes]
rs7012678	1.00[ASN][1000 genomes]
rs73255128	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73255147	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73255155	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73255157	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73682603	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73685132	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73685158	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73685159	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2761430	chr8:62517980-62873803	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1015216	chr8:62517980-62873803	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv611427	chr8:62733267-62848952	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv831338	chr8:62736394-62913048	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1032414	chr8:62789246-62861376	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62789800-62791800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:62790000-62792200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:62790600-62794000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr8:62790600-62794200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr8:62790600-62795000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr8:62791200-62792200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr8:62791600-62794400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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