Variant report

Variant	rs73752214
Chromosome Location	chr5:41683830-41683831
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12109484	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55957622	0.81[AMR][1000 genomes]
rs56347183	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57536348	0.81[AMR][1000 genomes]
rs57555512	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58511292	0.81[AMR][1000 genomes]
rs58783539	0.81[AMR][1000 genomes]
rs59074523	0.81[AMR][1000 genomes]
rs59194359	0.81[AMR][1000 genomes]
rs59365840	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59421702	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs59857800	0.84[AMR][1000 genomes]
rs60432772	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60491534	0.81[AMR][1000 genomes]
rs61303374	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6873842	0.81[AMR][1000 genomes]
rs6876042	0.81[AMR][1000 genomes]
rs6897007	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73076205	0.81[AMR][1000 genomes]
rs73076279	0.81[AMR][1000 genomes]
rs73078212	0.81[AMR][1000 genomes]
rs73087787	0.81[AMR][1000 genomes]
rs73089508	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73752207	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41678800-41685400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:41683000-41684200	Enhancers	hESC Derived CD184+ Endoderm 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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