Variant report

Variant	rs12319228
Chromosome Location	chr12:45502710-45502711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11182828	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11182839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12299138	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12303847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12304662	1.00[AFR][1000 genomes]
rs12314515	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12317891	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1558987	1.00[AFR][1000 genomes];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	esv3351644	chr12:45345597-45529449	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45502600-45503800	Weak transcription	H1 Derived Neuronal Progenitor 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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