Variant report

Variant	rs2959328
Chromosome Location	chr8:34121810-34121811
allele	A/G
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]
rs1353340	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1495231	0.81[EUR][1000 genomes]
rs1495232	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1495233	0.82[EUR][1000 genomes]
rs1495234	0.82[EUR][1000 genomes]
rs1495235	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1495236	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1994963	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2934978	0.84[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2959329	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2978846	0.82[EUR][1000 genomes]
rs996990	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34119000-34125200	Weak transcription	H1 BMP4 Derived Trophoblast 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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