Variant report

Variant	rs72959958
Chromosome Location	chr4:149845946-149845947
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10010253	1.00[AMR][1000 genomes]
rs10012689	1.00[AMR][1000 genomes]
rs28633438	1.00[AMR][1000 genomes]
rs28664899	1.00[AMR][1000 genomes]
rs56973742	1.00[AMR][1000 genomes]
rs59323238	1.00[AMR][1000 genomes]
rs59647681	1.00[AMR][1000 genomes]
rs60112920	1.00[AMR][1000 genomes]
rs72950440	1.00[AMR][1000 genomes]
rs72950468	1.00[AMR][1000 genomes]
rs72950497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72959921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72959938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72959947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72959954	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72959983	1.00[AMR][1000 genomes]
rs72959992	1.00[AMR][1000 genomes]
rs72963090	1.00[AMR][1000 genomes]
rs72965114	1.00[AMR][1000 genomes]
rs72965118	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	nsv461677	chr4:149794284-149903982	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv595686	chr4:149794284-149903982	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv470083	chr4:149817052-149903982	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149845600-149846200	Enhancers	Stomach Smooth Muscle	stomach
2	chr4:149845600-149847800	Weak transcription	Stomach Mucosa	stomach
3	chr4:149845800-149846000	Enhancers	Fetal Stomach	stomach

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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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