Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10211859	0.99[EUR][1000 genomes]
rs17241270	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2049835	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2049882	0.99[EUR][1000 genomes]
rs2091947	0.90[EUR][1000 genomes]
rs2823234	0.90[EUR][1000 genomes]
rs2823235	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2823236	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2823237	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2823238	0.84[EUR][1000 genomes]
rs2823239	0.84[EUR][1000 genomes]
rs2823242	0.96[EUR][1000 genomes]
rs2823244	0.81[EUR][1000 genomes]
rs6517383	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7278751	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7279326	0.89[EUR][1000 genomes]
rs7280494	0.84[EUR][1000 genomes]
rs7281880	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8128176	0.99[EUR][1000 genomes]
rs9980544	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9981613	0.87[EUR][1000 genomes]
rs9982882	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9982903	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9983155	0.90[EUR][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	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1056659	chr21:16646531-16709391	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1064280	chr21:16664312-17049272	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1812556	chr21:16690063-16736368	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16695200-16697800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr21:16695400-16697600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr21:16695800-16706400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr21:16696000-16696800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr21:16696000-16697000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr21:16696000-16697600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr21:16696200-16698400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr21:16696400-16697600	Enhancers	Liver	Liver

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