Variant report

Variant	rs915064
Chromosome Location	chr14:63177577-63177578
allele	A/G
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]
rs10131119	0.90[EUR][1000 genomes]
rs1032306	1.00[CEU][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10873162	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11158447	1.00[CEU][hapmap];0.93[AMR][1000 genomes]
rs12372901	1.00[ASN][1000 genomes]
rs2355061	1.00[CEU][hapmap];0.86[GIH][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35651857	1.00[CEU][hapmap]
rs36004050	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7141353	0.85[MKK][hapmap]
rs7141855	0.96[EUR][1000 genomes]
rs7141868	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs915062	0.99[AFR][1000 genomes]
rs915065	0.83[AFR][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	nsv902014	chr14:63137629-63178635	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv527675	chr14:63168547-63211280	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63168200-63182400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:63168400-63177800	Weak transcription	hESC Derived CD56+ Ectoderm 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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