Variant report

Variant	rs58900215
Chromosome Location	chr14:63366992-63366993
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17100517	0.89[AMR][1000 genomes]
rs17100546	0.87[AMR][1000 genomes]
rs17100551	1.00[AMR][1000 genomes]
rs17100561	1.00[AMR][1000 genomes]
rs17100564	0.89[AMR][1000 genomes]
rs17100566	0.89[AMR][1000 genomes]
rs56677467	0.87[AMR][1000 genomes]
rs7157114	0.89[AMR][1000 genomes]
rs73276452	0.89[AMR][1000 genomes]
rs73276489	0.89[AMR][1000 genomes]
rs8018130	1.00[AMR][1000 genomes]
rs8019319	1.00[AMR][1000 genomes]
rs8019870	0.89[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	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	chr14:63364000-63369200	Weak transcription	H1 Cell Line	embryonic stem cell

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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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