Variant report

Variant	rs7992532
Chromosome Location	chr13:88709961-88709962
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1333794	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1333795	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1333796	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1333797	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1333801	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1529361	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1541772	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1541773	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1855390	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1855391	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1855392	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1855395	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2346339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2346340	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4142406	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4772584	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4772600	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4772625	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4772631	0.90[EUR][1000 genomes]
rs61959190	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7319127	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7999115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9284218	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9284219	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9300906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9300944	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9300946	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9514209	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9514240	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9514256	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9519209	0.82[EUR][1000 genomes]
rs9519267	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9519269	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9519309	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9519311	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9519321	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9519322	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9519323	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9519324	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9555037	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9558262	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9558263	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9558267	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9558268	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9558328	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9558329	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9558380	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9558381	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9558397	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9586474	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900790	chr13:88585928-88891870	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900791	chr13:88623302-88771495	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv900792	chr13:88623302-88871759	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr13:88707400-88711400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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