Variant report

Variant	rs13046821
Chromosome Location	chr21:16597060-16597061
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11909130	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12482026	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12483396	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12483484	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13051325	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13052858	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2064040	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2823148	0.89[EUR][1000 genomes]
rs2823149	0.90[EUR][1000 genomes]
rs2823151	0.90[EUR][1000 genomes]
rs2823154	0.89[EUR][1000 genomes]
rs2823155	0.88[EUR][1000 genomes]
rs2823160	0.99[ASN][1000 genomes]
rs2823163	0.99[ASN][1000 genomes]
rs2823165	0.99[ASN][1000 genomes]
rs2823166	0.88[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2823167	0.88[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2823168	0.88[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2823169	0.98[ASN][1000 genomes]
rs2823172	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2823173	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2823174	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823176	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823178	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2823179	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2823180	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2823181	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6517301	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6517302	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6517303	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7281303	0.88[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs8131982	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9808777	0.89[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	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	nsv913413	chr21:16537728-16621859	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv587059	chr21:16588414-16600408	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16591600-16597400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr21:16592200-16597800	Enhancers	Hela-S3	cervix
3	chr21:16592400-16597800	Enhancers	NHEK	skin
4	chr21:16592800-16597400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr21:16593000-16597600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr21:16593400-16597400	Enhancers	NHLF	lung
7	chr21:16593600-16597800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr21:16593800-16597200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr21:16593800-16598000	Enhancers	HMEC	breast
10	chr21:16594000-16597400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr21:16594200-16597400	Enhancers	Osteobl	bone
12	chr21:16594400-16597400	Enhancers	NHDF-Ad	bronchial
13	chr21:16594400-16597800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr21:16594600-16597200	Weak transcription	Esophagus	oesophagus
15	chr21:16595800-16597400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr21:16596400-16597400	Enhancers	NH-A	brain
17	chr21:16596600-16597200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr21:16596600-16597400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr21:16596800-16597400	Active TSS	A549	lung
20	chr21:16597000-16597200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr21:16597000-16597200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr21:16597000-16597400	Enhancers	HSMM	muscle

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