Variant report

Variant	rs9589831
Chromosome Location	chr13:94440487-94440488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12323273	1.00[AMR][1000 genomes]
rs2150126	1.00[AMR][1000 genomes]
rs28460048	1.00[AMR][1000 genomes]
rs9584156	1.00[AMR][1000 genomes]
rs9584158	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9584159	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9584160	1.00[AMR][1000 genomes]
rs9584162	1.00[AMR][1000 genomes]
rs9584168	1.00[AMR][1000 genomes]
rs9589828	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589829	1.00[AMR][1000 genomes]
rs9589830	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589835	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589838	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589840	1.00[AMR][1000 genomes]
rs9589843	1.00[AMR][1000 genomes]
rs9589844	1.00[AMR][1000 genomes]
rs9589845	1.00[AMR][1000 genomes]
rs9589846	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589847	1.00[AMR][1000 genomes]
rs9589849	1.00[AMR][1000 genomes]
rs9589850	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9589855	1.00[AMR][1000 genomes]
rs9589856	1.00[AMR][1000 genomes]
rs9589864	1.00[AMR][1000 genomes]
rs9589865	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1045230	chr13:94277683-94764671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv832684	chr13:94379507-94550853	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1130	chr13:94410849-94455628	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94439600-94448800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:94439800-94440800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr13:94440400-94441400	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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