Variant report

Variant	rs7991537
Chromosome Location	chr13:92828380-92828381
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10492504	1.00[CHB][hapmap]
rs1172297	1.00[CHB][hapmap]
rs1177726	1.00[CHB][hapmap]
rs11842003	1.00[JPT][hapmap]
rs1330978	1.00[CHB][hapmap]
rs1330982	1.00[CHB][hapmap]
rs1330983	1.00[CHB][hapmap]
rs1330984	1.00[CHB][hapmap]
rs1330995	1.00[CHB][hapmap]
rs1360390	1.00[JPT][hapmap]
rs1360391	1.00[JPT][hapmap]
rs1360392	1.00[JPT][hapmap]
rs1360393	1.00[JPT][hapmap]
rs1411747	1.00[CHB][hapmap]
rs16947132	1.00[CHB][hapmap]
rs16947150	1.00[CHB][hapmap]
rs17267151	1.00[CHB][hapmap]
rs17299487	1.00[CEU][hapmap]
rs17299494	1.00[CEU][hapmap]
rs17426071	1.00[CHB][hapmap]
rs2148521	1.00[CHB][hapmap]
rs2148523	1.00[JPT][hapmap]
rs2182533	1.00[CHB][hapmap]
rs2209651	1.00[CHB][hapmap]
rs3803208	1.00[JPT][hapmap]
rs4408406	1.00[CHB][hapmap]
rs4771854	1.00[CHB][hapmap]
rs6650316	1.00[CHB][hapmap]
rs7333645	1.00[JPT][hapmap]
rs7334533	1.00[CHB][hapmap]
rs7335555	1.00[JPT][hapmap]
rs7336644	1.00[CHB][hapmap]
rs7489550	1.00[CHB][hapmap]
rs7981670	1.00[JPT][hapmap]
rs7987741	1.00[CHB][hapmap]
rs880546	1.00[CHB][hapmap]
rs9301781	1.00[CHB][hapmap]
rs9301782	1.00[CHB][hapmap]
rs9301783	1.00[JPT][hapmap]
rs9523526	1.00[CHB][hapmap]
rs9523535	1.00[CHB][hapmap]
rs9556163	1.00[CHB][hapmap]
rs9560938	1.00[CEU][hapmap]
rs9560939	1.00[CEU][hapmap]
rs9560940	1.00[CEU][hapmap]
rs9560942	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	1.00[CHB][hapmap]
rs9560983	1.00[CHB][hapmap]
rs9560984	1.00[CHB][hapmap]
rs9560986	1.00[CHB][hapmap]
rs9560988	1.00[CHB][hapmap]
rs9560995	1.00[JPT][hapmap]
rs9560997	1.00[JPT][hapmap]
rs9583999	1.00[JPT][hapmap]

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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