Variant report

Variant	rs58440806
Chromosome Location	chr4:143867890-143867891
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10213146	1.00[AMR][1000 genomes]
rs13434730	0.91[AFR][1000 genomes]
rs28582179	0.93[AFR][1000 genomes]
rs28733456	1.00[AMR][1000 genomes]
rs72935935	1.00[AMR][1000 genomes]
rs72939952	0.91[AFR][1000 genomes]
rs72944026	1.00[AMR][1000 genomes]
rs72944063	1.00[AMR][1000 genomes]
rs72944065	1.00[AMR][1000 genomes]
rs72952048	1.00[AMR][1000 genomes]
rs7662099	1.00[AMR][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	nsv880175	chr4:143779613-143892252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830102	chr4:143820268-143953611	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143866400-143868000	Enhancers	Fetal Muscle Leg	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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