Variant report

Variant	rs4142777
Chromosome Location	chr16:48722062-48722063
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11076574	0.84[AMR][1000 genomes]
rs12443883	1.00[CEU][hapmap];0.93[CHB][hapmap]
rs12597314	0.84[EUR][1000 genomes]
rs16946440	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906047	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4785522	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[YRI][hapmap]
rs4785523	1.00[CEU][hapmap];0.93[CHB][hapmap]
rs4785524	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.80[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48721600-48723200	Enhancers	HUES64 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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