Variant report

Variant	rs73653209
Chromosome Location	chr9:79396500-79396501
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs4317645	1.00[EUR][1000 genomes]
rs6560543	0.85[EUR][1000 genomes]
rs7026661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7036892	0.85[EUR][1000 genomes]
rs73653212	0.85[EUR][1000 genomes]
rs7862512	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1040363	chr9:79246366-79711737	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv2758190	chr9:79365865-79673907	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv2759697	chr9:79365865-79673907	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79361200-79396600	Weak transcription	Aorta	Aorta
2	chr9:79371600-79400200	Weak transcription	HSMMtube	muscle
3	chr9:79377000-79408600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:79377200-79405200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr9:79388000-79401400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:79388200-79398200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr9:79388200-79403400	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:79388400-79397600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:79388400-79398200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:79388600-79399000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:79389000-79399400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr9:79393400-79401800	Weak transcription	Brain Hippocampus Middle	brain
13	chr9:79393600-79401200	Weak transcription	Brain Substantia Nigra	brain
14	chr9:79393600-79423400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr9:79394000-79397600	Weak transcription	HSMM	muscle
16	chr9:79395200-79403400	Weak transcription	Fetal Intestine Small	intestine
17	chr9:79396400-79402400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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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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