Variant report

Variant	rs705988
Chromosome Location	chr8:64743305-64743306
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12543529	0.85[ASN][1000 genomes]
rs12545994	0.80[EUR][1000 genomes]
rs12547897	0.80[EUR][1000 genomes]
rs12550178	0.85[EUR][1000 genomes]
rs12675807	0.91[ASN][1000 genomes]
rs12680276	0.80[EUR][1000 genomes]
rs13254613	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1520917	0.85[EUR][1000 genomes]
rs1520930	0.81[ASN][1000 genomes]
rs16930666	0.83[EUR][1000 genomes]
rs1985894	0.85[ASN][1000 genomes]
rs2217020	0.85[EUR][1000 genomes]
rs4737186	0.85[EUR][1000 genomes]
rs4737187	0.84[EUR][1000 genomes]
rs4737661	0.85[ASN][1000 genomes]
rs6982653	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6988399	0.85[ASN][1000 genomes]
rs6994250	0.91[ASN][1000 genomes]
rs705990	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64741000-64744200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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