Variant report

Variant	rs58783663
Chromosome Location	chr8:119330594-119330595
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10102091	0.93[ASN][1000 genomes]
rs10102185	0.93[ASN][1000 genomes]
rs10102483	0.93[ASN][1000 genomes]
rs10481135	0.84[EUR][1000 genomes]
rs10955871	0.91[ASN][1000 genomes]
rs11782250	0.91[ASN][1000 genomes]
rs11994015	0.80[EUR][1000 genomes]
rs12155712	0.83[EUR][1000 genomes]
rs12156385	0.89[ASN][1000 genomes]
rs13248150	0.82[EUR][1000 genomes]
rs1385806	0.93[ASN][1000 genomes]
rs1385807	0.93[ASN][1000 genomes]
rs1545925	0.90[ASN][1000 genomes]
rs1843535	0.90[ASN][1000 genomes]
rs1905938	0.80[ASN][1000 genomes]
rs28493856	0.91[ASN][1000 genomes]
rs28558308	0.90[ASN][1000 genomes]
rs34008405	0.84[ASN][1000 genomes]
rs34458847	0.93[ASN][1000 genomes]
rs34727859	0.93[ASN][1000 genomes]
rs35027398	0.93[ASN][1000 genomes]
rs35246465	0.93[ASN][1000 genomes]
rs35595491	0.93[ASN][1000 genomes]
rs35812722	0.88[ASN][1000 genomes]
rs3802185	0.91[ASN][1000 genomes]
rs4496996	0.92[ASN][1000 genomes]
rs4571758	0.93[ASN][1000 genomes]
rs4592080	0.93[ASN][1000 genomes]
rs4628280	0.90[ASN][1000 genomes]
rs4876409	0.90[ASN][1000 genomes]
rs6469731	0.92[ASN][1000 genomes]
rs6469732	0.92[ASN][1000 genomes]
rs6469733	0.92[ASN][1000 genomes]
rs6469734	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6980537	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6980779	0.81[ASN][1000 genomes]
rs6987634	0.93[ASN][1000 genomes]
rs6991597	0.92[ASN][1000 genomes]
rs6994128	0.82[EUR][1000 genomes]
rs6994270	0.82[EUR][1000 genomes]
rs6996584	0.91[ASN][1000 genomes]
rs6996602	0.93[EUR][1000 genomes]
rs7008611	0.82[EUR][1000 genomes]
rs7009206	0.92[ASN][1000 genomes]
rs7010323	0.83[ASN][1000 genomes]
rs7018387	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs71515964	0.93[ASN][1000 genomes]
rs73323697	0.80[EUR][1000 genomes]
rs7817627	0.93[ASN][1000 genomes]
rs7819713	0.82[ASN][1000 genomes]
rs7820290	0.80[ASN][1000 genomes]
rs7820498	0.84[ASN][1000 genomes]
rs7823536	0.90[ASN][1000 genomes]
rs7823689	0.90[ASN][1000 genomes]
rs7827637	0.82[EUR][1000 genomes]
rs7828165	0.90[ASN][1000 genomes]
rs7828224	0.92[ASN][1000 genomes]
rs7828542	0.92[ASN][1000 genomes]
rs7831174	0.93[EUR][1000 genomes]
rs7831226	0.91[ASN][1000 genomes]
rs7832024	0.84[EUR][1000 genomes]
rs7836216	0.87[ASN][1000 genomes]
rs7837752	0.82[ASN][1000 genomes]
rs7838723	0.84[ASN][1000 genomes]
rs7841049	0.92[ASN][1000 genomes]
rs7841856	0.90[ASN][1000 genomes]
rs9642839	0.93[ASN][1000 genomes]
rs9694445	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv1015380	chr8:118948652-119418389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv539736	chr8:118948652-119418389	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	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
5	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
6	nsv1016379	chr8:119164234-119448910	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv831442	chr8:119181675-119390122	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
8	nsv8382	chr8:119324224-119341066	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1308352	chr8:119330581-119330595	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119323000-119357600	Weak transcription	Aorta	Aorta
2	chr8:119323000-119394000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:119323800-119362400	Weak transcription	GM12878-XiMat	blood
4	chr8:119324400-119338000	Weak transcription	Small Intestine	intestine

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