Variant report

Variant	rs57102518
Chromosome Location	chr3:118587408-118587409
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1081905	1.00[AMR][1000 genomes]
rs1081906	1.00[EUR][1000 genomes]
rs1081918	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16829026	1.00[EUR][1000 genomes]
rs2099487	1.00[EUR][1000 genomes]
rs2173626	1.00[AMR][1000 genomes]
rs3021393	1.00[AMR][1000 genomes]
rs4687933	1.00[AMR][1000 genomes]
rs6775355	1.00[AMR][1000 genomes]
rs6791688	1.00[AMR][1000 genomes]
rs73854700	1.00[EUR][1000 genomes]
rs798570	1.00[AMR][1000 genomes]
rs798573	1.00[AMR][1000 genomes]
rs9682347	1.00[EUR][1000 genomes]
rs9683131	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118581200-118590000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:118586800-118587800	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr3:118587000-118587600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118587200-118587600	Enhancers	Fetal Brain Female	brain

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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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