Variant report

Variant	rs16951022
Chromosome Location	chr16:79721415-79721416
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16951023	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16951025	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16951029	1.00[EUR][1000 genomes]
rs58435964	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59665754	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037513	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037514	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037516	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037517	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037533	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74037534	1.00[EUR][1000 genomes]
rs9652680	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv833295	chr16:79568878-79726768	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv906992	chr16:79649394-79769790	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv833296	chr16:79692236-79889727	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv518748	chr16:79716333-79729031	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79720400-79721600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr16:79720400-79736800	Weak transcription	Aorta	Aorta
3	chr16:79720800-79724200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:79721200-79721600	Enhancers	Duodenum Mucosa	Duodenum
5	chr16:79721200-79721600	Enhancers	K562	blood
6	chr16:79721200-79722400	Enhancers	Osteobl	bone
7	chr16:79721200-79724800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:79721400-79721600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr16:79721400-79721600	Enhancers	Pancreas	Pancrea
10	chr16:79721400-79721800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr16:79721400-79721800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
12	chr16:79721400-79721800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr16:79721400-79722800	Enhancers	NH-A	brain
14	chr16:79721400-79723200	Enhancers	NHDF-Ad	bronchial

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dbSNP/dbVar ID: rs12345 /nsv7879
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