Variant report

Variant	rs4454339
Chromosome Location	chr9:103438905-103438906
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10283519	0.92[ASN][1000 genomes]
rs10283522	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10989206	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10989209	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10989210	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs36196957	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4742790	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4743412	0.91[ASN][1000 genomes]
rs62577640	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103432600-103439200	Enhancers	Fetal Brain Female	brain
2	chr9:103438200-103441400	Weak transcription	Brain Germinal Matrix	brain

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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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