Variant report

Variant	rs62192812
Chromosome Location	chr2:208939383-208939384
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10192860	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10497895	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10932224	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12464255	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12465052	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12470702	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13428099	0.92[EUR][1000 genomes]
rs16840403	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17538061	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17538138	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2362787	0.89[EUR][1000 genomes]
rs57709782	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs60335988	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62192772	0.87[EUR][1000 genomes]
rs62192773	0.87[EUR][1000 genomes]
rs62192790	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62192791	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62192814	0.96[EUR][1000 genomes]
rs62192815	0.96[EUR][1000 genomes]
rs62192816	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62192818	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72981543	0.92[EUR][1000 genomes]
rs72984907	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72984917	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72984926	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72984930	0.95[EUR][1000 genomes]
rs72984932	0.95[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	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv875743	chr2:208688648-208940023	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	esv2760541	chr2:208936949-208945639	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv519691	chr2:208938866-208940023	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 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	chr2:208938800-208939800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr2:208939200-208939800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr2:208939200-208940000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:208939200-208940000	Enhancers	Primary neutrophils fromperipheralblood	blood

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