Variant report

Variant	rs62267195
Chromosome Location	chr3:97951361-97951362
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CUX1	chr3:97951097-97951764	GM12878	blood:	n/a	n/a
2	ZNF384	chr3:97950860-97952665	GM12878	blood:	n/a	n/a
3	EBF1	chr3:97950253-97951851	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000251088	TF binding region

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10511165	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12629487	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1497533	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1497534	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1497535	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16839368	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16839394	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16839408	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16839424	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55642832	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55655921	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55701454	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55844177	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55956513	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56318537	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56329277	1.00[ASN][1000 genomes]
rs56408745	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57715149	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60447690	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267180	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62267181	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62267182	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62267183	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267184	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267185	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267186	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267187	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267188	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267189	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267196	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62267222	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62267224	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62267807	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62268890	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62268895	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62269763	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62269764	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62269765	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6439692	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6771829	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6771947	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786518	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786750	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795155	0.97[ASN][1000 genomes]
rs72929022	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73853705	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73853707	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73853708	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73853747	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73853752	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73855832	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7627018	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7629122	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7636916	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869347	chr3:97742604-98051633	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv877209	chr3:97806616-98049409	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv963576	chr3:97825434-98041343	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv834773	chr3:97855362-98043888	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv877210	chr3:97866177-97992964	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv432462	chr3:97918267-98001710	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv877211	chr3:97919363-97958280	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv591063	chr3:97924688-97958280	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv591064	chr3:97931105-97958280	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv877212	chr3:97931105-98033400	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv1004762	chr3:97935701-98000227	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv1008569	chr3:97937168-97983117	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv1009918	chr3:97946030-98155450	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97951200-97952800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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