Variant report

Variant	nsv1059700
Chromosome Location	chr20:15311358-15323282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:

Extended variants
information (count: 367 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537333830	chr20:15311381-15311382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550838275	chr20:15311387-15311388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569199245	chr20:15311403-15311404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532195531	chr20:15311407-15311408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6079756	chr20:15311431-15311432	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs566634720	chr20:15311471-15311472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542647690	chr20:15311490-15311491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112102290	chr20:15311519-15311520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6079757	chr20:15311550-15311551	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368844440	chr20:15311590-15311591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6079758	chr20:15311604-15311605	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs6043210	chr20:15311611-15311612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574984158	chr20:15311621-15311622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188219082	chr20:15311637-15311638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545178896	chr20:15311638-15311639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564941058	chr20:15311642-15311643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192551680	chr20:15311667-15311668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540311379	chr20:15311682-15311683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10485524	chr20:15311684-15311685	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535179597	chr20:15311691-15311692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73615572	chr20:15311733-15311734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs398088313	chr20:15311734-15311735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2423929	chr20:15311782-15311783	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs184574307	chr20:15311794-15311795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562805523	chr20:15311871-15311872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6131663	chr20:15311873-15311874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs546644413	chr20:15311898-15311899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80194628	chr20:15311912-15311913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112443106	chr20:15311913-15311914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527813873	chr20:15311929-15311930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6074874	chr20:15311938-15311939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs571003216	chr20:15311959-15311960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6079759	chr20:15312001-15312002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs6079760	chr20:15312007-15312008	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs369976328	chr20:15312055-15312056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568748762	chr20:15312077-15312078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553053258	chr20:15312085-15312086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536127136	chr20:15312154-15312155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554635373	chr20:15312196-15312197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373866475	chr20:15312219-15312220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572862736	chr20:15312226-15312227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537315050	chr20:15312229-15312230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375729990	chr20:15312243-15312244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557218062	chr20:15312257-15312258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567647493	chr20:15312346-15312347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533917779	chr20:15312374-15312375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6043211	chr20:15312488-15312489	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs576817318	chr20:15312507-15312508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143112822	chr20:15312540-15312541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553133829	chr20:15312541-15312542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15311000-15311600	Enhancers	Fetal Heart	heart
2	chr20:15311400-15311800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr20:15311800-15312600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr20:15312600-15312800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr20:15312600-15313000	Enhancers	GM12878-XiMat	blood
6	chr20:15312800-15313600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr20:15313000-15313400	Weak transcription	GM12878-XiMat	blood
8	chr20:15313000-15313600	Enhancers	Primary B cells from peripheral blood	blood
9	chr20:15313400-15313600	Active TSS	GM12878-XiMat	blood
10	chr20:15313600-15313800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr20:15313600-15314000	Flanking Active TSS	Primary B cells from peripheral blood	blood
12	chr20:15313600-15315000	Flanking Active TSS	GM12878-XiMat	blood
13	chr20:15314000-15314200	Enhancers	Primary B cells from peripheral blood	blood
14	chr20:15315000-15315400	Active TSS	GM12878-XiMat	blood
15	chr20:15315000-15316000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:15315400-15315600	Enhancers	GM12878-XiMat	blood
17	chr20:15315600-15315800	Flanking Active TSS	GM12878-XiMat	blood
18	chr20:15315800-15316600	Enhancers	GM12878-XiMat	blood
19	chr20:15315800-15317800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr20:15316000-15316800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:15316200-15317200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr20:15316400-15316800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr20:15316400-15316800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr20:15316400-15317400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr20:15316400-15317600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr20:15316400-15317600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr20:15316400-15317800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr20:15316600-15316800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr20:15316600-15317600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr20:15316600-15317600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr20:15316800-15319200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr20:15317000-15317200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:15317200-15317600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr20:15317400-15318400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr20:15318200-15318400	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr20:15318400-15318600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr20:15318400-15319000	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr20:15318600-15318800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr20:15319000-15320400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr20:15319200-15319600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr20:15319400-15320200	Enhancers	Colon Smooth Muscle	Colon
42	chr20:15319600-15320200	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr20:15323200-15324200	Enhancers	Liver	Liver
44	chr20:15323200-15324600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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