Variant report

Variant	rs1833766
Chromosome Location	chr5:147660725-147660726
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10053194	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1432687	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1432691	0.97[ASN][1000 genomes]
rs4367290	0.99[ASN][1000 genomes]
rs4513684	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs56688181	0.95[ASN][1000 genomes]
rs56829637	0.99[ASN][1000 genomes]
rs60697678	0.99[ASN][1000 genomes]
rs61028975	0.99[ASN][1000 genomes]
rs6861777	0.99[ASN][1000 genomes]
rs6865938	0.97[ASN][1000 genomes]
rs6887885	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs73795076	0.99[ASN][1000 genomes]
rs7707656	0.97[ASN][1000 genomes]
rs7707813	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7709159	0.81[ASN][1000 genomes]
rs7713202	0.99[ASN][1000 genomes]
rs7724380	0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv883016	chr5:147640718-147689700	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv883017	chr5:147640718-147689700	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv883018	chr5:147640718-147691470	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv462479	chr5:147648510-147688035	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv599943	chr5:147648510-147688035	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv462480	chr5:147648510-147689700	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv599944	chr5:147648510-147689700	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv883019	chr5:147648750-147689700	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv883020	chr5:147649181-147688035	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv599945	chr5:147649181-147720487	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147648600-147661400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:147658800-147663200	Weak transcription	Hela-S3	cervix
3	chr5:147659800-147661200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:147660000-147661200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr5:147660000-147661200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:147660200-147661200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr5:147660200-147661200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:147660200-147661600	Enhancers	Stomach Mucosa	stomach
9	chr5:147660200-147669400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr5:147660400-147660800	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr5:147660400-147661000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:147660400-147661200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:147660600-147661200	Enhancers	Lung	lung
14	chr5:147660600-147661600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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