Variant report

Variant	rs9493767
Chromosome Location	chr6:134271827-134271828
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2220134	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73774175	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9483638	0.85[AFR][1000 genomes]
rs9493766	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9493778	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9493782	0.92[AFR][1000 genomes]
rs9493783	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9493784	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9493789	0.92[AFR][1000 genomes];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	esv34122	chr6:134089019-134378252	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv1840176	chr6:134268822-134274297	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
3	esv1838635	chr6:134269008-134273139	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134266600-134272400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:134266800-134272200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:134267000-134272200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:134268400-134272200	Weak transcription	Aorta	Aorta
5	chr6:134268600-134272400	Weak transcription	Fetal Brain Female	brain
6	chr6:134269000-134272400	Weak transcription	K562	blood
7	chr6:134270000-134272400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:134270200-134272400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:134270200-134272400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr6:134270400-134272200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr6:134270400-134272200	Weak transcription	Gastric	stomach
12	chr6:134270400-134272400	Weak transcription	Pancreas	Pancrea
13	chr6:134270600-134272200	Weak transcription	Stomach Mucosa	stomach
14	chr6:134271600-134272000	Weak transcription	Liver	Liver

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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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