Variant report

Variant	rs10145113
Chromosome Location	chr14:84673997-84673998
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11159634	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11159635	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12590599	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12590626	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12590652	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12590669	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1676065	0.93[EUR][1000 genomes]
rs1779579	0.93[EUR][1000 genomes]
rs2045739	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2045740	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58632727	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67304290	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157123	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7157150	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72629343	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72629346	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72629347	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72629348	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72629351	0.93[EUR][1000 genomes];0.92[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	nsv976854	chr14:84667225-84675082	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84673600-84674600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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