Variant report

Variant	rs10515378
Chromosome Location	chr5:107129158-107129159
allele	C/T
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:12)

rs_ID	r²[population]
rs10054885	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10061482	0.94[EUR][1000 genomes]
rs10479410	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11738855	0.93[EUR][1000 genomes]
rs11739903	0.94[EUR][1000 genomes]
rs11739995	0.94[EUR][1000 genomes]
rs1422436	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34813961	0.94[EUR][1000 genomes]
rs35762765	0.94[EUR][1000 genomes]
rs6888213	0.94[EUR][1000 genomes]
rs72795904	0.94[EUR][1000 genomes]
rs72795909	0.93[EUR][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	nsv830440	chr5:107074116-107278905	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:107127800-107135400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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