Variant report

Variant	rs10059717
Chromosome Location	chr5:61169057-61169058
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10062532	0.81[AMR][1000 genomes]
rs10075885	0.81[AMR][1000 genomes]
rs10939916	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939917	1.00[ASN][1000 genomes]
rs11748712	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12515900	1.00[ASN][1000 genomes]
rs1374002	0.83[AMR][1000 genomes]
rs1445875	0.84[MEX][hapmap]
rs16895755	0.85[ASN][1000 genomes]
rs1995273	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1995274	0.83[AMR][1000 genomes]
rs2055380	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2197509	0.96[ASN][1000 genomes]
rs55916023	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72765230	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72765242	0.84[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	nsv1020693	chr5:61098865-61357032	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61168800-61174000	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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