Variant report

Variant	rs72754327
Chromosome Location	chr5:30220441-30220442
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11743556	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12186365	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12186524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12188471	0.84[EUR][1000 genomes]
rs12188709	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17592394	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17652083	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17652137	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34208847	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3924075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4311426	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4867030	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4867254	0.85[EUR][1000 genomes]
rs56410637	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6859904	0.84[EUR][1000 genomes]
rs6870433	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6884693	0.84[EUR][1000 genomes]
rs72752395	0.84[EUR][1000 genomes]
rs72754315	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72754317	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72754323	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72754325	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72754337	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72754350	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72754373	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72754377	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7714947	0.85[EUR][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	nsv881635	chr5:30122190-30371238	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv915858	chr5:30176470-31018294	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:30214800-30223600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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