Variant report

Variant	rs10133680
Chromosome Location	chr14:63295179-63295180
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10047851	0.85[YRI][hapmap]
rs10130817	0.85[YRI][hapmap]
rs10136167	0.85[YRI][hapmap]
rs10139268	0.82[YRI][hapmap]
rs10145825	1.00[YRI][hapmap]
rs10148076	0.85[YRI][hapmap]
rs10483757	0.85[YRI][hapmap]
rs10873163	0.85[YRI][hapmap]
rs1950568	0.85[YRI][hapmap]
rs4899096	0.85[YRI][hapmap]
rs4902191	0.85[YRI][hapmap]
rs9323422	0.85[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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