Variant report

Variant	rs17867257
Chromosome Location	chr7:126684300-126684301
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000179562	Chromatin interaction
ENSG00000106328	Chromatin interaction
ENSG00000179603	Chromatin interaction
ENSG00000048405	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10081237	1.00[AMR][1000 genomes]
rs10225020	1.00[YRI][hapmap]
rs10233335	1.00[YRI][hapmap]
rs10239617	1.00[AMR][1000 genomes]
rs10240626	1.00[AMR][1000 genomes]
rs10252488	1.00[AMR][1000 genomes]
rs10254174	1.00[AMR][1000 genomes]
rs10262861	1.00[AMR][1000 genomes]
rs17865523	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17866100	1.00[YRI][hapmap]
rs17866102	1.00[YRI][hapmap]
rs17866773	1.00[YRI][hapmap]
rs17867043	1.00[AMR][1000 genomes]
rs17869242	0.83[YRI][hapmap]
rs17869369	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17869370	1.00[AMR][1000 genomes]

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	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	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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