Variant report

Variant	rs73296865
Chromosome Location	chr8:85273798-85273799
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs16912697	1.00[AMR][1000 genomes]
rs59415044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73291385	1.00[AMR][1000 genomes]
rs73291389	1.00[AMR][1000 genomes]
rs73291396	1.00[AMR][1000 genomes]
rs73291399	1.00[AMR][1000 genomes]
rs73293026	1.00[AMR][1000 genomes]
rs73293085	1.00[AMR][1000 genomes]
rs73293089	1.00[AMR][1000 genomes]
rs73293091	1.00[AMR][1000 genomes]
rs73293096	1.00[AMR][1000 genomes]
rs73293097	1.00[AMR][1000 genomes]
rs73293100	1.00[AMR][1000 genomes]
rs73293101	1.00[AMR][1000 genomes]
rs73294894	1.00[AMR][1000 genomes]
rs73294897	1.00[AMR][1000 genomes]
rs73294938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73294940	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73296724	1.00[AMR][1000 genomes]
rs73296860	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73299826	1.00[AMR][1000 genomes]
rs73299828	1.00[AMR][1000 genomes]
rs73299831	1.00[AMR][1000 genomes]
rs73304840	1.00[AMR][1000 genomes]
rs73304860	1.00[AMR][1000 genomes]
rs73304870	1.00[AMR][1000 genomes]
rs73304881	1.00[AMR][1000 genomes]
rs73304882	1.00[AMR][1000 genomes]
rs73304884	1.00[AMR][1000 genomes]
rs73306919	1.00[AMR][1000 genomes]
rs73306938	1.00[AMR][1000 genomes]
rs73306940	1.00[AMR][1000 genomes]
rs73306942	1.00[AMR][1000 genomes]
rs73306944	1.00[AMR][1000 genomes]
rs73306952	1.00[AMR][1000 genomes]
rs73306956	1.00[AMR][1000 genomes]
rs73306959	1.00[AMR][1000 genomes]
rs73306964	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831374	chr8:85103604-85308976	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv1806721	chr8:85257984-85274061	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv831375	chr8:85272352-85463621	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85273400-85274200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr8:85273600-85274000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:85273600-85274200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell 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