Variant report

Variant	rs9561392
Chromosome Location	chr13:87638722-87638723
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11620198	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12583156	0.96[EUR][1000 genomes]
rs12584162	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12585485	0.96[EUR][1000 genomes]
rs12585659	0.96[EUR][1000 genomes]
rs2992715	0.93[EUR][1000 genomes]
rs35199018	0.93[EUR][1000 genomes]
rs4287428	0.93[EUR][1000 genomes]
rs4309266	0.92[EUR][1000 genomes]
rs4366593	0.93[EUR][1000 genomes]
rs4466948	0.92[EUR][1000 genomes]
rs4495988	0.93[EUR][1000 genomes]
rs4564442	0.92[EUR][1000 genomes]
rs61970701	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61970702	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61970728	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61973089	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61973370	0.93[EUR][1000 genomes]
rs7324982	0.89[EUR][1000 genomes]
rs7334147	0.92[EUR][1000 genomes]
rs7985959	0.93[EUR][1000 genomes]
rs7986098	0.93[EUR][1000 genomes]
rs7995182	0.96[EUR][1000 genomes]
rs7996680	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9556136	0.93[EUR][1000 genomes]
rs9556142	0.91[EUR][1000 genomes]
rs9556143	0.92[EUR][1000 genomes]
rs9556144	0.96[EUR][1000 genomes]
rs9556145	0.96[EUR][1000 genomes]
rs9556174	0.96[EUR][1000 genomes]
rs9556192	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9556199	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9556349	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9560921	0.96[EUR][1000 genomes]
rs9560937	0.96[EUR][1000 genomes]
rs9561005	0.96[EUR][1000 genomes]
rs9561008	0.96[EUR][1000 genomes]
rs9561009	0.96[EUR][1000 genomes]
rs9561066	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9561095	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9561105	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9561108	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9561109	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9561122	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9561214	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9561217	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9561221	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9561257	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9561259	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9561261	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9561404	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9561408	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];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	nsv900763	chr13:87073397-87658986	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv562621	chr13:87192747-87927450	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv900775	chr13:87311967-87658986	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3439251	chr13:87398732-87699077	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv900778	chr13:87407377-87658986	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv900779	chr13:87443524-87658986	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1046278	chr13:87461244-87712231	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1044991	chr13:87461244-87713936	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv900781	chr13:87492357-87658986	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv900782	chr13:87536247-87658986	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv832671	chr13:87539345-87707707	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv900783	chr13:87546157-87643970	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv900784	chr13:87546157-87647740	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv428607	chr13:87633567-87766875	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87637800-87639600	Enhancers	Liver	Liver
2	chr13:87638400-87639000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:87638400-87639000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:87638600-87639000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:87638600-87639400	Enhancers	HepG2	liver

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