Variant report

Variant	rs11764429
Chromosome Location	chr7:96929932-96929933
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10486857	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11972340	0.84[ASN][1000 genomes]
rs12538310	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1420174	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1476601	0.82[ASN][1000 genomes]
rs2014018	0.84[ASN][1000 genomes]
rs2158498	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28369152	0.84[ASN][1000 genomes]
rs28413832	0.84[ASN][1000 genomes]
rs73238872	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73238878	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73392167	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs878502	0.84[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96929800-96930000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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