Variant report

Variant	rs4389936
Chromosome Location	chr8:35326122-35326123
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10099855	0.83[AMR][1000 genomes]
rs10102863	0.83[AMR][1000 genomes]
rs10111986	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10112860	0.83[AMR][1000 genomes]
rs10503980	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12334629	0.83[AMR][1000 genomes]
rs12334687	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12541423	1.00[CEU][hapmap];0.87[JPT][hapmap]
rs12544168	0.80[ASN][1000 genomes]
rs12544701	0.83[AMR][1000 genomes]
rs12545517	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12546786	1.00[CEU][hapmap];0.87[JPT][hapmap]
rs12550037	1.00[CEU][hapmap];0.87[JPT][hapmap]
rs1371150	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1371154	0.80[ASN][1000 genomes]
rs1439149	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1439150	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1439159	0.83[AMR][1000 genomes]
rs16884019	0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs16884041	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs16884099	0.80[ASN][1000 genomes]
rs1837346	0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1837348	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2053340	0.80[ASN][1000 genomes]
rs2053342	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs41360948	0.84[CHB][hapmap];0.82[ASN][1000 genomes]
rs4237083	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4237084	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4302835	0.82[ASN][1000 genomes]
rs4361760	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4481589	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4529455	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4577954	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4579522	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739409	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739412	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4739414	0.80[ASN][1000 genomes]
rs4739415	0.80[ASN][1000 genomes]
rs58417870	0.80[ASN][1000 genomes]
rs59091238	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6988474	1.00[CEU][hapmap];0.87[JPT][hapmap]
rs6989128	0.80[ASN][1000 genomes]
rs6990731	0.80[ASN][1000 genomes]
rs6990960	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6992105	0.82[ASN][1000 genomes]
rs7001739	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7002810	1.00[CEU][hapmap];0.84[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs7002972	1.00[CEU][hapmap];0.84[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs7011885	0.82[ASN][1000 genomes]
rs7016526	0.80[ASN][1000 genomes]
rs73571880	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7829642	0.80[ASN][1000 genomes]
rs7833633	0.80[ASN][1000 genomes]
rs7841785	0.80[ASN][1000 genomes]
rs953345	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs953346	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs953347	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9656746	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs983270	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv520421	chr8:35155517-35479468	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1024397	chr8:35296922-35424277	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35319000-35334000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:35319000-35334200	Weak transcription	Fetal Brain Male	brain
3	chr8:35324000-35326600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr8:35324800-35326200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:35325800-35326200	Enhancers	HUES48 Cell Line	embryonic stem cell

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