Variant report

Variant	rs7649870
Chromosome Location	chr3:18079003-18079004
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs4688914	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4908954	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4908955	0.87[ASN][1000 genomes]
rs4909001	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4909005	0.84[AMR][1000 genomes]
rs6577608	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6784436	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7428364	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7430739	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7431124	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7432256	0.80[ASN][1000 genomes]
rs7611417	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7627212	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7641293	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7644630	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7646613	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9310539	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9833830	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9878816	0.80[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:18055000-18088000	Weak transcription	Primary hematopoietic stem cells	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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