Variant report

Variant	rs73465558
Chromosome Location	chr9:85547597-85547598
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11139866	1.00[AMR][1000 genomes]
rs17085873	0.89[AFR][1000 genomes]
rs17085881	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17085906	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57671245	0.89[AFR][1000 genomes]
rs58922119	0.89[AFR][1000 genomes]
rs59796082	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59920502	0.89[AFR][1000 genomes]
rs60414804	1.00[AMR][1000 genomes]
rs61210121	1.00[AMR][1000 genomes]
rs73465532	1.00[AFR][1000 genomes]
rs73465565	1.00[AMR][1000 genomes]
rs73465566	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73465577	1.00[AMR][1000 genomes]
rs73465579	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035314	chr9:85348780-85549246	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv540161	chr9:85348780-85549246	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1050771	chr9:85416931-85643417	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893511	chr9:85495968-85833127	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv2603527	chr9:85546269-85547738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85539000-85549600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:85540000-85549400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:85547400-85549800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:85547400-85549800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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