Variant report

Variant	rs73621532
Chromosome Location	chr13:93228711-93228712
allele	A/G
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:11)

rs_ID	r²[population]
rs59816585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73617133	1.00[AMR][1000 genomes]
rs73621519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621527	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621550	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73632249	1.00[AMR][1000 genomes]
rs73632255	1.00[AMR][1000 genomes]
rs73632257	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456070	chr13:93208593-93298523	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv562730	chr13:93208593-93298523	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93226200-93235600	Weak transcription	Right Atrium	heart
2	chr13:93226800-93228800	Enhancers	Fetal Intestine Large	intestine

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