Variant report

Variant	rs72657186
Chromosome Location	chr8:58605167-58605168
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs28857234	0.88[EUR][1000 genomes]
rs28894753	0.88[EUR][1000 genomes]
rs36156385	0.88[EUR][1000 genomes]
rs55682750	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55718924	0.90[EUR][1000 genomes]
rs56147716	0.81[EUR][1000 genomes]
rs56259251	0.95[EUR][1000 genomes]
rs57456024	0.88[EUR][1000 genomes]
rs58625384	0.85[EUR][1000 genomes]
rs61193147	0.90[EUR][1000 genomes]
rs6471635	0.88[EUR][1000 genomes]
rs6986591	0.85[EUR][1000 genomes]
rs6992409	0.95[EUR][1000 genomes]
rs7003082	0.88[EUR][1000 genomes]
rs7012716	0.95[EUR][1000 genomes]
rs72657140	0.88[EUR][1000 genomes]
rs72657151	0.88[EUR][1000 genomes]
rs72657154	0.88[EUR][1000 genomes]
rs72657161	0.85[EUR][1000 genomes]
rs72657163	0.88[EUR][1000 genomes]
rs72657165	0.88[EUR][1000 genomes]
rs72657168	0.90[EUR][1000 genomes]
rs72657185	0.97[EUR][1000 genomes]
rs72657189	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72659115	0.85[EUR][1000 genomes]
rs72659116	0.85[EUR][1000 genomes]
rs72659120	0.85[EUR][1000 genomes]
rs72659121	0.85[EUR][1000 genomes]
rs72659122	0.85[EUR][1000 genomes]
rs72659131	0.85[EUR][1000 genomes]
rs72659132	0.85[EUR][1000 genomes]
rs72659133	0.83[EUR][1000 genomes]
rs72659134	0.85[EUR][1000 genomes]
rs72659138	0.80[EUR][1000 genomes]
rs7825239	0.88[EUR][1000 genomes]
rs7831758	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	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv890937	chr8:58600994-58695807	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58602000-58616200	Weak transcription	Aorta	Aorta
2	chr8:58603200-58606400	Weak transcription	Pancreas	Pancrea

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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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