Variant report

Variant	rs73502933
Chromosome Location	chr9:104431379-104431380
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10114871	0.86[AFR][1000 genomes]
rs10117050	0.87[AFR][1000 genomes]
rs10119079	0.87[AFR][1000 genomes]
rs10119283	0.82[AFR][1000 genomes]
rs10120736	0.82[AFR][1000 genomes]
rs10121691	0.82[AFR][1000 genomes]
rs10122077	0.87[AFR][1000 genomes]
rs10123334	0.87[AFR][1000 genomes]
rs10125809	1.00[AFR][1000 genomes]
rs10156603	0.87[AFR][1000 genomes]
rs10989575	1.00[AFR][1000 genomes]
rs10989593	0.87[AFR][1000 genomes]
rs11506966	1.00[AFR][1000 genomes]
rs12339890	0.82[AFR][1000 genomes]
rs12340167	1.00[AFR][1000 genomes]
rs12342952	0.87[AFR][1000 genomes]
rs12343034	0.82[AFR][1000 genomes]
rs12343188	1.00[AFR][1000 genomes]
rs12344042	1.00[AFR][1000 genomes]
rs12344841	1.00[AFR][1000 genomes]
rs12346815	1.00[AFR][1000 genomes]
rs28420755	1.00[AFR][1000 genomes]
rs28436645	0.87[AFR][1000 genomes]
rs28456110	0.82[AFR][1000 genomes]
rs28504973	0.86[AFR][1000 genomes]
rs28612816	1.00[AFR][1000 genomes]
rs28621686	1.00[AFR][1000 genomes]
rs28631285	0.82[AFR][1000 genomes]
rs28680751	0.87[AFR][1000 genomes]
rs28687945	1.00[AFR][1000 genomes]
rs28736781	0.87[AFR][1000 genomes]
rs58800610	0.82[AFR][1000 genomes]
rs73496772	1.00[AFR][1000 genomes]
rs73504933	0.82[AFR][1000 genomes]
rs73504976	0.82[AFR][1000 genomes]
rs73658427	1.00[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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104425800-104436000	Weak transcription	Liver	Liver
2	chr9:104429800-104431800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:104430400-104431400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr9:104430600-104431600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:104430600-104431800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:104431000-104431600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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