Variant report

Variant	rs59347262
Chromosome Location	chr13:62705638-62705639
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17060833	1.00[AFR][1000 genomes]
rs17060843	0.98[AFR][1000 genomes]
rs17060855	1.00[AFR][1000 genomes]
rs17060863	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17060868	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7332531	1.00[EUR][1000 genomes]
rs73505033	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73505042	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73505045	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73505047	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73505049	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73505051	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7998127	1.00[EUR][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	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv832630	chr13:62651865-62811428	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62703400-62706000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:62705200-62708000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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