Variant report

Variant	rs2692182
Chromosome Location	chr7:147002373-147002374
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs1021008	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10248220	1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[YRI][hapmap]
rs10261539	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[YRI][hapmap]
rs10261547	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs10808044	0.83[CHB][hapmap]
rs12531764	0.83[CHB][hapmap]
rs12534978	1.00[CEU][hapmap];0.88[YRI][hapmap]
rs1383011	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs1404703	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs1404706	0.89[ASN][1000 genomes]
rs1404707	0.83[CHB][hapmap]
rs1479837	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs1479838	0.83[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs1479839	0.89[ASN][1000 genomes]
rs1479840	0.84[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs1525208	0.89[ASN][1000 genomes]
rs1525209	0.83[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs1525210	0.89[ASN][1000 genomes]
rs1525215	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[YRI][hapmap]
rs1525216	0.82[CHB][hapmap]
rs1917600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2373026	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2620439	0.83[CHB][hapmap]
rs2620440	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs2620441	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs2620443	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2620446	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs2620447	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2620450	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2620452	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2620454	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2620455	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2620460	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs2620464	0.94[JPT][hapmap]
rs2620465	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs2620467	0.94[JPT][hapmap]
rs2692139	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs2692140	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2692141	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs2692143	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2692144	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2692145	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2692146	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2692149	0.94[JPT][hapmap]
rs2692150	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2692151	0.81[CHB][hapmap];0.93[JPT][hapmap]
rs2692154	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2692157	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2692158	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs2692162	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs2692163	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs2692164	0.83[CHB][hapmap];0.93[JPT][hapmap]
rs2692168	0.83[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692170	0.89[ASN][1000 genomes]
rs2692173	0.89[ASN][1000 genomes]
rs2692174	0.89[ASN][1000 genomes]
rs2692175	0.85[ASN][1000 genomes]
rs2692176	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2692177	0.89[ASN][1000 genomes]
rs2692178	0.89[ASN][1000 genomes]
rs2692179	0.83[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692180	0.84[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2692183	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs2692185	0.83[JPT][hapmap]
rs4269450	0.94[JPT][hapmap]
rs6974852	1.00[CEU][hapmap];0.89[YRI][hapmap]
rs728720	0.83[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs899612	0.94[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs899613	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs899614	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs899615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs899616	0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs9969115	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs9969256	0.83[CHB][hapmap];0.94[JPT][hapmap]

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	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv889396	chr7:146854133-147035067	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1026360	chr7:146988190-147012081	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv1033398	chr7:146989035-147101573	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
7	nsv1029946	chr7:146993413-147021947	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv465192	chr7:147001077-147086045	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
9	nsv608943	chr7:147001077-147086045	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146996400-147008000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:147000600-147002600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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