Variant report

Variant	rs7277187
Chromosome Location	chr21:17584461-17584462
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11088577	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1492952	0.88[CEU][hapmap]
rs1492953	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1619989	0.83[AMR][1000 genomes]
rs190229	0.84[AMR][1000 genomes]
rs2156360	0.93[AMR][1000 genomes]
rs239003	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs239006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2639700	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823638	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823639	0.87[CEU][hapmap]
rs2823641	0.89[CEU][hapmap]
rs2823642	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823643	0.89[CEU][hapmap]
rs2823646	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs2823650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823651	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823652	0.87[CEU][hapmap]
rs2823653	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823657	0.87[CEU][hapmap]
rs2823658	0.88[CEU][hapmap]
rs2823659	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2823660	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2823661	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2823662	1.00[JPT][hapmap]
rs35934547	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6650848	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6650849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7276974	1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7283145	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs915799	0.92[CEU][hapmap]
rs9637000	0.88[CEU][hapmap]
rs983530	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9974416	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9983241	0.92[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	nsv1066951	chr21:17458978-17603160	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv544381	chr21:17458978-17603160	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv432145	chr21:17559229-17628529	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv834051	chr21:17564843-17721764	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17576000-17596800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr21:17582200-17585400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr21:17583000-17585000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr21:17583600-17584600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr21:17583600-17584600	Enhancers	Fetal Kidney	kidney
6	chr21:17583600-17584600	Enhancers	Right Atrium	heart
7	chr21:17583600-17584800	Enhancers	Brain Angular Gyrus	brain
8	chr21:17583600-17585400	Enhancers	Brain Cingulate Gyrus	brain
9	chr21:17583600-17586200	Enhancers	Brain Hippocampus Middle	brain
10	chr21:17583800-17584600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr21:17583800-17584600	Flanking Active TSS	Brain Anterior Caudate	brain
12	chr21:17583800-17584600	Enhancers	HUVEC	blood vessel
13	chr21:17583800-17585200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr21:17583800-17585400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr21:17584000-17584600	Enhancers	Primary hematopoietic stem cells	blood
16	chr21:17584000-17584600	Enhancers	Aorta	Aorta
17	chr21:17584000-17584600	Enhancers	Fetal Lung	lung
18	chr21:17584000-17584800	Flanking Active TSS	Osteobl	bone
19	chr21:17584000-17585000	Flanking Active TSS	Fetal Heart	heart
20	chr21:17584000-17585000	Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr21:17584000-17585400	Active TSS	Psoas Muscle	Psoas
22	chr21:17584000-17587600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr21:17584000-17598800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr21:17584200-17584600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr21:17584200-17584600	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr21:17584200-17584600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr21:17584200-17584800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr21:17584200-17585000	Active TSS	NHDF-Ad	bronchial
29	chr21:17584200-17585200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr21:17584200-17585600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr21:17584200-17586200	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr21:17584200-17587800	Weak transcription	Brain Substantia Nigra	brain
33	chr21:17584200-17592200	Weak transcription	Fetal Muscle Leg	muscle
34	chr21:17584200-17592200	Weak transcription	Fetal Stomach	stomach
35	chr21:17584400-17584600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr21:17584400-17584600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr21:17584400-17584600	Flanking Active TSS	HSMMtube	muscle
38	chr21:17584400-17584800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr21:17584400-17584800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr21:17584400-17585000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr21:17584400-17585400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr21:17584400-17586800	Enhancers	Liver	Liver
43	chr21:17584400-17588200	Weak transcription	Colon Smooth Muscle	Colon
44	chr21:17584400-17596800	Weak transcription	Ovary	ovary
45	chr21:17584400-17619400	Weak transcription	Hela-S3	cervix

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