Variant report

Variant	rs1934978
Chromosome Location	chr10:96813399-96813400
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1058932	0.89[ASN][1000 genomes]
rs10882517	0.94[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10882518	0.89[ASN][1000 genomes]
rs10882520	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882525	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1113129	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11188147	0.94[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11188149	0.90[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11188156	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11572101	0.92[ASN][1000 genomes]
rs11572124	0.92[ASN][1000 genomes]
rs11572133	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12246157	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12571878	0.90[ASN][1000 genomes]
rs12773510	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs13313110	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs13313124	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1341158	0.92[ASN][1000 genomes]
rs1341159	0.94[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1341162	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1578436	0.94[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1891070	0.95[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1934951	0.89[ASN][1000 genomes]
rs1934977	0.92[ASN][1000 genomes]
rs1934980	0.92[ASN][1000 genomes]
rs2148551	0.92[ASN][1000 genomes]
rs36180793	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3752988	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7073968	0.94[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7917837	0.90[ASN][1000 genomes]
rs947172	0.91[ASN][1000 genomes]
rs947173	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9702453	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1035409	chr10:96495177-96832057	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1050544	chr10:96766934-96814689	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv1044182	chr10:96783996-96814689	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	esv2761618	chr10:96784008-96814689	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats	TF binding region CpG island lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
7	nsv467436	chr10:96805371-96862286	Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
8	nsv551964	chr10:96805371-96862286	ZNF genes & repeats Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1934978	CYP2C19	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96805400-96823600	Weak transcription	Pancreas	Pancrea
2	chr10:96812600-96813800	Strong transcription	Liver	Liver

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