Variant report

Variant	rs13233758
Chromosome Location	chr7:13560618-13560619
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10499429	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12699504	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12699509	1.00[ASN][1000 genomes]
rs12699514	1.00[ASN][1000 genomes]
rs12699515	1.00[ASN][1000 genomes]
rs12699521	1.00[ASN][1000 genomes]
rs12699522	1.00[ASN][1000 genomes]
rs12699523	1.00[ASN][1000 genomes]
rs12699526	1.00[ASN][1000 genomes]
rs12699527	1.00[ASN][1000 genomes]
rs12699533	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13222945	1.00[ASN][1000 genomes]
rs13223388	1.00[ASN][1000 genomes]
rs13223397	1.00[ASN][1000 genomes]
rs13226153	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13226865	1.00[ASN][1000 genomes]
rs13229998	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13230082	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13234130	1.00[ASN][1000 genomes]
rs13234879	1.00[ASN][1000 genomes]
rs13235921	1.00[ASN][1000 genomes]
rs13237232	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13238361	1.00[ASN][1000 genomes]
rs13243211	1.00[ASN][1000 genomes]
rs1357978	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1357979	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525678	1.00[ASN][1000 genomes]
rs17194917	1.00[ASN][1000 genomes]
rs34575271	1.00[ASN][1000 genomes]
rs34817842	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35137805	1.00[ASN][1000 genomes]
rs35519947	1.00[ASN][1000 genomes]
rs35553190	1.00[ASN][1000 genomes]
rs35657075	1.00[ASN][1000 genomes]
rs35907373	1.00[ASN][1000 genomes]
rs35907984	1.00[ASN][1000 genomes]
rs36068685	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4721234	1.00[ASN][1000 genomes]
rs4721237	1.00[ASN][1000 genomes]
rs67184261	1.00[ASN][1000 genomes]
rs6951342	1.00[ASN][1000 genomes]
rs6955662	1.00[ASN][1000 genomes]
rs6961459	1.00[ASN][1000 genomes]
rs6978901	1.00[ASN][1000 genomes]
rs6979071	1.00[ASN][1000 genomes]
rs7778160	1.00[ASN][1000 genomes]
rs7789334	1.00[ASN][1000 genomes]
rs869552	1.00[AFR][1000 genomes];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	nsv1019173	chr7:13063854-13585360	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538737	chr7:13063854-13585360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1023580	chr7:13403531-13624975	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr7:13559000-13562200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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