Variant report

Variant	rs12920938
Chromosome Location	chr16:47759781-47759782
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1200969	0.80[AFR][1000 genomes]
rs2098420	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2342693	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs41427947	1.00[EUR][1000 genomes]
rs41438546	1.00[EUR][1000 genomes]
rs55915748	1.00[EUR][1000 genomes]
rs56026849	1.00[EUR][1000 genomes]
rs58917857	1.00[EUR][1000 genomes]
rs60269785	1.00[EUR][1000 genomes]
rs61075689	1.00[EUR][1000 genomes]
rs61351980	1.00[EUR][1000 genomes]
rs7187698	1.00[EUR][1000 genomes]
rs74016219	1.00[EUR][1000 genomes]
rs74016220	1.00[EUR][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	nsv520355	chr16:47424828-48164777	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv525976	chr16:47583872-48035026	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv428657	chr16:47748036-47913816	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47753400-47760000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:47755400-47765400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr16:47756400-47761800	Weak transcription	Stomach Mucosa	stomach
4	chr16:47758000-47763600	Weak transcription	Fetal Brain Male	brain

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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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