Variant report

Variant	rs72932392
Chromosome Location	chr1:69959030-69959031
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs59878053	1.00[AFR][1000 genomes]
rs72932368	1.00[AMR][1000 genomes]
rs72932371	1.00[AMR][1000 genomes]
rs72932373	1.00[AMR][1000 genomes]
rs72932386	1.00[AMR][1000 genomes]
rs72932387	1.00[AMR][1000 genomes]
rs72932395	1.00[AMR][1000 genomes]
rs72932399	1.00[AMR][1000 genomes]
rs72934438	1.00[AFR][1000 genomes]
rs72934459	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	nsv949691	chr1:69749722-70302201	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv870931	chr1:69765592-69959061	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3384194	chr1:69885024-70275430	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv546451	chr1:69894849-69975660	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69957000-69959600	Enhancers	NH-A	brain
2	chr1:69957200-69961200	Enhancers	NHEK	skin
3	chr1:69957400-69960800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:69957400-69960800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:69957400-69960800	Enhancers	HMEC	breast
6	chr1:69958000-69960800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:69958800-69959600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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