Variant report

Variant	rs2045704
Chromosome Location	chr11:26419422-26419423
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1023902	1.00[CEU][hapmap];0.81[YRI][hapmap]
rs12289490	0.88[TSI][hapmap]
rs1461372	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs1461375	1.00[CEU][hapmap]
rs1461381	1.00[CEU][hapmap]
rs1841569	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap]
rs2169340	1.00[CEU][hapmap]
rs2201335	0.85[CEU][hapmap]
rs2219616	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs4500442	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs4505017	0.85[CEU][hapmap]
rs7945236	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs986059	1.00[CEU][hapmap];0.83[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	esv2422406	chr11:26329870-26473641	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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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