Variant report

Variant	rs60681214
Chromosome Location	chr9:96568207-96568208
allele	A/G
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]
rs11793318	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2487020	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3209003	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3750462	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4618758	0.83[AFR][1000 genomes]
rs4743935	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7850735	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7855547	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7865953	0.83[EUR][1000 genomes]
rs7869674	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96563800-96569400	Weak transcription	K562	blood
2	chr9:96564400-96569400	Weak transcription	iPS DF 19.11 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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