Variant report

Variant	rs73455324
Chromosome Location	chr7:137303301-137303302
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11971016	1.00[AMR][1000 genomes]
rs3778784	1.00[AMR][1000 genomes]
rs3778787	1.00[AMR][1000 genomes]
rs58245080	1.00[AMR][1000 genomes]
rs58503212	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs59626548	0.83[AMR][1000 genomes]
rs59811187	1.00[AMR][1000 genomes]
rs73455308	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73461023	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73461041	1.00[AMR][1000 genomes]
rs73461053	1.00[AMR][1000 genomes]
rs73461054	1.00[AMR][1000 genomes]
rs73461063	1.00[AMR][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	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
3	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	esv1812888	chr7:137283212-137366467	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137277200-137326800	Weak transcription	Osteobl	bone
2	chr7:137277400-137312000	Weak transcription	Brain Angular Gyrus	brain
3	chr7:137277600-137315400	Weak transcription	NH-A	brain
4	chr7:137278400-137304200	Weak transcription	Aorta	Aorta
5	chr7:137282800-137337400	Weak transcription	HSMMtube	muscle
6	chr7:137288000-137310800	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:137294000-137328400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:137296600-137308200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:137297600-137311400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:137297600-137324200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr7:137302600-137303400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:137303000-137304600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:137303200-137304400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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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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