Variant report

Variant	rs868578
Chromosome Location	chr4:147819677-147819678
allele	A/G
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]
rs12501579	0.81[AMR][1000 genomes]
rs17609956	0.81[AMR][1000 genomes]
rs17656106	0.81[AMR][1000 genomes]
rs2043704	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35788629	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3810845	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4835060	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4835353	0.85[AMR][1000 genomes]
rs68011593	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6855967	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs72943815	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72960363	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72960364	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147817800-147820800	Weak transcription	H1 Derived Mesenchymal Stem 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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