Variant report

Variant	rs10961187
Chromosome Location	chr9:13657571-13657572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10435725	0.87[ASN][1000 genomes]
rs10810002	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10961191	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10961195	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11998882	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12237961	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17193343	0.92[ASN][1000 genomes]
rs17193379	0.92[ASN][1000 genomes]
rs55688876	0.83[ASN][1000 genomes]
rs55992305	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6474790	0.83[ASN][1000 genomes]
rs6474791	0.81[ASN][1000 genomes]
rs7025981	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7041117	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7041906	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7045171	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7847902	0.92[ASN][1000 genomes]
rs7849359	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7850099	0.82[ASN][1000 genomes]
rs7852661	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7855395	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7872836	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7873377	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7873424	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7876011	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8192964	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs8192971	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs8192977	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs942389	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023684	chr9:13529680-13744602	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv540067	chr9:13529680-13744602	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892587	chr9:13601074-13732363	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1843958	chr9:13631992-13706651	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	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	chr9:13651600-13660800	Weak transcription	Right Atrium	heart

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