Variant report

Variant	rs72675652
Chromosome Location	chr8:91350830-91350831
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:16)

rs_ID	r²[population]
rs10086788	0.86[ASN][1000 genomes]
rs10099647	0.86[ASN][1000 genomes]
rs10103125	0.86[ASN][1000 genomes]
rs10104451	0.86[ASN][1000 genomes]
rs10111531	0.86[ASN][1000 genomes]
rs10112676	0.86[ASN][1000 genomes]
rs16904523	0.86[ASN][1000 genomes]
rs1859178	1.00[AFR][1000 genomes]
rs28385552	0.86[ASN][1000 genomes]
rs28687302	0.86[ASN][1000 genomes]
rs28715738	0.86[ASN][1000 genomes]
rs4474067	0.86[ASN][1000 genomes]
rs58836045	0.86[ASN][1000 genomes]
rs6470923	1.00[AFR][1000 genomes]
rs72675661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7817151	1.00[AFR][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	nsv1018991	chr8:91336887-91374274	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr8:91337000-91353200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:91350600-91352000	Strong transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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