Variant report

Variant	rs2095752
Chromosome Location	chr1:211398623-211398624
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11581409	0.85[ASN][1000 genomes]
rs12071464	0.99[ASN][1000 genomes]
rs2095753	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3111245	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3111246	0.83[ASN][1000 genomes]
rs3125832	0.81[ASN][1000 genomes]
rs3125833	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57331968	0.88[ASN][1000 genomes]
rs61850977	0.99[ASN][1000 genomes]
rs61850982	0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211395800-211399000	Enhancers	K562	blood
2	chr1:211397800-211405200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr1:211398400-211399200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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