Variant report

Variant	rs8058598
Chromosome Location	chr16:31865194-31865195
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10871460	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11150650	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11150651	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12444740	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12599066	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12919368	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12924931	0.89[EUR][1000 genomes]
rs1827959	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1828131	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1857943	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2358778	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3843960	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3843961	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3850114	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3861268	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3861270	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3913868	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3913870	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3913871	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4026652	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4026654	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4402587	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4889517	0.89[EUR][1000 genomes]
rs4889518	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4889563	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4889565	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4889567	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4889568	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4889569	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6565290	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6565291	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7197804	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7200162	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7202831	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7203345	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7205034	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8059500	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8060276	0.90[AMR][1000 genomes]
rs9788838	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9921760	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9928574	0.86[EUR][1000 genomes]
rs9928704	0.86[AMR][1000 genomes];0.89[EUR][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	nsv905747	chr16:31394179-31888684	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
2	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	esv3446880	chr16:31734687-31891223	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31862000-31866400	Weak transcription	Gastric	stomach

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