Variant report

Variant	rs73735402
Chromosome Location	chr6:45350478-45350479
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs55944527	0.83[AFR][1000 genomes]
rs56007105	0.83[AFR][1000 genomes]
rs56166696	0.83[AFR][1000 genomes]
rs56389859	0.83[AFR][1000 genomes]
rs60756874	0.83[AFR][1000 genomes]
rs73735305	0.83[AFR][1000 genomes]
rs73735306	0.83[AFR][1000 genomes]
rs73735311	0.83[AFR][1000 genomes]
rs73735312	0.83[AFR][1000 genomes]
rs73735326	0.83[AFR][1000 genomes]
rs73735331	0.83[AFR][1000 genomes]
rs73735333	0.83[AFR][1000 genomes]
rs73735334	0.83[AFR][1000 genomes]
rs73735350	0.83[AFR][1000 genomes]
rs73735355	0.83[AFR][1000 genomes]
rs73735371	0.83[AFR][1000 genomes]
rs73735372	0.83[AFR][1000 genomes]
rs73735377	0.83[AFR][1000 genomes]
rs73735379	0.83[AFR][1000 genomes]
rs73737404	0.83[AFR][1000 genomes]
rs73737406	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 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	chr6:45346400-45351400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr6:45347000-45355000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:45347200-45354200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr6:45347400-45350600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:45349400-45351200	Enhancers	Placenta	Placenta
6	chr6:45349800-45350600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:45349800-45350800	Enhancers	Placenta Amnion	Placenta Amnion

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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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