Variant report

Variant	rs73650737
Chromosome Location	chr9:85195363-85195364
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs7022118	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73650739	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73650741	0.85[AFR][1000 genomes]
rs7857463	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7875519	0.99[AFR][1000 genomes]
rs7875637	0.99[AFR][1000 genomes]
rs9919047	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 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	chr9:85195200-85195400	Enhancers	Pancreas	Pancrea
2	chr9:85195200-85195400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr9:85195200-85195600	Flanking Active TSS	Liver	Liver
4	chr9:85195200-85195600	Flanking Active TSS	HepG2	liver
5	chr9:85195200-85196600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr9:85195200-85196600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr9:85195200-85198200	Enhancers	Fetal Intestine Small	intestine
8	chr9:85195200-85205000	Enhancers	Fetal Intestine Large	intestine

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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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