Variant report

Variant	rs16933728
Chromosome Location	chr9:15885733-15885734
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:11)

rs_ID	r²[population]
rs10738419	0.86[YRI][hapmap]
rs12001446	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12002304	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12005527	1.00[AMR][1000 genomes]
rs12006236	0.82[ASW][hapmap];0.90[LWK][hapmap];0.85[YRI][hapmap];0.87[AFR][1000 genomes]
rs16933677	1.00[AMR][1000 genomes]
rs16933746	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16933756	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16933851	1.00[AMR][1000 genomes]
rs16933881	1.00[AMR][1000 genomes]
rs16933886	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15877000-15903400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:15877400-15885800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:15877600-15888400	Weak transcription	Pancreas	Pancrea
4	chr9:15884200-15891800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr9:15884200-15892200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:15885400-15885800	Strong transcription	Primary hematopoietic stem cells	blood
7	chr9:15885400-15886800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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