Variant report

Variant	rs73602076
Chromosome Location	chr6:149528870-149528871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs73598083	0.89[AFR][1000 genomes]
rs73598088	0.89[AFR][1000 genomes]
rs73598093	0.89[AFR][1000 genomes]
rs73600006	1.00[AFR][1000 genomes]
rs73600009	0.89[AFR][1000 genomes]
rs73600012	0.89[AFR][1000 genomes]
rs73602011	0.89[AFR][1000 genomes]
rs73602014	0.89[AFR][1000 genomes]
rs73602020	0.89[AFR][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	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149522800-149529000	Weak transcription	Fetal Heart	heart
2	chr6:149523600-149529200	Weak transcription	Brain Germinal Matrix	brain
3	chr6:149524600-149530800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:149525000-149531000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:149528000-149529800	Enhancers	Fetal Lung	lung
6	chr6:149528800-149529000	Enhancers	Stomach Smooth Muscle	stomach
7	chr6:149528800-149529600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:149528800-149530000	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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