Variant report

Variant	rs7992260
Chromosome Location	chr13:92846724-92846725
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12583936	0.86[CEU][hapmap];0.86[EUR][1000 genomes]
rs12876819	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs17233753	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs1998890	0.94[CHB][hapmap]
rs4238302	1.00[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4597182	0.91[CEU][hapmap]
rs4773676	1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61967886	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7326993	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs7990793	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7998228	0.94[CHB][hapmap]
rs874795	0.94[CHB][hapmap]
rs9516020	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs9556159	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs9560962	0.91[CEU][hapmap]
rs9560963	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs9560967	0.91[CEU][hapmap];0.82[CHB][hapmap]
rs9560979	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[EUR][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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv456066	chr13:92694581-92884370	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv562723	chr13:92694581-92884370	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1035365	chr13:92805325-92926114	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1053468	chr13:92814581-92893231	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr13:92846400-92847000	Enhancers	Pancreatic Islets	Pancreatic Islet

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Input of quick search could be:

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

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