Variant report

Variant	rs73693525
Chromosome Location	chr8:78404088-78404089
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs16919474	1.00[AMR][1000 genomes]
rs16939481	1.00[AMR][1000 genomes]
rs16939483	1.00[AMR][1000 genomes]
rs56177095	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56386822	1.00[AMR][1000 genomes]
rs56766898	1.00[AMR][1000 genomes]
rs58927140	1.00[AMR][1000 genomes]
rs59757211	1.00[AMR][1000 genomes]
rs72435768	1.00[AMR][1000 genomes]
rs73691374	1.00[AMR][1000 genomes]
rs73691629	1.00[AMR][1000 genomes]
rs73691630	1.00[AMR][1000 genomes]
rs73691674	1.00[AMR][1000 genomes]
rs73691675	1.00[AMR][1000 genomes]
rs73691684	1.00[AMR][1000 genomes]
rs73691687	1.00[AMR][1000 genomes]
rs73691688	1.00[AMR][1000 genomes]
rs73693504	1.00[AMR][1000 genomes]
rs73693556	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891045	chr8:77998659-78477561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv891049	chr8:78325885-78565529	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv891050	chr8:78351635-78532763	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv831363	chr8:78367997-78522574	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv891051	chr8:78376314-78477561	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	inside rSNPs	diseases
6	nsv611567	chr8:78387243-78452222	Enhancers ZNF genes & repeats Weak transcription	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:78403600-78404600	Enhancers	H9 Cell Line	embryonic stem cell

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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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