Variant report

Variant	rs10109048
Chromosome Location	chr8:119461424-119461425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10094604	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10096317	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10101386	0.84[ASN][1000 genomes]
rs10108907	0.89[ASN][1000 genomes]
rs10282819	0.89[ASN][1000 genomes]
rs10283133	0.89[ASN][1000 genomes]
rs10955883	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10955884	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10955885	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10955886	0.89[ASN][1000 genomes]
rs10955887	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11773916	0.83[ASN][1000 genomes]
rs11773953	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11777111	0.83[ASN][1000 genomes]
rs11782499	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11784091	0.83[ASN][1000 genomes]
rs11784138	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12155913	0.82[ASN][1000 genomes]
rs12156430	0.83[ASN][1000 genomes]
rs12544750	0.91[ASN][1000 genomes]
rs12675551	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12677506	0.91[ASN][1000 genomes]
rs12679343	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12679866	0.85[ASN][1000 genomes]
rs12681581	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12681600	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13248112	0.83[ASN][1000 genomes]
rs13251354	0.82[ASN][1000 genomes]
rs13251719	0.81[ASN][1000 genomes]
rs13253470	0.82[ASN][1000 genomes]
rs13253764	0.82[ASN][1000 genomes]
rs13255144	0.91[ASN][1000 genomes]
rs13260753	0.82[ASN][1000 genomes]
rs13263320	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13265657	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4075614	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4128894	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4242578	0.82[ASN][1000 genomes]
rs4242579	0.83[ASN][1000 genomes]
rs4242580	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4375037	0.84[ASN][1000 genomes]
rs4443692	0.88[ASN][1000 genomes]
rs4492409	0.85[ASN][1000 genomes]
rs4493938	0.90[ASN][1000 genomes]
rs4548208	0.84[ASN][1000 genomes]
rs4601348	0.84[ASN][1000 genomes]
rs4626637	0.84[ASN][1000 genomes]
rs4629902	0.85[ASN][1000 genomes]
rs4631494	0.84[ASN][1000 genomes]
rs4876416	0.85[ASN][1000 genomes]
rs4876417	0.91[ASN][1000 genomes]
rs4876833	0.81[ASN][1000 genomes]
rs4876835	0.85[ASN][1000 genomes]
rs4876836	0.91[ASN][1000 genomes]
rs4876837	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4876838	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4876839	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4876840	0.91[ASN][1000 genomes]
rs4876841	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4876842	0.91[ASN][1000 genomes]
rs4876845	0.91[ASN][1000 genomes]
rs59298785	0.84[ASN][1000 genomes]
rs61636365	0.84[ASN][1000 genomes]
rs62533427	0.84[ASN][1000 genomes]
rs6469747	0.90[ASN][1000 genomes]
rs6981538	0.90[ASN][1000 genomes]
rs6982369	0.90[ASN][1000 genomes]
rs6983068	0.91[ASN][1000 genomes]
rs6985503	0.89[ASN][1000 genomes]
rs7012582	0.89[ASN][1000 genomes]
rs7812733	0.85[ASN][1000 genomes]
rs7812880	0.85[ASN][1000 genomes]
rs7813395	0.85[ASN][1000 genomes]
rs7825963	0.91[ASN][1000 genomes]
rs7826257	0.91[ASN][1000 genomes]
rs7826375	0.91[ASN][1000 genomes]
rs7826888	0.87[ASN][1000 genomes]
rs7830347	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7830423	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7831361	0.85[ASN][1000 genomes]
rs7831501	0.85[ASN][1000 genomes]
rs7835295	0.90[ASN][1000 genomes]
rs7838464	0.84[ASN][1000 genomes]
rs7846218	0.89[ASN][1000 genomes]
rs9297587	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9642841	0.85[ASN][1000 genomes]
rs9643128	0.85[ASN][1000 genomes]
rs9643129	0.85[ASN][1000 genomes]
rs9643130	0.85[ASN][1000 genomes]
rs9656927	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612047	chr8:118939094-119468609	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1032681	chr8:119153316-119609948	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv539737	chr8:119153316-119609948	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv831443	chr8:119390590-119590662	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 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	chr8:119449200-119475400	Weak transcription	Gastric	stomach
2	chr8:119453200-119462400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:119456400-119462200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:119457400-119462200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:119457400-119462200	Weak transcription	Fetal Heart	heart

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