Variant report

Variant	rs1607263
Chromosome Location	chr2:180360291-180360292
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10197005	0.80[ASN][1000 genomes]
rs10930875	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11686958	0.92[ASN][1000 genomes]
rs11693292	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12989888	0.89[EUR][1000 genomes]
rs12990747	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13007260	0.88[EUR][1000 genomes]
rs1400820	0.80[ASN][1000 genomes]
rs1607264	0.92[ASN][1000 genomes]
rs16866747	0.90[EUR][1000 genomes]
rs34822738	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34880595	0.88[EUR][1000 genomes]
rs35959339	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4894102	0.88[EUR][1000 genomes]
rs4894104	0.80[ASN][1000 genomes]
rs58313907	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72950544	0.89[EUR][1000 genomes]
rs72950575	0.86[ASN][1000 genomes]
rs7589355	0.87[EUR][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	nsv875468	chr2:180352334-180396869	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv875469	chr2:180354642-180396869	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180350600-180367200	Weak transcription	Liver	Liver
2	chr2:180352600-180360600	Weak transcription	Fetal Intestine Large	intestine
3	chr2:180352800-180378400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:180358400-180367800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:180360200-180360400	Enhancers	Gastric	stomach

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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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