Variant report

Variant	rs11014812
Chromosome Location	chr10:26163735-26163736
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs11014814	0.95[ASN][1000 genomes]
rs11014832	0.81[EUR][1000 genomes]
rs11594081	0.81[EUR][1000 genomes]
rs11596244	0.81[EUR][1000 genomes]
rs11596246	0.81[EUR][1000 genomes]
rs11596291	0.81[EUR][1000 genomes]
rs12413819	0.81[EUR][1000 genomes]
rs12415065	0.81[EUR][1000 genomes]
rs12415073	0.81[EUR][1000 genomes]
rs12415076	0.81[EUR][1000 genomes]
rs12763779	0.81[EUR][1000 genomes]
rs12764003	0.81[EUR][1000 genomes]
rs12765882	0.81[EUR][1000 genomes]
rs12766116	0.81[EUR][1000 genomes]
rs12766438	0.85[EUR][1000 genomes]
rs12766618	0.85[EUR][1000 genomes]
rs12766630	0.85[EUR][1000 genomes]
rs12767158	0.85[EUR][1000 genomes]
rs12783838	0.84[EUR][1000 genomes]
rs12785219	0.80[EUR][1000 genomes]
rs17745419	0.85[EUR][1000 genomes]
rs17745431	0.85[EUR][1000 genomes]
rs17745449	0.85[EUR][1000 genomes]
rs17745497	0.81[EUR][1000 genomes]
rs17745521	0.81[EUR][1000 genomes]
rs17745539	0.81[EUR][1000 genomes]
rs17745639	0.81[EUR][1000 genomes]
rs17813027	0.85[EUR][1000 genomes]
rs17813033	0.85[EUR][1000 genomes]
rs17813057	0.85[EUR][1000 genomes]
rs17813069	0.81[EUR][1000 genomes]
rs17813093	0.81[EUR][1000 genomes]
rs17813099	0.81[EUR][1000 genomes]
rs17813111	0.81[EUR][1000 genomes]
rs17813147	0.81[EUR][1000 genomes]
rs2014483	0.82[EUR][1000 genomes]
rs34003574	0.81[EUR][1000 genomes]
rs34041877	0.85[EUR][1000 genomes]
rs34084425	0.85[EUR][1000 genomes]
rs34131502	0.81[EUR][1000 genomes]
rs34393388	0.81[EUR][1000 genomes]
rs34397260	0.81[EUR][1000 genomes]
rs34482812	0.81[EUR][1000 genomes]
rs34610428	0.81[EUR][1000 genomes]
rs34776712	0.81[EUR][1000 genomes]
rs34828805	0.81[EUR][1000 genomes]
rs35291419	0.85[EUR][1000 genomes]
rs35326670	0.81[EUR][1000 genomes]
rs35554988	0.81[EUR][1000 genomes]
rs35938978	0.85[EUR][1000 genomes]
rs61009371	0.85[EUR][1000 genomes]
rs6482518	0.81[EUR][1000 genomes]
rs66751834	0.81[EUR][1000 genomes]
rs67808306	0.81[EUR][1000 genomes]
rs68073810	0.81[EUR][1000 genomes]
rs71495490	0.81[EUR][1000 genomes]
rs71499369	0.81[EUR][1000 genomes]
rs71499370	0.81[EUR][1000 genomes]
rs748602	0.81[EUR][1000 genomes]
rs7896978	0.81[EUR][1000 genomes]
rs7897690	0.81[EUR][1000 genomes]
rs7909123	0.81[EUR][1000 genomes]
rs7913600	0.81[EUR][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	nsv894974	chr10:26028530-26322783	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1051756	chr10:26092320-26277478	Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3413743	chr10:26162546-26164444	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26163600-26164600	Enhancers	Pancreatic Islets	Pancreatic Islet

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