Variant report

Variant	rs10151264
Chromosome Location	chr14:63357696-63357697
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10134277	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10143260	0.94[ASN][1000 genomes]
rs10143966	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10483759	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10483762	0.85[ASN][1000 genomes]
rs12587225	0.84[ASN][1000 genomes]
rs12587258	0.84[ASN][1000 genomes]
rs12881527	0.91[ASN][1000 genomes]
rs17223580	0.94[ASN][1000 genomes]
rs17823609	0.94[ASN][1000 genomes]
rs2144775	0.96[ASN][1000 genomes]
rs4899100	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57087381	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59454582	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs8015097	0.99[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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63356800-63362400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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

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