Variant report

Variant	rs72683761
Chromosome Location	chr14:78658689-78658690
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs100611	0.84[AFR][1000 genomes]
rs12895757	0.86[ASN][1000 genomes]
rs213562	0.83[AMR][1000 genomes]
rs213565	0.94[AFR][1000 genomes]
rs213566	0.94[ASN][1000 genomes]
rs4903720	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4903724	0.94[ASN][1000 genomes]
rs55935389	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8010446	0.96[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	nsv1366	chr14:78633044-78677718	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78648000-78659000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:78652600-78660200	Weak transcription	Brain Germinal Matrix	brain

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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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