Variant report

Variant	rs73771859
Chromosome Location	chr5:91708428-91708429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2289344	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6867693	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73771853	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73773838	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73773843	0.81[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91707000-91709200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr5:91707800-91714000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:91708400-91714000	Weak transcription	A549	lung

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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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