Variant report

Variant	rs73290155
Chromosome Location	chr8:90239148-90239149
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10086675	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10093903	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10102110	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10103063	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10104601	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10109917	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10111206	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10955972	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11986218	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11991364	1.00[EUR][1000 genomes]
rs11996831	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12114192	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12114193	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12114437	1.00[EUR][1000 genomes]
rs13438995	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28516901	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28687906	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28810389	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28833856	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs318255	1.00[EUR][1000 genomes]
rs318257	1.00[EUR][1000 genomes]
rs318263	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs318264	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73290158	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73292241	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292247	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292254	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292261	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292264	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292265	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292278	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292279	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73292280	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73294145	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73294147	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73294170	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73295660	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73295669	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73696414	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73696416	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7833277	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1024956	chr8:90104423-90459539	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv539671	chr8:90104423-90459539	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1034759	chr8:90152834-90252502	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv821658	chr8:90199535-90245081	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90238800-90239200	Weak transcription	Fetal Heart	heart

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