Variant report

Variant	rs7537290
Chromosome Location	chr1:165594900-165594901
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10918220	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10918226	1.00[ASN][1000 genomes]
rs1538114	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147147	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4147148	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6657788	0.97[AMR][1000 genomes]
rs6658200	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6672933	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6677016	0.87[EUR][1000 genomes]
rs6679939	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9333468	1.00[ASN][1000 genomes]
rs9333476	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165594000-165599000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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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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