Variant report

Variant	rs7335555
Chromosome Location	chr13:92860862-92860863
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10492504	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1172297	0.83[CEU][hapmap]
rs1177726	1.00[CEU][hapmap]
rs11842003	1.00[JPT][hapmap]
rs1330978	0.94[CEU][hapmap]
rs1330995	1.00[CEU][hapmap]
rs1360390	1.00[JPT][hapmap]
rs1360391	1.00[JPT][hapmap]
rs1360392	1.00[JPT][hapmap]
rs1360393	1.00[JPT][hapmap]
rs1411751	1.00[CEU][hapmap]
rs16947132	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs16947150	1.00[CEU][hapmap]
rs17426071	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1819439	1.00[CEU][hapmap]
rs1888545	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1998890	0.82[YRI][hapmap]
rs2148521	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2148523	1.00[JPT][hapmap]
rs2182533	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2209651	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3803208	1.00[JPT][hapmap]
rs4281579	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4408406	1.00[CEU][hapmap]
rs4559792	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4771854	0.94[CEU][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57786284	0.93[EUR][1000 genomes]
rs59410447	0.90[EUR][1000 genomes]
rs6492591	0.82[YRI][hapmap]
rs6650316	1.00[CEU][hapmap]
rs72636830	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72636832	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72636834	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72636840	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7333645	1.00[JPT][hapmap]
rs7334533	1.00[CEU][hapmap]
rs7336644	0.94[CEU][hapmap]
rs7489550	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7981670	1.00[JPT][hapmap]
rs7987741	0.94[CEU][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7991537	1.00[JPT][hapmap]
rs7998228	0.94[YRI][hapmap]
rs874795	0.88[YRI][hapmap]
rs880546	0.94[CEU][hapmap]
rs9301783	1.00[JPT][hapmap]
rs9516020	0.82[YRI][hapmap]
rs9523535	0.94[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9556163	1.00[CEU][hapmap]
rs9560960	1.00[JPT][hapmap]
rs9560961	1.00[JPT][hapmap]
rs9560972	1.00[JPT][hapmap]
rs9560973	1.00[JPT][hapmap]
rs9560974	1.00[JPT][hapmap]
rs9560977	1.00[JPT][hapmap]
rs9560981	1.00[JPT][hapmap]
rs9560982	0.93[CEU][hapmap];1.00[JPT][hapmap]
rs9560983	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9560984	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs9560985	0.93[EUR][1000 genomes]
rs9560986	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs9560988	1.00[CEU][hapmap]
rs9560995	1.00[JPT][hapmap]
rs9560997	1.00[JPT][hapmap]
rs9583999	1.00[JPT][hapmap]
rs9589454	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[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	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:0 , 50 per page) page:

No data

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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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