Variant report

Variant	rs12936172
Chromosome Location	chr17:50469356-50469357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10515009	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28396077	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4413009	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4474737	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4479297	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4794340	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4794345	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58162778	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72837730	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72837731	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72837735	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72837741	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72837747	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72837748	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8082463	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9892759	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9893828	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492317	chr17:50067819-50774475	Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1064285	chr17:50290372-50507829	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv543385	chr17:50290372-50507829	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv528447	chr17:50323521-51118173	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv428345	chr17:50348160-50511536	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1057173	chr17:50448593-50808216	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2830033	chr17:50462226-50506926	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 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	chr17:50468600-50469400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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