Variant report

Variant	rs11023987
Chromosome Location	chr11:16586746-16586747
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10766329	0.85[ASN][1000 genomes]
rs10766331	1.00[ASN][1000 genomes]
rs10832622	0.84[ASN][1000 genomes]
rs10832627	0.85[ASN][1000 genomes]
rs10832628	0.94[ASN][1000 genomes]
rs10832629	0.94[ASN][1000 genomes]
rs10832635	0.99[ASN][1000 genomes]
rs10832637	0.99[ASN][1000 genomes]
rs10832639	0.99[ASN][1000 genomes]
rs10832640	1.00[ASN][1000 genomes]
rs10832642	1.00[ASN][1000 genomes]
rs10832643	1.00[ASN][1000 genomes]
rs10832646	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11023959	0.81[ASN][1000 genomes]
rs11023960	0.81[ASN][1000 genomes]
rs11023962	0.82[ASN][1000 genomes]
rs11023981	1.00[ASN][1000 genomes]
rs11023988	1.00[ASN][1000 genomes]
rs11529132	0.85[ASN][1000 genomes]
rs11529582	0.85[ASN][1000 genomes]
rs12270317	0.91[ASN][1000 genomes]
rs12271656	0.85[ASN][1000 genomes]
rs12276256	0.85[ASN][1000 genomes]
rs12283896	0.97[ASN][1000 genomes]
rs12289091	0.92[ASN][1000 genomes]
rs12289093	0.89[ASN][1000 genomes]
rs12786848	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34138863	0.81[ASN][1000 genomes]
rs34840028	1.00[ASN][1000 genomes]
rs35223308	0.83[ASN][1000 genomes]
rs4359170	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4447142	0.83[EUR][1000 genomes]
rs4492775	0.85[ASN][1000 genomes]
rs4511252	1.00[ASN][1000 genomes]
rs4525190	0.99[ASN][1000 genomes]
rs4536174	0.99[ASN][1000 genomes]
rs4578351	0.92[ASN][1000 genomes]
rs4603269	1.00[ASN][1000 genomes]
rs57248274	0.81[ASN][1000 genomes]
rs60439454	0.84[ASN][1000 genomes]
rs6486296	0.91[ASN][1000 genomes]
rs6486298	0.92[ASN][1000 genomes]
rs7117636	0.85[ASN][1000 genomes]
rs7126577	0.83[ASN][1000 genomes]
rs7129286	0.99[ASN][1000 genomes]
rs7924787	1.00[ASN][1000 genomes]
rs7935041	0.92[ASN][1000 genomes]
rs7937139	1.00[ASN][1000 genomes]
rs7942856	0.98[ASN][1000 genomes]
rs7943712	0.97[ASN][1000 genomes]
rs7945295	1.00[ASN][1000 genomes]
rs7945898	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv983173	chr11:16581343-16600284	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16573000-16594600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:16583800-16594000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:16584400-16593000	Weak transcription	Psoas Muscle	Psoas
4	chr11:16584400-16605600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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