Variant report

Variant	rs1586649
Chromosome Location	chr14:63256420-63256421
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:14)

rs_ID	r²[population]
rs11158454	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11846728	0.85[ASN][1000 genomes]
rs12436815	0.88[CEU][hapmap];0.92[EUR][1000 genomes]
rs12883427	0.86[ASN][1000 genomes]
rs1475743	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs1475744	0.82[ASN][1000 genomes]
rs1810976	0.88[ASN][1000 genomes]
rs1884509	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs2015340	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4902186	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs4902187	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs8010200	0.83[CEU][hapmap]
rs8014674	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8016650	0.97[ASN][1000 genomes]

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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