Variant report

Variant	rs72935499
Chromosome Location	chr1:73320005-73320006
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1525983	1.00[EUR][1000 genomes]
rs1526003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2462726	1.00[EUR][1000 genomes]
rs2462728	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2494757	1.00[EUR][1000 genomes]
rs2494758	1.00[EUR][1000 genomes]
rs2692846	1.00[EUR][1000 genomes]
rs2692861	1.00[EUR][1000 genomes]
rs2692872	1.00[EUR][1000 genomes]
rs2841183	1.00[EUR][1000 genomes]
rs2841193	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4606265	1.00[EUR][1000 genomes]
rs6679157	1.00[EUR][1000 genomes]
rs74092234	1.00[EUR][1000 genomes]
rs940916	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv1013549	chr1:73209040-73408373	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014200	chr1:73310043-73345847	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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