Variant report

Variant	rs72921166
Chromosome Location	chr4:125406231-125406232
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13107808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13117687	1.00[AMR][1000 genomes]
rs13141054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13141440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13143594	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17008239	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17008257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs188739	0.84[EUR][1000 genomes]
rs312488	0.84[EUR][1000 genomes]
rs312490	0.84[EUR][1000 genomes]
rs34487884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34930933	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35660686	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71608189	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72921170	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72921179	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72921182	0.89[AFR][1000 genomes]
rs72921187	0.89[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	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv879880	chr4:125174817-125494547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2760890	chr4:125273456-125466931	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv879881	chr4:125280852-125448288	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125404800-125410000	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:125404800-125412600	Weak transcription	Fetal Stomach	stomach
3	chr4:125405000-125411200	Weak transcription	Fetal Heart	heart
4	chr4:125405200-125406400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:125405400-125409000	Weak transcription	Brain Germinal Matrix	brain
6	chr4:125405400-125410400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:125405600-125408400	Weak transcription	Fetal Lung	lung
8	chr4:125406000-125406400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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