Variant report

Variant	rs9576178
Chromosome Location	chr13:37679776-37679777
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1009963	0.89[ASN][1000 genomes]
rs11147624	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11147625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11147626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11147627	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11147629	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11147630	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11147632	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11620134	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1199995	0.93[ASN][1000 genomes]
rs1199996	0.93[ASN][1000 genomes]
rs12583685	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12584417	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12585998	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1336754	0.97[AFR][1000 genomes]
rs1336762	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1764480	0.91[ASN][1000 genomes]
rs1781669	0.94[ASN][1000 genomes]
rs1781670	0.94[ASN][1000 genomes]
rs1856028	0.97[AFR][1000 genomes]
rs1856029	0.92[ASN][1000 genomes]
rs1937757	0.87[AFR][1000 genomes]
rs2078022	0.86[JPT][hapmap]
rs2243710	0.86[JPT][hapmap]
rs2323396	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2670061	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3818380	0.86[JPT][hapmap]
rs3852618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3852619	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3852620	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3864999	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3888918	0.92[ASN][1000 genomes]
rs3904095	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3904755	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3914300	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4054546	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4485226	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943440	0.86[JPT][hapmap]
rs6563510	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6563511	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7327617	0.94[ASN][1000 genomes]
rs7335490	0.93[AFR][1000 genomes]
rs7981360	0.93[ASN][1000 genomes]
rs7996099	0.88[AFR][1000 genomes]
rs7996605	0.93[ASN][1000 genomes]
rs7996662	0.93[ASN][1000 genomes]
rs8000946	0.86[JPT][hapmap]
rs8002580	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8003010	0.93[ASN][1000 genomes]
rs945632	0.90[AFR][1000 genomes]
rs954370	0.86[JPT][hapmap]
rs9547711	0.86[JPT][hapmap]
rs9547713	0.86[JPT][hapmap]
rs9566176	0.82[AFR][1000 genomes]
rs9566177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9566178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9566183	0.94[ASN][1000 genomes]
rs9566184	0.94[ASN][1000 genomes]
rs9566185	0.93[ASN][1000 genomes]
rs9566186	0.93[ASN][1000 genomes]
rs9576151	0.86[JPT][hapmap]
rs9576167	0.85[JPT][hapmap]
rs9576172	0.82[AFR][1000 genomes]
rs9576173	0.83[AFR][1000 genomes]
rs9576175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576176	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576177	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9576180	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9576181	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576183	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9576184	1.00[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs9576185	0.82[ASN][1000 genomes]
rs9576186	0.93[ASN][1000 genomes]
rs9576187	0.93[ASN][1000 genomes]
rs9603126	0.86[JPT][hapmap]
rs9603139	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv826612	chr13:37678673-37680292	ZNF genes & repeats Weak transcription Enhancers Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37673600-37680800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:37677000-37680400	Weak transcription	Colon Smooth Muscle	Colon
3	chr13:37677200-37680200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr13:37677200-37680400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:37677200-37680400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr13:37677400-37680600	Weak transcription	HSMMtube	muscle
7	chr13:37677800-37682200	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr13:37678600-37680400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:37679200-37679800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:37679200-37679800	ZNF genes & repeats	Fetal Stomach	stomach
11	chr13:37679400-37679800	ZNF genes & repeats	Spleen	Spleen

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