Variant report

Variant	rs74080382
Chromosome Location	chr13:51583980-51583981
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17075139	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2281993	0.97[ASN][1000 genomes]
rs2296914	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3790031	0.92[EUR][1000 genomes]
rs58094875	0.89[ASN][1000 genomes]
rs60194361	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7317089	0.87[ASN][1000 genomes]
rs7333942	0.87[ASN][1000 genomes]
rs7339210	0.87[ASN][1000 genomes]
rs74080386	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74080387	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74080392	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs74080393	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74080395	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51581200-51588000	Weak transcription	Aorta	Aorta
2	chr13:51583000-51584200	Enhancers	Fetal Intestine Large	intestine
3	chr13:51583800-51584200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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