Variant report

Variant	rs35972236
Chromosome Location	chr8:64759682-64759683
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]
rs11777464	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12674936	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12675356	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1356988	1.00[ASN][1000 genomes]
rs1520922	0.83[AMR][1000 genomes]
rs16919009	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17217477	1.00[ASN][1000 genomes]
rs17217512	0.97[AMR][1000 genomes]
rs7829551	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7832628	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64757800-64762400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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