Variant report

Variant	rs536914
Chromosome Location	chr13:64422939-64422940
allele	C/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	CEBPB	chr13:64422818-64422949	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
ENSG00000219926	TF binding region

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1039005	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs10507702	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12427493	0.91[ASN][1000 genomes]
rs12428552	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12428562	0.91[ASN][1000 genomes]
rs12429666	0.97[ASN][1000 genomes]
rs1591483	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1809671	1.00[ASN][1000 genomes]
rs1809672	1.00[ASN][1000 genomes]
rs1809673	1.00[ASN][1000 genomes]
rs1809674	1.00[ASN][1000 genomes]
rs1809675	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1826133	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1932376	0.91[ASN][1000 genomes]
rs2050477	1.00[ASN][1000 genomes]
rs2635991	0.91[ASN][1000 genomes]
rs275913	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs275932	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2807121	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3866531	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4883724	0.94[ASN][1000 genomes]
rs4883725	0.94[ASN][1000 genomes]
rs4884521	1.00[ASN][1000 genomes]
rs496097	0.90[AFR][1000 genomes]
rs498958	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs506695	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs556065	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs563389	0.91[ASN][1000 genomes]
rs56890343	0.91[ASN][1000 genomes]
rs589325	0.91[ASN][1000 genomes]
rs590719	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7335738	1.00[ASN][1000 genomes]
rs74087239	0.91[ASN][1000 genomes]
rs74087241	0.88[ASN][1000 genomes]
rs7998209	0.91[ASN][1000 genomes]
rs824761	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9564108	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9564124	0.97[ASN][1000 genomes]
rs9571054	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9571073	1.00[ASN][1000 genomes]
rs9571074	1.00[ASN][1000 genomes]
rs9571078	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042265	chr13:63945130-64471230	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv2756457	chr13:64244499-64497199	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv870276	chr13:64287557-64424570	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv900323	chr13:64290980-64513203	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2754198	chr13:64303507-64424251	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1036453	chr13:64329019-64430033	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv900331	chr13:64346536-64450375	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv832633	chr13:64385305-64521487	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1046038	chr13:64405310-64500692	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv976127	chr13:64407800-64424929	ZNF genes & repeats Enhancers Weak transcription	TF binding region CpG island lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv900332	chr13:64411616-64856866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	esv2829984	chr13:64412839-64517258	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv561964	chr13:64412839-64967458	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv1044946	chr13:64419179-64937470	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64422200-64423000	Enhancers	Fetal Lung	lung
2	chr13:64422400-64423200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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