Variant report

Variant	rs73332229
Chromosome Location	chr8:125118794-125118795
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:8)

rs_ID	r²[population]
rs56967015	1.00[AFR][1000 genomes]
rs57182710	1.00[AFR][1000 genomes]
rs73328367	0.88[AFR][1000 genomes]
rs73328376	1.00[AFR][1000 genomes]
rs73330113	0.94[AFR][1000 genomes]
rs73330167	0.89[AFR][1000 genomes]
rs73330200	1.00[AFR][1000 genomes]
rs73332208	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612144	chr8:125057728-125206503	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1023183	chr8:125060532-125206445	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv948556	chr8:125067187-125204721	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv831452	chr8:125099708-125259926	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125076800-125121800	Weak transcription	Fetal Stomach	stomach
2	chr8:125100800-125124600	Weak transcription	Gastric	stomach
3	chr8:125116200-125121400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:125117000-125120200	Weak transcription	HepG2	liver
5	chr8:125117600-125119600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:125117600-125124200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:125117800-125118800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:125117800-125118800	Weak transcription	Fetal Intestine Small	intestine
9	chr8:125117800-125119800	Weak transcription	Fetal Intestine Large	intestine
10	chr8:125117800-125121400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:125118000-125119200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:125118200-125118800	Weak transcription	Stomach Mucosa	stomach

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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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