Variant report

Variant	rs73133598
Chromosome Location	chr1:225334972-225334973
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs73129886	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73131794	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133528	1.00[AMR][1000 genomes]
rs73133596	1.00[AMR][1000 genomes]
rs73135004	1.00[AMR][1000 genomes]
rs73135007	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73135009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73135016	1.00[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	nsv873225	chr1:225162060-225373936	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv998899	chr1:225210813-225496353	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv524461	chr1:225304331-225347689	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv468205	chr1:225304971-225476025	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv549264	chr1:225304971-225476025	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225301800-225355800	Weak transcription	Pancreas	Pancrea
2	chr1:225322000-225356000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:225326400-225355800	Weak transcription	Ovary	ovary
4	chr1:225326600-225336200	Weak transcription	Fetal Intestine Small	intestine
5	chr1:225331000-225339200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:225332800-225356000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:225334200-225343400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:225334600-225338600	Weak transcription	Fetal Muscle Leg	muscle
9	chr1:225334600-225339200	Weak transcription	HUES48 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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