Variant report

Variant	rs58987310
Chromosome Location	chr2:76512784-76512785
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10865419	0.93[ASN][1000 genomes]
rs11887752	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12615757	0.94[ASN][1000 genomes]
rs12616451	0.98[AMR][1000 genomes]
rs12622814	0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1526624	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1526644	0.93[ASN][1000 genomes]
rs17012424	0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17012428	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs17012430	0.97[ASN][1000 genomes]
rs17012485	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4852400	0.83[AFR][1000 genomes];0.97[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	chr2:76508800-76520200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:76509600-76515200	Weak transcription	H9 Derived Neuronal Progenitor Cultured 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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