Variant report

Variant	rs59475005
Chromosome Location	chr9:93317866-93317867
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10116374	0.98[ASN][1000 genomes]
rs12682759	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12682906	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12685637	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41281206	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57309876	1.00[AMR][1000 genomes]
rs58297912	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60703181	1.00[AMR][1000 genomes]
rs60852050	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61012080	1.00[AMR][1000 genomes]
rs61263953	1.00[AMR][1000 genomes]
rs61559611	1.00[AMR][1000 genomes]
rs7860821	0.98[ASN][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	nsv1041278	chr9:92965701-93560454	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv893565	chr9:93130796-93392332	Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv893566	chr9:93209923-93439259	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr9:93309800-93319400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:93315600-93321000	Weak transcription	GM12878-XiMat	blood
3	chr9:93317000-93318400	Enhancers	Stomach Mucosa	stomach
4	chr9:93317000-93318600	Enhancers	Liver	Liver
5	chr9:93317200-93318400	Enhancers	Gastric	stomach
6	chr9:93317200-93318400	Enhancers	Pancreas	Pancrea
7	chr9:93317200-93319600	Enhancers	HepG2	liver
8	chr9:93317400-93318000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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