Variant report

Variant	rs10828961
Chromosome Location	chr10:26478943-26478944
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10508711	0.81[ASN][1000 genomes]
rs10508712	0.86[ASN][1000 genomes]
rs10764599	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10828951	0.83[ASN][1000 genomes]
rs10828954	0.88[ASN][1000 genomes]
rs10828957	0.90[ASN][1000 genomes]
rs10828958	0.89[ASN][1000 genomes]
rs10828962	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11014960	0.85[ASN][1000 genomes]
rs11014983	0.95[ASN][1000 genomes]
rs11599503	0.83[ASN][1000 genomes]
rs12219979	0.90[ASN][1000 genomes]
rs12269307	0.98[ASN][1000 genomes]
rs12764197	0.94[ASN][1000 genomes]
rs12775931	0.82[ASN][1000 genomes]
rs12781541	0.90[ASN][1000 genomes]
rs1361713	0.94[ASN][1000 genomes]
rs17752077	0.90[ASN][1000 genomes]
rs17752353	0.98[ASN][1000 genomes]
rs1935483	0.89[ASN][1000 genomes]
rs2000255	0.94[ASN][1000 genomes]
rs2051084	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2275727	0.85[ASN][1000 genomes]
rs2887177	0.95[ASN][1000 genomes]
rs34240977	0.98[ASN][1000 genomes]
rs34966498	0.93[ASN][1000 genomes]
rs3737316	0.95[ASN][1000 genomes]
rs3817416	0.84[ASN][1000 genomes]
rs3818957	0.90[ASN][1000 genomes]
rs4526683	0.98[ASN][1000 genomes]
rs4747546	0.94[ASN][1000 genomes]
rs4749092	0.85[ASN][1000 genomes]
rs4749094	0.94[ASN][1000 genomes]
rs4749098	0.94[ASN][1000 genomes]
rs6482535	0.98[ASN][1000 genomes]
rs7083144	0.97[ASN][1000 genomes]
rs7083433	0.87[ASN][1000 genomes]
rs7905083	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7908081	0.98[ASN][1000 genomes]
rs7915636	0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26474000-26491000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26478400-26483000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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