Variant report

Variant	rs1862310
Chromosome Location	chr5:107125801-107125802
allele	C/T
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]
rs10037033	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10045237	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10057444	0.84[ASN][1000 genomes]
rs11242650	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12516234	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12518562	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12522401	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28539291	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6869199	0.85[ASN][1000 genomes]
rs6875281	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6875450	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6876584	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs930219	0.93[ASN][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	chr5:107125800-107126200	ZNF genes & repeats	Fetal Heart	heart

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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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