Variant report

Variant	rs61458713
Chromosome Location	chr19:45065230-45065231
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12977854	1.00[ASN][1000 genomes]
rs35401363	1.00[ASN][1000 genomes]
rs4803741	1.00[ASN][1000 genomes]
rs62119329	1.00[ASN][1000 genomes]
rs62120564	1.00[ASN][1000 genomes]
rs73046432	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73561940	1.00[ASN][1000 genomes]
rs73561943	1.00[ASN][1000 genomes]
rs73561968	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74172479	1.00[ASN][1000 genomes]
rs8107008	1.00[ASN][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	nsv1062812	chr19:45042262-45214796	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 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	chr19:45065200-45070200	Weak transcription	HepG2	liver

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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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