Variant report

Variant	rs35734631
Chromosome Location	chr7:103536151-103536152
allele	A/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]
rs10226733	0.84[ASN][1000 genomes]
rs10270408	0.84[ASN][1000 genomes]
rs12667097	1.00[ASN][1000 genomes]
rs17157005	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17157010	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17157043	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17157057	0.91[ASN][1000 genomes]
rs17157072	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17157084	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17157104	1.00[ASN][1000 genomes]
rs17157114	1.00[AMR][1000 genomes];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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103531000-103536600	Weak transcription	K562	blood
2	chr7:103531200-103546000	Weak transcription	HepG2	liver
3	chr7:103535000-103536200	Enhancers	Brain Germinal Matrix	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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