Variant report

Variant	rs57177321
Chromosome Location	chr11:33988111-33988112
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11032462	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11032463	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11032464	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11032466	0.92[EUR][1000 genomes]
rs11602178	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11603626	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11605421	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11607752	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12417148	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12417766	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12421417	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1518919	0.98[ASN][1000 genomes]
rs16924994	0.94[ASN][1000 genomes]
rs2421466	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35661841	0.87[EUR][1000 genomes]
rs7940933	0.98[ASN][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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