Variant report

Variant	rs9787562
Chromosome Location	chr10:26252005-26252006
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10508711	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs10508712	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs1075611	0.83[ASN][1000 genomes]
rs10828939	0.89[ASN][1000 genomes]
rs10828941	0.86[ASN][1000 genomes]
rs10828944	0.81[ASN][1000 genomes]
rs10828949	0.88[CEU][hapmap];0.85[CHB][hapmap];0.91[JPT][hapmap]
rs10828950	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs10828951	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs10828958	0.81[CEU][hapmap];0.86[JPT][hapmap]
rs11014832	0.90[ASN][1000 genomes]
rs11014837	0.90[ASN][1000 genomes]
rs11014839	0.90[ASN][1000 genomes]
rs11014840	0.91[ASN][1000 genomes]
rs11014841	0.90[ASN][1000 genomes]
rs11014861	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11014917	0.87[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs11014919	0.91[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs11014930	0.83[CEU][hapmap];0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs11014953	0.82[CEU][hapmap];0.83[JPT][hapmap]
rs11014955	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs11014960	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs11527599	0.80[ASN][1000 genomes]
rs11594081	0.89[ASN][1000 genomes]
rs11596244	0.89[ASN][1000 genomes]
rs11596246	0.89[ASN][1000 genomes]
rs11596291	0.89[ASN][1000 genomes]
rs12413819	0.89[ASN][1000 genomes]
rs12415065	0.89[ASN][1000 genomes]
rs12415073	0.89[ASN][1000 genomes]
rs12415076	0.89[ASN][1000 genomes]
rs12571378	0.87[ASN][1000 genomes]
rs12573019	0.87[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs12763779	0.90[ASN][1000 genomes]
rs12764003	0.90[ASN][1000 genomes]
rs12765016	0.90[ASN][1000 genomes]
rs12765882	0.90[ASN][1000 genomes]
rs12766116	0.90[ASN][1000 genomes]
rs12766438	0.89[ASN][1000 genomes]
rs12766618	0.89[ASN][1000 genomes]
rs12766630	0.87[ASN][1000 genomes]
rs12767158	0.89[ASN][1000 genomes]
rs12770771	0.90[ASN][1000 genomes]
rs12774203	0.82[ASN][1000 genomes]
rs12781541	0.82[CEU][hapmap];0.85[JPT][hapmap]
rs12783838	0.86[ASN][1000 genomes]
rs1339807	0.90[ASN][1000 genomes]
rs1339811	0.87[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs1339819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17745419	0.89[ASN][1000 genomes]
rs17745431	0.89[ASN][1000 genomes]
rs17745449	0.89[ASN][1000 genomes]
rs17745497	0.89[ASN][1000 genomes]
rs17745521	0.89[ASN][1000 genomes]
rs17745539	0.89[ASN][1000 genomes]
rs17745639	0.90[ASN][1000 genomes]
rs17813027	0.89[ASN][1000 genomes]
rs17813033	0.89[ASN][1000 genomes]
rs17813057	0.89[ASN][1000 genomes]
rs17813069	0.89[ASN][1000 genomes]
rs17813093	0.89[ASN][1000 genomes]
rs17813099	0.89[ASN][1000 genomes]
rs17813111	0.89[ASN][1000 genomes]
rs17813147	0.89[ASN][1000 genomes]
rs1935483	0.82[CEU][hapmap];0.85[JPT][hapmap]
rs1996715	0.88[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs2014483	0.85[ASN][1000 genomes]
rs2176938	0.86[ASN][1000 genomes]
rs2275727	0.82[CEU][hapmap]
rs34003574	0.89[ASN][1000 genomes]
rs34041877	0.89[ASN][1000 genomes]
rs34084425	0.88[ASN][1000 genomes]
rs34131502	0.89[ASN][1000 genomes]
rs34233765	0.88[ASN][1000 genomes]
rs34393388	0.89[ASN][1000 genomes]
rs34397260	0.89[ASN][1000 genomes]
rs34482812	0.90[ASN][1000 genomes]
rs34527620	0.80[ASN][1000 genomes]
rs34610428	0.89[ASN][1000 genomes]
rs34613665	0.89[ASN][1000 genomes]
rs34697018	0.89[ASN][1000 genomes]
rs34776712	0.89[ASN][1000 genomes]
rs34828805	0.89[ASN][1000 genomes]
rs34992226	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35291419	0.88[ASN][1000 genomes]
rs35326670	0.89[ASN][1000 genomes]
rs35554988	0.89[ASN][1000 genomes]
rs35773819	0.83[ASN][1000 genomes]
rs35936738	0.89[ASN][1000 genomes]
rs35938978	0.89[ASN][1000 genomes]
rs35972702	0.80[ASN][1000 genomes]
rs3817416	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs3818957	0.82[CEU][hapmap];0.85[JPT][hapmap]
rs3824706	0.82[ASN][1000 genomes]
rs3887832	0.83[ASN][1000 genomes]
rs4749086	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4749090	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4749092	0.82[CEU][hapmap];0.85[JPT][hapmap]
rs61009371	0.89[ASN][1000 genomes]
rs6482518	0.90[ASN][1000 genomes]
rs66751834	0.89[ASN][1000 genomes]
rs67808306	0.89[ASN][1000 genomes]
rs68073810	0.89[ASN][1000 genomes]
rs7083239	0.91[ASN][1000 genomes]
rs71495490	0.89[ASN][1000 genomes]
rs71499369	0.89[ASN][1000 genomes]
rs71499370	0.89[ASN][1000 genomes]
rs71499375	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs731797	0.83[ASN][1000 genomes]
rs748602	0.89[ASN][1000 genomes]
rs748603	0.82[ASN][1000 genomes]
rs7896978	0.90[ASN][1000 genomes]
rs7897690	0.90[ASN][1000 genomes]
rs7909123	0.90[ASN][1000 genomes]
rs7913600	0.90[ASN][1000 genomes]
rs946689	0.87[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	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

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26244200-26254400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:26248000-26252400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:26249800-26252800	Enhancers	Brain Germinal Matrix	brain
4	chr10:26250800-26261200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:26252000-26252400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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