Variant report

Variant	rs16993384
Chromosome Location	chr21:17445961-17445962
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16993387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16993393	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16993394	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16993505	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs16993558	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs16993988	1.00[MEX][hapmap]
rs57469115	1.00[AMR][1000 genomes]
rs57936518	1.00[AMR][1000 genomes]
rs58529486	1.00[AMR][1000 genomes]
rs59631437	1.00[AMR][1000 genomes]
rs60167288	1.00[AMR][1000 genomes]
rs60300181	1.00[AMR][1000 genomes]
rs881073	1.00[AMR][1000 genomes]
rs881074	1.00[AMR][1000 genomes]
rs881076	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913414	chr21:17383785-17459507	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv913415	chr21:17400916-17452276	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2830060	chr21:17400916-17459507	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv527854	chr21:17400916-17459507	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv1851038	chr21:17412144-17488119	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17441600-17446800	Active TSS	Fetal Brain Female	brain
2	chr21:17442000-17446200	Active TSS	Brain Angular Gyrus	brain
3	chr21:17442000-17446400	Active TSS	Brain Cingulate Gyrus	brain
4	chr21:17442000-17446800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr21:17442000-17447200	Active TSS	Fetal Brain Male	brain
6	chr21:17442000-17448000	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr21:17442400-17446200	Active TSS	Brain Anterior Caudate	brain
8	chr21:17442400-17446200	Active TSS	Brain Substantia Nigra	brain
9	chr21:17443000-17448200	Active TSS	Brain Hippocampus Middle	brain
10	chr21:17444000-17446200	Flanking Active TSS	NH-A	brain
11	chr21:17444600-17446400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr21:17445200-17446200	Enhancers	Fetal Kidney	kidney
13	chr21:17445200-17457200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr21:17445400-17446000	Active TSS	Brain Germinal Matrix	brain
15	chr21:17445400-17446000	Flanking Active TSS	NHDF-Ad	bronchial
16	chr21:17445600-17446200	Enhancers	Osteobl	bone
17	chr21:17445800-17446200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr21:17445800-17446200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr21:17445800-17446200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr21:17445800-17446400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr21:17445800-17446600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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