Variant report

Variant	rs73541324
Chromosome Location	chr9:98103686-98103687
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1800363	1.00[AMR][1000 genomes]
rs4647423	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4647425	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4647452	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4647499	1.00[AMR][1000 genomes]
rs4647500	1.00[AMR][1000 genomes]
rs4647541	1.00[AMR][1000 genomes]
rs4647545	1.00[AMR][1000 genomes]
rs56769237	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59061676	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59172564	1.00[AMR][1000 genomes]
rs59985123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73528471	1.00[AMR][1000 genomes]
rs73528483	1.00[AMR][1000 genomes]
rs73532163	1.00[AMR][1000 genomes]
rs73532166	1.00[AMR][1000 genomes]
rs73532168	1.00[AMR][1000 genomes]
rs73532171	1.00[AMR][1000 genomes]
rs73532182	1.00[AMR][1000 genomes]
rs73532183	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73534866	1.00[AMR][1000 genomes]
rs73534884	1.00[AMR][1000 genomes]
rs73537206	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73537207	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73537294	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73539206	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73539218	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73541317	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73541318	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73541320	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73541321	0.81[AFR][1000 genomes]
rs7848866	1.00[AMR][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	nsv831657	chr9:97959274-98204769	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv531633	chr9:98078300-98431120	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv3330996	chr9:98083446-98112507	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 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	chr9:98099600-98105000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:98101000-98105000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:98102600-98104200	Enhancers	Fetal Lung	lung
4	chr9:98103200-98104200	Enhancers	Fetal Stomach	stomach
5	chr9:98103200-98104200	Enhancers	Ovary	ovary
6	chr9:98103200-98104200	Enhancers	HSMMtube	muscle
7	chr9:98103600-98104000	Enhancers	Right Atrium	heart
8	chr9:98103600-98105400	Enhancers	Fetal Heart	heart

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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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