Variant report

Variant	rs73315613
Chromosome Location	chr8:118072114-118072115
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11988506	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11991494	1.00[ASN][1000 genomes]
rs11992440	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1505521	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16889367	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16889399	1.00[ASN][1000 genomes]
rs1857810	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1995580	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59791265	1.00[ASN][1000 genomes]
rs60124396	1.00[ASN][1000 genomes]
rs60337074	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6469674	1.00[ASN][1000 genomes]
rs6469678	1.00[ASN][1000 genomes]
rs6996470	1.00[ASN][1000 genomes]
rs7001168	1.00[ASN][1000 genomes]
rs7004777	1.00[ASN][1000 genomes]
rs73315618	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73315629	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73315653	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73315659	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73315665	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73315666	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73315671	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73315672	0.88[AMR][1000 genomes]
rs73317621	1.00[ASN][1000 genomes]
rs73317630	1.00[ASN][1000 genomes]
rs73317635	1.00[ASN][1000 genomes]
rs73317638	1.00[ASN][1000 genomes]
rs73317641	1.00[ASN][1000 genomes]
rs7464559	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7827851	1.00[ASN][1000 genomes]
rs7832958	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1027920	chr8:117983619-118079816	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv539732	chr8:117983619-118079816	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118058200-118073800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr8:118068400-118073200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:118069400-118074000	Weak transcription	HSMMtube	muscle
4	chr8:118070800-118076000	Enhancers	Fetal Stomach	stomach
5	chr8:118070800-118076800	Enhancers	Fetal Lung	lung
6	chr8:118071800-118077000	Enhancers	Fetal Muscle Leg	muscle

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