Variant report

Variant	rs9986786
Chromosome Location	chr7:39237586-39237587
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	chr7:39229548..39232422-chr7:39234869..39240072,4	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10224345	1.00[ASN][1000 genomes]
rs10234489	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10235824	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10248402	1.00[ASN][1000 genomes]
rs10254999	1.00[ASN][1000 genomes]
rs10269214	1.00[ASN][1000 genomes]
rs10277485	1.00[ASN][1000 genomes]
rs1229057	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1405987	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs1525790	1.00[ASN][1000 genomes]
rs1527953	1.00[ASN][1000 genomes]
rs1527957	1.00[ASN][1000 genomes]
rs1534415	1.00[ASN][1000 genomes]
rs1881131	1.00[ASN][1000 genomes]
rs1950001	1.00[ASN][1000 genomes]
rs2140910	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs2893570	1.00[ASN][1000 genomes]
rs4294102	1.00[ASN][1000 genomes]
rs4452709	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4499996	1.00[ASN][1000 genomes]
rs4499997	1.00[ASN][1000 genomes]
rs4507668	1.00[ASN][1000 genomes]
rs4588755	1.00[ASN][1000 genomes]
rs4723826	1.00[ASN][1000 genomes]
rs4723830	1.00[ASN][1000 genomes]
rs6955794	1.00[ASN][1000 genomes]
rs6971923	1.00[ASN][1000 genomes]
rs702820	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs73121830	1.00[ASN][1000 genomes]
rs73122445	1.00[ASN][1000 genomes]
rs73126431	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73126469	1.00[ASN][1000 genomes]
rs73127520	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73127523	1.00[ASN][1000 genomes]
rs7778249	1.00[ASN][1000 genomes]
rs7778299	1.00[ASN][1000 genomes]
rs7787883	1.00[ASN][1000 genomes]
rs859513	1.00[ASN][1000 genomes]
rs859542	1.00[ASN][1000 genomes]
rs859545	0.84[CEU][hapmap];1.00[ASN][1000 genomes]
rs859546	1.00[ASN][1000 genomes]
rs9987012	1.00[ASN][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	nsv1024142	chr7:38978728-39300444	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830968	chr7:39127531-39283543	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv428163	chr7:39127531-39283543	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1015572	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv538821	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39215000-39247000	Weak transcription	Pancreas	Pancrea
2	chr7:39232000-39252400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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