Variant report

Variant	rs987382
Chromosome Location	chr4:96547093-96547094
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13103169	0.88[ASN][1000 genomes]
rs13128524	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13129583	0.82[EUR][1000 genomes]
rs13130278	0.81[EUR][1000 genomes]
rs1369985	0.90[ASN][1000 genomes]
rs17024349	0.81[CEU][hapmap]
rs1946735	0.82[ASN][1000 genomes]
rs2043657	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35403357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6841996	0.87[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96544000-96549000	Weak transcription	Aorta	Aorta
2	chr4:96546600-96547200	Enhancers	Fetal Stomach	stomach

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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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