Variant report

Variant	rs2260497
Chromosome Location	chr1:71256507-71256508
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10493479	1.00[ASN][1000 genomes]
rs10889887	0.98[ASN][1000 genomes]
rs11209689	0.98[ASN][1000 genomes]
rs11209696	0.99[ASN][1000 genomes]
rs12080803	1.00[ASN][1000 genomes]
rs12141856	0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs1327458	1.00[ASN][1000 genomes]
rs1536536	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2148800	1.00[ASN][1000 genomes]
rs2257772	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2258875	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7523175	1.00[ASN][1000 genomes]
rs7547597	1.00[ASN][1000 genomes]
rs7555485	0.98[ASN][1000 genomes]
rs7555865	0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71256400-71256800	Enhancers	Primary T cells from cord blood	blood

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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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