Variant report

Variant	rs1518920
Chromosome Location	chr11:33988311-33988312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10444269	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10444270	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10768037	0.84[EUR][1000 genomes]
rs10768038	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10836135	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12273291	0.85[EUR][1000 genomes]
rs2421467	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs4996144	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6484685	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6484686	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7104709	0.81[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33983200-33992400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:33985600-33991000	Weak transcription	K562	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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