Variant report

Variant	rs983387
Chromosome Location	chr4:81250516-81250517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10016626	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11099145	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs11099173	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11099174	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12503208	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13110939	0.96[ASN][1000 genomes]
rs13141004	0.84[AFR][1000 genomes]
rs1458032	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs1458033	0.96[ASN][1000 genomes]
rs1458034	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1841011	0.91[ASN][1000 genomes]
rs1841012	0.92[ASN][1000 genomes]
rs2867709	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs3899052	0.96[ASN][1000 genomes]
rs4690118	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4690152	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6811219	0.98[ASN][1000 genomes]
rs6822305	0.84[CEU][hapmap];0.97[ASN][1000 genomes]
rs728956	0.92[ASN][1000 genomes]
rs747125	0.92[ASN][1000 genomes]
rs7667119	0.84[AMR][1000 genomes]
rs7678815	0.98[ASN][1000 genomes]
rs7688097	0.96[ASN][1000 genomes]
rs7698854	0.97[ASN][1000 genomes]
rs968376	0.96[ASN][1000 genomes]
rs983388	0.98[ASN][1000 genomes]
rs9993841	0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81249200-81250600	Weak transcription	Fetal Heart	heart

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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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