Variant report

Variant	rs10939917
Chromosome Location	chr5:61134208-61134209
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10059717	1.00[ASN][1000 genomes]
rs10939916	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11748712	1.00[ASN][1000 genomes]
rs12515900	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16895755	0.85[ASN][1000 genomes]
rs1995273	1.00[ASN][1000 genomes]
rs2055380	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2197509	1.00[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs55916023	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72765230	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72765242	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[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	chr5:61130200-61162000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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