Variant report

Variant	rs73327956
Chromosome Location	chr14:80095838-80095839
allele	A/G
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:10)

rs_ID	r²[population]
rs10147137	0.90[AMR][1000 genomes]
rs28407338	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60570231	0.88[AFR][1000 genomes]
rs6574516	0.81[AMR][1000 genomes]
rs7143533	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7147112	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73329935	0.81[AMR][1000 genomes]
rs8021855	0.90[AMR][1000 genomes]
rs9652380	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9806079	0.84[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	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv869542	chr14:80009619-80118315	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:80095000-80098600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:80095600-80096800	Enhancers	Fetal Kidney	kidney
3	chr14:80095600-80097400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:80095600-80097400	Enhancers	Fetal Intestine Large	intestine
5	chr14:80095800-80096200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:80095800-80096200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:80095800-80096600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:80095800-80097200	Enhancers	Fetal Intestine Small	intestine

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

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