Variant report

Variant	rs73513785
Chromosome Location	chr9:110027761-110027762
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11573621	1.00[EUR][1000 genomes]
rs11573630	1.00[EUR][1000 genomes]
rs11573634	1.00[EUR][1000 genomes]
rs11573647	1.00[EUR][1000 genomes]
rs11573650	1.00[EUR][1000 genomes]
rs11573653	1.00[EUR][1000 genomes]
rs11573666	1.00[EUR][1000 genomes]
rs11573667	1.00[EUR][1000 genomes]
rs16912336	1.00[EUR][1000 genomes]
rs1805260	1.00[EUR][1000 genomes]
rs57392585	1.00[EUR][1000 genomes]
rs57474128	1.00[EUR][1000 genomes]
rs58248414	1.00[EUR][1000 genomes]
rs58465981	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59581003	1.00[EUR][1000 genomes]
rs60306961	1.00[EUR][1000 genomes]
rs60677048	1.00[EUR][1000 genomes]
rs61015686	1.00[EUR][1000 genomes]
rs7020515	1.00[EUR][1000 genomes]
rs7024037	1.00[EUR][1000 genomes]
rs73509835	1.00[EUR][1000 genomes]
rs73509843	1.00[EUR][1000 genomes]
rs73509845	1.00[EUR][1000 genomes]
rs73513774	1.00[EUR][1000 genomes]
rs73513780	1.00[EUR][1000 genomes]
rs73513790	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73515722	1.00[EUR][1000 genomes]
rs73515802	1.00[EUR][1000 genomes]
rs73668770	1.00[EUR][1000 genomes]
rs7847357	1.00[EUR][1000 genomes]
rs7855013	1.00[EUR][1000 genomes]
rs7861622	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869351	chr9:109593212-110191170	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv831682	chr9:109937181-110075453	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv893698	chr9:109998563-110052660	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv508560	chr9:110006490-110060539	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110023400-110028800	Weak transcription	HMEC	breast
2	chr9:110023400-110031400	Weak transcription	A549	lung
3	chr9:110023800-110029000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:110023800-110031600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:110023800-110031600	Weak transcription	Placenta	Placenta
6	chr9:110023800-110031600	Weak transcription	HSMMtube	muscle
7	chr9:110024000-110031600	Weak transcription	NHDF-Ad	bronchial
8	chr9:110025800-110029000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr9:110026200-110028800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:110027400-110028200	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr9:110027600-110027800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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