Variant report

Variant	rs62208582
Chromosome Location	chr21:15465061-15465062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10854277	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10854278	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10854279	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11087909	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11087910	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12151976	0.82[EUR][1000 genomes]
rs12483211	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12483328	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12483373	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1974407	0.82[EUR][1000 genomes]
rs2187275	0.81[EUR][1000 genomes]
rs2187276	0.81[EUR][1000 genomes]
rs2226731	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2822399	0.86[EUR][1000 genomes]
rs2822400	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2822401	0.83[EUR][1000 genomes]
rs2822402	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2822403	0.83[EUR][1000 genomes]
rs2822405	0.81[EUR][1000 genomes]
rs28575716	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35777238	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4816224	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4816225	0.81[AFR][1000 genomes]
rs4816941	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4816942	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4816945	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55774504	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55930907	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56809490	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56964975	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs57368517	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs58106611	0.83[EUR][1000 genomes]
rs58814444	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59363534	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60578285	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs60702377	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60707485	0.82[AMR][1000 genomes]
rs62208560	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62208573	0.83[EUR][1000 genomes]
rs62208574	0.83[EUR][1000 genomes]
rs62208575	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62208581	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62208583	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62208584	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62208585	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62208586	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62208587	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62208588	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62208589	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62211266	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62211267	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6516610	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7275860	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7275968	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7276133	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7276424	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7276925	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7277769	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7277845	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7280792	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7281456	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7281918	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7282128	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73342118	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73342122	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8126892	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8131499	0.83[EUR][1000 genomes]
rs8131762	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8132276	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8133014	0.81[EUR][1000 genomes]
rs8133096	0.81[EUR][1000 genomes]
rs9789852	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9789885	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9976316	0.81[EUR][1000 genomes]
rs9984737	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058202	chr21:14706767-15628668	Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	nsv1067433	chr21:14736298-15507502	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1055396	chr21:14756514-15507502	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv1062639	chr21:14775729-15507502	Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
5	nsv1058072	chr21:15372509-15568171	Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1056787	chr21:15407504-15530291	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1831533	chr21:15442382-15477876	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	n/a
8	esv1827667	chr21:15442582-15521121	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv1827538	chr21:15446711-15472381	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	inside rSNPs	n/a
10	esv990249	chr21:15446864-15471276	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
11	esv1830377	chr21:15446911-15477676	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	inside rSNPs	n/a
12	esv1830288	chr21:15448891-15474325	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	n/a
13	esv32571	chr21:15456265-15467954	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15441000-15470200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr21:15444200-15475400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr21:15455800-15479800	Weak transcription	Colon Smooth Muscle	Colon
4	chr21:15456000-15470000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr21:15456800-15470200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr21:15457000-15467600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr21:15457400-15465200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr21:15457600-15465200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr21:15457600-15465200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr21:15457600-15465200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr21:15457600-15465400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr21:15457600-15465400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr21:15457600-15465800	Weak transcription	Hela-S3	cervix
14	chr21:15457600-15470000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr21:15457600-15470200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr21:15457600-15470200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr21:15457600-15470200	Weak transcription	Adipose Nuclei	Adipose
18	chr21:15457600-15470200	Weak transcription	Esophagus	oesophagus
19	chr21:15457600-15472800	Weak transcription	Fetal Muscle Leg	muscle
20	chr21:15457600-15473800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr21:15457600-15487400	Weak transcription	Fetal Brain Male	brain
22	chr21:15457800-15467800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr21:15457800-15486200	Weak transcription	Thymus	Thymus
24	chr21:15458000-15465400	Weak transcription	Fetal Stomach	stomach
25	chr21:15458000-15466000	Weak transcription	Fetal Intestine Small	intestine
26	chr21:15459200-15466000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr21:15459600-15469000	Weak transcription	Brain Germinal Matrix	brain
28	chr21:15459800-15470200	Weak transcription	Ovary	ovary
29	chr21:15460000-15470200	Weak transcription	Fetal Lung	lung
30	chr21:15460200-15467400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr21:15461000-15470200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr21:15462200-15465800	Strong transcription	Dnd41	blood
33	chr21:15462400-15471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr21:15463000-15465800	ZNF genes & repeats	GM12878-XiMat	blood
35	chr21:15463200-15470200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr21:15463200-15472200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr21:15463400-15470200	Weak transcription	Gastric	stomach
38	chr21:15463800-15465800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr21:15464200-15468000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr21:15464400-15470200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr21:15464600-15466000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr21:15464600-15467400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr21:15464600-15469800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr21:15464600-15470000	Weak transcription	Fetal Brain Female	brain
45	chr21:15464600-15470200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr21:15464800-15465400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr21:15464800-15466200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr21:15464800-15466200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr21:15464800-15470200	Weak transcription	K562	blood

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