Variant report

Variant	rs11041959
Chromosome Location	chr11:8547822-8547823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10437594	0.96[ASN][1000 genomes]
rs10437663	0.96[ASN][1000 genomes]
rs10743077	1.00[ASN][1000 genomes]
rs10769909	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10769912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10769913	1.00[ASN][1000 genomes]
rs10840046	0.90[ASN][1000 genomes]
rs10840048	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10840049	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10840053	1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10840054	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10840059	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10840068	1.00[ASN][1000 genomes]
rs10840069	1.00[ASN][1000 genomes]
rs10840071	1.00[ASN][1000 genomes]
rs10840073	1.00[ASN][1000 genomes]
rs10840074	0.93[ASN][1000 genomes]
rs10840075	0.90[ASN][1000 genomes]
rs10840076	0.90[ASN][1000 genomes]
rs10840078	0.90[ASN][1000 genomes]
rs10840082	0.90[ASN][1000 genomes]
rs10840086	1.00[ASN][1000 genomes]
rs10840088	1.00[ASN][1000 genomes]
rs11041922	0.90[ASN][1000 genomes]
rs11041923	0.90[ASN][1000 genomes]
rs11041928	1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11041936	1.00[ASN][1000 genomes]
rs11041937	1.00[ASN][1000 genomes]
rs11041938	1.00[ASN][1000 genomes]
rs11041942	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11041956	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11041957	1.00[ASN][1000 genomes]
rs11041961	1.00[ASN][1000 genomes]
rs11041984	0.93[ASN][1000 genomes]
rs11041987	0.93[ASN][1000 genomes]
rs11041988	0.93[ASN][1000 genomes]
rs11041989	0.93[ASN][1000 genomes]
rs11041992	0.93[ASN][1000 genomes]
rs11042001	0.90[ASN][1000 genomes]
rs11042005	0.90[ASN][1000 genomes]
rs11042009	0.87[ASN][1000 genomes]
rs11042010	0.96[ASN][1000 genomes]
rs11512437	1.00[ASN][1000 genomes]
rs11517716	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12281197	0.90[ASN][1000 genomes]
rs12282087	1.00[ASN][1000 genomes]
rs12282398	1.00[ASN][1000 genomes]
rs12283443	1.00[ASN][1000 genomes]
rs12361165	1.00[ASN][1000 genomes]
rs12362755	0.82[ASN][1000 genomes]
rs12364516	0.80[ASN][1000 genomes]
rs12364713	0.93[ASN][1000 genomes]
rs12365973	1.00[ASN][1000 genomes]
rs12418359	1.00[ASN][1000 genomes]
rs12418525	1.00[ASN][1000 genomes]
rs12422205	1.00[ASN][1000 genomes]
rs12573963	1.00[ASN][1000 genomes]
rs12575045	1.00[ASN][1000 genomes]
rs1867812	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2100066	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34381273	0.93[ASN][1000 genomes]
rs4450173	1.00[ASN][1000 genomes]
rs4627069	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs58364522	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59084068	0.90[ASN][1000 genomes]
rs7102605	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7108120	0.90[ASN][1000 genomes]
rs7108379	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7127840	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs726008	0.90[ASN][1000 genomes]
rs73403636	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73408023	1.00[ASN][1000 genomes]
rs73408025	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	nsv896983	chr11:8526643-8682465	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8545400-8549600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:8546000-8549600	Weak transcription	Fetal Heart	heart
3	chr11:8546400-8548600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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