Variant report

Variant	rs1718082
Chromosome Location	chr7:146095538-146095539
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10226676	0.92[EUR][1000 genomes]
rs10227977	1.00[ASN][1000 genomes]
rs10231549	1.00[ASN][1000 genomes]
rs10231672	1.00[ASN][1000 genomes]
rs10242387	0.92[EUR][1000 genomes]
rs10256837	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10258224	1.00[ASN][1000 genomes]
rs10273261	1.00[ASN][1000 genomes]
rs10275558	1.00[ASN][1000 genomes]
rs10280011	1.00[ASN][1000 genomes]
rs10487935	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1358079	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1358082	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1358083	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403008	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403009	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403010	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1526162	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1639478	1.00[ASN][1000 genomes]
rs1639479	1.00[ASN][1000 genomes]
rs1639485	1.00[ASN][1000 genomes]
rs1639487	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1639489	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1718073	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1718074	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1718075	1.00[ASN][1000 genomes]
rs1718077	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1718078	1.00[ASN][1000 genomes]
rs1718080	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1718081	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1724526	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724527	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724529	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724531	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724535	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724536	1.00[ASN][1000 genomes]
rs2535752	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28687551	1.00[ASN][1000 genomes]
rs60409856	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73738703	1.00[ASN][1000 genomes]
rs73738715	1.00[ASN][1000 genomes]
rs73738756	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889384	chr7:145541783-146239545	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1020950	chr7:145683419-146264304	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv889387	chr7:145903862-146239545	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv533345	chr7:145934546-146134958	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv889389	chr7:145998111-146121539	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv917027	chr7:146069317-146194011	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1024679	chr7:146091479-146248268	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr7:146089000-146109400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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