Variant report

Variant	rs9406701
Chromosome Location	chr9:17766416-17766417
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs13300747	0.83[ASN][1000 genomes]
rs13301348	0.88[ASN][1000 genomes]
rs17454653	0.98[ASN][1000 genomes]
rs35004355	0.90[ASN][1000 genomes]
rs35572607	0.98[ASN][1000 genomes]
rs36048313	1.00[ASN][1000 genomes]
rs3808668	0.98[ASN][1000 genomes]
rs3808669	0.98[ASN][1000 genomes]
rs3808672	0.98[ASN][1000 genomes]
rs3808676	0.93[ASN][1000 genomes]
rs3808678	0.90[ASN][1000 genomes]
rs3824371	0.90[ASN][1000 genomes]
rs56371897	0.98[ASN][1000 genomes]
rs56374530	0.90[ASN][1000 genomes]
rs58624127	0.98[ASN][1000 genomes]
rs59114776	0.98[ASN][1000 genomes]
rs60376810	0.98[ASN][1000 genomes]
rs62550981	0.98[ASN][1000 genomes]
rs66488451	0.93[ASN][1000 genomes]
rs7027981	0.81[ASN][1000 genomes]
rs9406697	0.95[ASN][1000 genomes]
rs9406699	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9406700	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9406702	0.98[ASN][1000 genomes]
rs9406703	0.98[ASN][1000 genomes]
rs9406704	0.95[ASN][1000 genomes]
rs9406706	0.95[ASN][1000 genomes]
rs9406707	0.98[ASN][1000 genomes]
rs9406708	0.98[ASN][1000 genomes]
rs9406709	0.98[ASN][1000 genomes]
rs9406710	0.98[ASN][1000 genomes]
rs9406712	0.98[ASN][1000 genomes]
rs9406713	0.98[ASN][1000 genomes]
rs9406714	0.98[ASN][1000 genomes]
rs9406715	0.98[ASN][1000 genomes]
rs9406716	0.98[ASN][1000 genomes]
rs9406717	0.98[ASN][1000 genomes]
rs9406718	0.98[ASN][1000 genomes]
rs9406719	0.98[ASN][1000 genomes]
rs9406720	0.98[ASN][1000 genomes]
rs9406721	0.98[ASN][1000 genomes]
rs9406722	0.98[ASN][1000 genomes]
rs9406723	0.98[ASN][1000 genomes]
rs9406724	0.98[ASN][1000 genomes]
rs9406725	0.98[ASN][1000 genomes]
rs9406726	0.98[ASN][1000 genomes]
rs9406727	0.98[ASN][1000 genomes]
rs9407837	0.84[ASN][1000 genomes]
rs9407838	0.95[ASN][1000 genomes]
rs9407839	0.98[ASN][1000 genomes]
rs9407849	0.98[ASN][1000 genomes]
rs9407850	0.98[ASN][1000 genomes]
rs9407851	0.98[ASN][1000 genomes]
rs9407852	0.98[ASN][1000 genomes]
rs9407853	0.98[ASN][1000 genomes]
rs9407854	0.93[ASN][1000 genomes]
rs9407855	0.98[ASN][1000 genomes]
rs9407856	0.98[ASN][1000 genomes]
rs9407857	0.98[ASN][1000 genomes]
rs9407858	0.98[ASN][1000 genomes]
rs9407859	0.98[ASN][1000 genomes]
rs9407860	0.98[ASN][1000 genomes]
rs9407861	0.98[ASN][1000 genomes]
rs9407862	0.98[ASN][1000 genomes]
rs9407863	0.98[ASN][1000 genomes]
rs9407864	0.98[ASN][1000 genomes]
rs9407865	0.98[ASN][1000 genomes]
rs9407866	0.98[ASN][1000 genomes]
rs9407867	0.98[ASN][1000 genomes]
rs9407868	0.98[ASN][1000 genomes]
rs9407869	0.98[ASN][1000 genomes]
rs9407870	0.95[ASN][1000 genomes]
rs9407871	0.98[ASN][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	nsv892675	chr9:17694823-17790526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv613706	chr9:17718918-18090934	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv613707	chr9:17720175-18070475	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv613708	chr9:17720175-18072085	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1034673	chr9:17739006-17916606	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1023089	chr9:17748811-17919574	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17754800-17772600	Weak transcription	Hela-S3	cervix
2	chr9:17764600-17782800	Weak transcription	Gastric	stomach

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