Variant report

Variant	rs35596772
Chromosome Location	chr9:71248578-71248579
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10511959	1.00[ASN][1000 genomes]
rs13284137	1.00[ASN][1000 genomes]
rs13288798	1.00[ASN][1000 genomes]
rs13288885	1.00[ASN][1000 genomes]
rs13290124	1.00[ASN][1000 genomes]
rs13296119	1.00[ASN][1000 genomes]
rs13297946	1.00[ASN][1000 genomes]
rs17479202	1.00[ASN][1000 genomes]
rs34054758	1.00[ASN][1000 genomes]
rs34206324	1.00[ASN][1000 genomes]
rs34267520	1.00[ASN][1000 genomes]
rs34344868	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34377966	1.00[ASN][1000 genomes]
rs34412731	1.00[ASN][1000 genomes]
rs34436601	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34532945	1.00[ASN][1000 genomes]
rs34763246	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35029924	1.00[ASN][1000 genomes]
rs35551873	1.00[ASN][1000 genomes]
rs35666199	1.00[ASN][1000 genomes]
rs6560237	1.00[ASN][1000 genomes]
rs7045561	1.00[ASN][1000 genomes]
rs7048633	1.00[ASN][1000 genomes]
rs71501771	1.00[ASN][1000 genomes]
rs71503634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs772	1.00[ASN][1000 genomes]
rs7858883	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7859065	1.00[ASN][1000 genomes]
rs7863262	0.91[AMR][1000 genomes];0.91[EUR][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	nsv482506	chr9:71130848-71280888	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv466392	chr9:71130848-71318817	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv614546	chr9:71130848-71318817	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv893414	chr9:71139378-71320732	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	esv2422258	chr9:71234845-71663340	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 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	chr9:71247400-71249000	Weak transcription	Fetal Heart	heart

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