Variant report

Variant	rs4354374
Chromosome Location	chr9:96579385-96579386
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10122041	0.82[CEU][hapmap];0.93[CHB][hapmap];0.82[ASN][1000 genomes]
rs10123836	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10761282	0.81[EUR][1000 genomes]
rs10821229	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13288708	0.81[ASN][1000 genomes]
rs2398874	0.83[ASN][1000 genomes]
rs3957506	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3996254	0.89[ASN][1000 genomes]
rs4075733	0.85[CHB][hapmap]
rs4428726	0.80[ASN][1000 genomes]
rs4744287	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57882762	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7869328	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96577200-96581600	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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