Variant report

Variant	rs9649313
Chromosome Location	chr7:108503950-108503951
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:108501024..108502651-chr7:108503799..108506089,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10224425	1.00[ASN][1000 genomes]
rs1100226	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1100227	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12705501	1.00[ASN][1000 genomes]
rs12705520	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404686	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404687	1.00[ASN][1000 genomes]
rs1404689	1.00[ASN][1000 genomes]
rs1525181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525198	1.00[ASN][1000 genomes]
rs1525200	1.00[ASN][1000 genomes]
rs1525202	1.00[ASN][1000 genomes]
rs1568856	1.00[ASN][1000 genomes]
rs1568857	1.00[ASN][1000 genomes]
rs1568858	1.00[ASN][1000 genomes]
rs1830037	0.94[ASN][1000 genomes]
rs2396032	0.97[ASN][1000 genomes]
rs2396034	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4730333	0.97[ASN][1000 genomes]
rs4730335	0.87[ASN][1000 genomes]
rs56897220	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58749654	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6466256	0.97[ASN][1000 genomes]
rs6976706	1.00[ASN][1000 genomes]
rs7384561	1.00[ASN][1000 genomes]
rs7781125	1.00[ASN][1000 genomes]
rs7781585	1.00[ASN][1000 genomes]
rs7782139	0.97[ASN][1000 genomes]
rs7786936	1.00[ASN][1000 genomes]
rs848409	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs848410	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs848412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs848413	0.84[AFR][1000 genomes]
rs848415	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][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	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1031096	chr7:108334543-108596014	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv888945	chr7:108445757-108521842	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108503600-108504200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:108503800-108504200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:108503800-108504200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:108503800-108504200	ZNF genes & repeats	Gastric	stomach
5	chr7:108503800-108504200	ZNF genes & repeats	Pancreas	Pancrea

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