Variant report

Variant	rs11024987
Chromosome Location	chr11:19111968-19111969
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10444252	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10444253	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10444255	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10500837	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024985	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11024986	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11024988	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11024989	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024990	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024991	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024992	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024993	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024994	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024995	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024996	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024998	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11024999	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025002	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025004	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025005	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025006	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025007	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11025008	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16936115	0.80[AFR][1000 genomes]
rs16936140	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs59840223	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72889769	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72889773	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72889781	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72889786	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72889799	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72889802	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72891506	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72891507	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72891510	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72907780	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72907782	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72907784	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72907786	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9299952	0.88[CEU][hapmap];0.96[AMR][1000 genomes];0.99[EUR][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	nsv1040805	chr11:19037871-19892803	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv540957	chr11:19037871-19892803	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 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	chr11:19108200-19113400	Enhancers	HUVEC	blood vessel
2	chr11:19110000-19112000	Weak transcription	NH-A	brain
3	chr11:19110000-19115400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:19110400-19112800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:19110600-19112000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:19110800-19112000	Enhancers	NHEK	skin
7	chr11:19111800-19112200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:19111800-19112600	Enhancers	Esophagus	oesophagus

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