Variant report

Variant	nsv883046
Chromosome Location	chr5:151514956-151540888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:151523925..151524850-chr5:151572610..151573431,6	MCF-7	breast:
2	chr5:151522076..151522840-chr5:151650800..151651429,3	MCF-7	breast:
3	chr5:151204677..151205872-chr5:151522532..151523052,3	MCF-7	breast:
4	chr5:151523874..151524765-chr5:151668143..151669088,3	MCF-7	breast:
5	chr5:151204595..151205535-chr5:151522142..151523020,2	K562	blood:
6	chr5:151523879..151524822-chr5:151665463..151666473,3	MCF-7	breast:
7	chr5:151160169..151163153-chr5:151522448..151524598,2	K562	blood:
8	chr5:151523874..151524433-chr5:151668425..151669088,2	MCF-7	breast:
9	chr5:151484112..151485634-chr5:151524575..151526562,2	K562	blood:
10	chr5:151524627..151526976-chr5:151527410..151529295,2	K562	blood:
11	chr5:151303110..151303991-chr5:151522441..151523040,2	MCF-7	breast:
12	chr5:151513919..151516215-chr5:151517657..151519224,2	K562	blood:
13	chr5:151509815..151512281-chr5:151517345..151519719,2	MCF-7	breast:
14	chr5:151523242..151525301-chr5:151526406..151528109,3	MCF-7	breast:
15	chr5:151302299..151302849-chr5:151522311..151522997,2	MCF-7	breast:
16	chr5:151522014..151522696-chr5:151729134..151730175,3	MCF-7	breast:
17	chr5:151524627..151526976-chr5:151527410..151529295,2	K562	blood:
18	chr5:151513919..151516215-chr5:151517657..151519224,2	K562	blood:
19	chr5:151522783..151523283-chr8:54673594..54674407,2	NB4	blood:
20	chr5:151513671..151516215-chr5:151517705..151520059,3	K562	blood:
21	chr5:151523886..151524850-chr5:151572559..151573494,21	MCF-7	breast:
22	chr5:151523912..151524811-chr5:151568652..151569394,2	MCF-7	breast:
23	chr5:151523917..151524489-chr5:151572860..151573489,2	MCF-7	breast:
24	chr5:151513671..151516215-chr5:151517705..151520059,3	K562	blood:
25	chr5:151303407..151303946-chr5:151522386..151523026,2	MCF-7	breast:
26	chr5:151520907..151523004-chr5:151546531..151548901,2	K562	blood:
27	chr5:151204736..151205618-chr5:151521905..151522989,3	MCF-7	breast:
28	chr5:151523242..151525301-chr5:151526406..151528109,3	MCF-7	breast:
29	chr5:151538414..151540360-chr5:151542767..151545602,2	MCF-7	breast:

No data

Extended variants
information (count: 720 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs29824	chr5:151514956-151514957	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546271701	chr5:151514958-151514959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544769960	chr5:151515030-151515031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76695863	chr5:151515031-151515032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112888550	chr5:151515056-151515057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191698817	chr5:151515084-151515085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183993324	chr5:151515099-151515100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559756317	chr5:151515107-151515108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188837998	chr5:151515124-151515125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149936801	chr5:151515199-151515200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112851297	chr5:151515201-151515202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528766749	chr5:151515255-151515256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546906353	chr5:151515260-151515261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565447951	chr5:151515332-151515333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576557492	chr5:151515339-151515340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144105761	chr5:151515350-151515351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191157327	chr5:151515388-151515389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568872129	chr5:151515435-151515436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182206739	chr5:151515440-151515441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148692529	chr5:151515441-151515442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566803664	chr5:151515481-151515482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142745351	chr5:151515504-151515505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558489980	chr5:151515573-151515574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576929194	chr5:151515587-151515588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538760038	chr5:151515610-151515611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557080973	chr5:151515611-151515612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73274933	chr5:151515633-151515634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115276147	chr5:151515677-151515678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560923317	chr5:151515735-151515736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573480027	chr5:151515764-151515765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4958514	chr5:151515891-151515892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565345186	chr5:151515898-151515899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78042906	chr5:151515917-151515918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80139436	chr5:151515918-151515919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532690189	chr5:151515951-151515952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10077195	chr5:151516083-151516084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6871187	chr5:151516086-151516087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529794954	chr5:151516095-151516096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73274935	chr5:151516141-151516142	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs29823	chr5:151516156-151516157	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs566432514	chr5:151516270-151516271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527602483	chr5:151516275-151516276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191634520	chr5:151516284-151516285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184894877	chr5:151516292-151516293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544633436	chr5:151516332-151516333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78069876	chr5:151516358-151516359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555925844	chr5:151516386-151516387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569037165	chr5:151516402-151516403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190187693	chr5:151516410-151516411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554558282	chr5:151516413-151516414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151513800-151515000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:151515000-151518200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:151516000-151516800	Enhancers	Fetal Lung	lung
4	chr5:151516200-151517200	Enhancers	Brain Hippocampus Middle	brain
5	chr5:151516400-151518600	Enhancers	Ovary	ovary
6	chr5:151516600-151516800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:151516600-151516800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
8	chr5:151516600-151518000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:151517600-151518200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:151518200-151518600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr5:151518600-151531200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:151519400-151520400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:151521000-151522400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:151522000-151522800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr5:151522600-151524400	Enhancers	Stomach Mucosa	stomach
16	chr5:151523600-151524800	Enhancers	Placenta	Placenta
17	chr5:151524000-151524800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:151524600-151525200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:151524800-151525800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:151525800-151526000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr5:151526000-151527200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr5:151526600-151527200	Enhancers	Fetal Lung	lung
23	chr5:151526600-151527200	Enhancers	Ovary	ovary
24	chr5:151527200-151527400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:151529200-151529600	Enhancers	Brain Substantia Nigra	brain
26	chr5:151530800-151531600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:151531200-151532000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr5:151532000-151532800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:151532400-151532800	Enhancers	Adipose Nuclei	Adipose
30	chr5:151538800-151540400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr5:151538800-151540600	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr5:151538800-151540800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr5:151538800-151540800	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr5:151538800-151541000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr5:151538800-151541200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:151538800-151541200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr5:151539000-151539400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr5:151539000-151540600	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr5:151539000-151540800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr5:151539200-151539800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:151539200-151540000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr5:151539200-151540200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr5:151539200-151540200	Enhancers	Stomach Mucosa	stomach
44	chr5:151539200-151540800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr5:151539400-151540800	Enhancers	Primary T cells fromperipheralblood	blood
46	chr5:151539600-151539800	Enhancers	Lung	lung
47	chr5:151540400-151541000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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