Variant report

Variant	rs1682452
Chromosome Location	chr2:184657831-184657832
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1682427	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs826170	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs826174	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs826175	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs826176	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs826177	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184657800-184658400	Weak transcription	ES-UCSF4 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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