Variant report

Variant	rs10088589
Chromosome Location	chr8:34426231-34426232
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10089235	1.00[AFR][1000 genomes]
rs10107705	0.81[AFR][1000 genomes]
rs28557310	0.91[AFR][1000 genomes]
rs28584195	0.82[AFR][1000 genomes]
rs28614027	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2153880	chr8:34426007-34426442	Enhancers	n/a	n/a	inside rSNPs	diseases
2	esv3431993	chr8:34426065-34426338	Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv3503904	chr8:34426099-34426317	Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3424360	chr8:34426130-34426302	Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv3424052	chr8:34426150-34426272	Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3481154	chr8:34426175-34426257	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3503905	chr8:34426185-34426255	Enhancers	n/a	n/a	inside rSNPs	diseases
8	nsv396306	chr8:34426189-34426252	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3481155	chr8:34426189-34426253	Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3503906	chr8:34426189-34426253	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34426200-34426800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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