Variant report

Variant	rs7704835
Chromosome Location	chr5:91161313-91161314
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10037971	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10039744	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10041328	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10042631	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10058325	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10063941	0.82[EUR][1000 genomes]
rs10072620	0.88[ASN][1000 genomes]
rs1019740	0.82[EUR][1000 genomes]
rs1019741	0.82[EUR][1000 genomes]
rs10942647	0.92[ASN][1000 genomes]
rs10942648	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10942649	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10942653	0.80[EUR][1000 genomes]
rs12516680	0.88[ASN][1000 genomes]
rs12655533	0.80[EUR][1000 genomes]
rs1366131	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1366132	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1427954	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1560046	0.88[ASN][1000 genomes]
rs1863951	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1946452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2114980	0.82[EUR][1000 genomes]
rs2195277	0.82[EUR][1000 genomes]
rs58022129	0.92[ASN][1000 genomes]
rs62368361	0.91[ASN][1000 genomes]
rs62368362	0.88[ASN][1000 genomes]
rs62368363	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6880158	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7703024	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7707917	0.91[ASN][1000 genomes]
rs7710172	0.82[EUR][1000 genomes]
rs7716624	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7716965	0.82[EUR][1000 genomes]
rs7719384	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7721652	0.80[EUR][1000 genomes]
rs7722618	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7730541	0.82[EUR][1000 genomes]
rs7736013	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7736802	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs825389	0.80[EUR][1000 genomes]
rs825397	0.80[EUR][1000 genomes]
rs825398	0.80[EUR][1000 genomes]
rs825399	0.80[EUR][1000 genomes]
rs9293589	0.88[ASN][1000 genomes]
rs9293590	0.88[ASN][1000 genomes]
rs9293591	0.88[ASN][1000 genomes]
rs9293593	0.82[EUR][1000 genomes]
rs953550	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs979446	0.91[ASN][1000 genomes]
rs979447	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882370	chr5:90986181-91287437	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv882372	chr5:91018052-91221647	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1017504	chr5:91092920-91178854	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv830396	chr5:91121355-91343236	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv882373	chr5:91144658-91275313	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv882374	chr5:91144658-91287437	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv882375	chr5:91144658-91383848	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91160400-91162400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr5:91160400-91162600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:91160400-91163200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr5:91160600-91161800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:91160600-91162000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:91160600-91162000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr5:91160600-91162400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:91160600-91162400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:91160600-91162600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:91160600-91162600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:91161000-91161800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:91161000-91161800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:91161000-91161800	Enhancers	Fetal Lung	lung
14	chr5:91161000-91162400	Enhancers	HUES6 Cell Line	embryonic stem cell

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