Variant report

Variant	rs36005639
Chromosome Location	chr11:9121518-9121519
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11042260	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1136330	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11600093	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11600994	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11601190	0.82[EUR][1000 genomes]
rs11601229	0.85[EUR][1000 genomes]
rs11601340	0.87[AMR][1000 genomes]
rs11601383	0.87[AMR][1000 genomes]
rs11603759	0.86[AMR][1000 genomes]
rs11604054	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11604121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11604198	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11604607	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11605358	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11606260	0.97[EUR][1000 genomes]
rs11606740	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11606969	0.82[EUR][1000 genomes]
rs11607790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11608223	1.00[AFR][1000 genomes]
rs16906708	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16914802	0.95[EUR][1000 genomes]
rs4910036	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4910038	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4910039	0.87[AMR][1000 genomes]
rs4910441	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4910449	1.00[AFR][1000 genomes]
rs55723890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55741313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55980718	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55989000	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55994936	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56002897	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56065481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56081129	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56292930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7394938	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7395168	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7395453	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7395754	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7396336	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7396512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs956516	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413845	chr11:8887279-9285127	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	esv33264	chr11:9007612-9311131	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv896985	chr11:9013002-9152463	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv467704	chr11:9059192-9125301	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
5	nsv553454	chr11:9059192-9125301	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9113600-9159800	Weak transcription	Right Ventricle	heart
2	chr11:9114200-9122000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:9114200-9136200	Weak transcription	Fetal Heart	heart
4	chr11:9115000-9141800	Weak transcription	HSMM	muscle
5	chr11:9115200-9134400	Weak transcription	Fetal Stomach	stomach
6	chr11:9115800-9121800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:9119000-9124800	Weak transcription	Pancreas	Pancrea
8	chr11:9120600-9121800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:9121200-9121800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:9121200-9121800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr11:9121200-9121800	Flanking Active TSS	K562	blood
12	chr11:9121400-9121800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr11:9121400-9121800	Enhancers	Brain Substantia Nigra	brain

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