Variant report

Variant	rs10769909
Chromosome Location	chr11:8491597-8491598
allele	C/T
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]
rs10437594	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10437663	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10743077	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10769912	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10769913	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840046	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840048	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840049	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840053	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10840054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840059	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840068	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840069	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840071	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840073	1.00[ASN][1000 genomes]
rs10840074	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10840075	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840076	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840078	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840082	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10840086	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840088	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041922	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11041923	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11041928	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041936	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041937	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041938	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041942	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041956	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041957	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041959	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11041961	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041984	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041987	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041988	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041989	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041992	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11042001	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11042005	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11042009	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11042010	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11042027	0.87[EUR][1000 genomes]
rs11512437	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11517716	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12281197	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12282087	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12282398	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12283443	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12361165	1.00[ASN][1000 genomes]
rs12362755	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12364516	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12364713	0.93[ASN][1000 genomes]
rs12365973	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418359	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418525	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12419725	1.00[EUR][1000 genomes]
rs12422205	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12573963	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12575045	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1867812	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2100066	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34381273	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4450173	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4627069	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58364522	1.00[ASN][1000 genomes]
rs59084068	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7102605	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7108120	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7108379	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7127840	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs726008	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73403636	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408023	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73408025	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7941120	0.81[ASN][1000 genomes]
rs9737172	0.93[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	esv2751035	chr11:8431654-8685451	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv32551	chr11:8457023-8534642	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8464600-8495800	Weak transcription	Fetal Heart	heart
2	chr11:8488200-8491600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:8488200-8492600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:8490000-8497600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:8490000-8497600	Weak transcription	Ovary	ovary
6	chr11:8491000-8492400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:8491200-8492600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:8491400-8492200	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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