Variant report

Variant	rs385712
Chromosome Location	chr21:41492045-41492046
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16999315	1.00[EUR][1000 genomes]
rs16999332	1.00[EUR][1000 genomes]
rs16999336	1.00[EUR][1000 genomes]
rs16999355	1.00[EUR][1000 genomes]
rs2837449	1.00[JPT][hapmap];0.84[YRI][hapmap];0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2837457	1.00[JPT][hapmap];0.84[YRI][hapmap];1.00[EUR][1000 genomes]
rs389575	0.92[AFR][1000 genomes]
rs430434	0.82[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs451518	0.92[AFR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41488600-41493600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr21:41491800-41510200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

Quick Search:

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

what's new

Quick links