Variant report

Variant	rs7493979
Chromosome Location	chr14:63270269-63270270
allele	C/G
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]
rs1021346	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10483756	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs11158452	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs12433281	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12891322	0.88[ASN][1000 genomes]
rs12891982	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12893269	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12897538	0.80[CHB][hapmap];0.88[JPT][hapmap]
rs17834917	0.81[CEU][hapmap];0.88[JPT][hapmap]
rs2171876	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35679534	0.82[EUR][1000 genomes]
rs56397364	0.91[ASN][1000 genomes]
rs961066	1.00[CEU][hapmap];0.82[AMR][1000 genomes];1.00[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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63255600-63274400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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