Variant report

Variant	rs73953210
Chromosome Location	chr2:125631435-125631436
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]
rs1482838	0.86[ASN][1000 genomes]
rs17012034	0.81[ASN][1000 genomes]
rs17012037	0.81[ASN][1000 genomes]
rs17012041	0.90[ASN][1000 genomes]
rs17012116	0.95[ASN][1000 genomes]
rs55906816	0.90[ASN][1000 genomes]
rs57373389	0.95[ASN][1000 genomes]
rs58960665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs59648005	0.90[ASN][1000 genomes]
rs60413051	1.00[ASN][1000 genomes]
rs6716689	0.90[ASN][1000 genomes]
rs73955847	0.81[ASN][1000 genomes]
rs73955850	0.90[ASN][1000 genomes]
rs73955853	0.90[ASN][1000 genomes]
rs7605407	0.81[ASN][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	nsv834360	chr2:125492685-125683200	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv834361	chr2:125601081-125810992	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 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	chr2:125629200-125637000	Weak transcription	Gastric	stomach
2	chr2:125631400-125632400	Weak transcription	Stomach Mucosa	stomach

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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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