Variant report

Variant	nsv967441
Chromosome Location	chr7:150566747-150612420
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:74)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:150595297..150595901-chr7:151000224..151001110,2	MCF-7	breast:
2	chr7:150595118..150596336-chr7:150685225..150686536,14	K562	blood:
3	chr7:150588951..150590460-chr7:150591915..150593623,2	K562	blood:
4	chr7:150595285..150595942-chr7:150638602..150639551,2	MCF-7	breast:
5	chr7:150595709..150596608-chr7:150682983..150683767,2	MCF-7	breast:
6	chr7:150484477..150485748-chr7:150573549..150574883,10	MCF-7	breast:
7	chr7:150593671..150595670-chr7:150707603..150709523,2	K562	blood:
8	chr7:150570270..150572638-chr7:150573385..150575681,2	K562	blood:
9	chr7:150588951..150590460-chr7:150591915..150593623,2	K562	blood:
10	chr7:150595230..150595809-chr7:150756656..150757191,2	K562	blood:
11	chr7:150475264..150476504-chr7:150573512..150575222,24	MCF-7	breast:
12	chr7:150570270..150572638-chr7:150573385..150575681,2	K562	blood:
13	chr7:150572726..150575481-chr7:150755589..150757663,2	K562	blood:
14	chr7:150145854..150146458-chr7:150573963..150574703,2	MCF-7	breast:
15	chr7:150477211..150477855-chr7:150573375..150574392,3	K562	blood:
16	chr7:150574063..150575596-chr7:150684914..150687331,2	K562	blood:
17	chr7:150594117..150594813-chr7:150683294..150683813,2	MCF-7	breast:
18	chr7:150588989..150591013-chr7:150594211..150596006,2	K562	blood:
19	chr7:150594719..150596784-chr7:150671045..150673400,2	MCF-7	breast:
20	chr7:150567773..150569879-chr7:150653213..150655593,2	K562	blood:
21	chr7:150595209..150595856-chr7:150691392..150692242,2	K562	blood:
22	chr7:150578874..150579474-chr7:151000674..151001226,2	MCF-7	breast:
23	chr7:150573002..150574576-chr7:150869374..150870431,9	K562	blood:
24	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:
25	chr7:150573795..150574494-chr7:150595524..150596109,2	MCF-7	breast:
26	chr7:150573795..150574494-chr7:150595524..150596109,2	MCF-7	breast:
27	chr7:150575333..150577357-chr7:150717786..150719549,2	K562	blood:
28	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:
29	chr7:150568033..150570583-chr7:150684396..150686354,2	MCF-7	breast:
30	chr7:150595318..150596192-chr7:150714946..150715892,2	MCF-7	breast:
31	chr7:150589872..150593985-chr7:150595485..150599567,4	K562	blood:
32	chr7:150596864..150597764-chr7:150685476..150685984,2	MCF-7	breast:
33	chr7:150562856..150565769-chr7:150566346..150570295,3	K562	blood:
34	chr7:150595860..150599286-chr7:150714310..150716664,3	K562	blood:
35	chr7:150588989..150591013-chr7:150594211..150596006,2	K562	blood:
36	chr7:150595255..150596427-chr7:150685626..150686266,3	MCF-7	breast:
37	chr7:150612304..150615151-chr7:150617269..150619217,3	K562	blood:
38	chr7:150595154..150595801-chr7:150808802..150809459,2	K562	blood:
39	chr7:150475409..150476275-chr7:150572596..150573318,2	MCF-7	breast:
40	chr7:150595261..150596228-chr7:150705729..150706424,2	K562	blood:
41	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:
42	chr7:150595334..150596475-chr7:150715020..150715911,4	K562	blood:
43	chr7:150607061..150610387-chr7:150610686..150614905,4	K562	blood:
44	chr7:150592534..150594074-chr7:150674955..150677260,2	MCF-7	breast:
45	chr7:150145511..150146032-chr7:150573896..150574858,2	K562	blood:
46	chr7:150485004..150485681-chr7:150573803..150574496,3	MCF-7	breast:
47	chr7:150597420..150599552-chr7:150675376..150678121,2	K562	blood:
48	chr7:150607061..150610387-chr7:150610686..150614905,4	K562	blood:
49	chr7:150593930..150595766-chr7:150657533..150659596,2	K562	blood:
50	chr7:150595224..150596309-chr7:150682667..150684079,9	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABP1-1	chr7:150568035-150568307	expRegAs_chr7_12357_+
2	lnc-ABP1-2	chr7:150568389-150569059	predAs_engstrom06_BM715580_1

No data

Variant related genes	Relation type
ENSG00000181652	chromatin interactions
ENSG00000164867	chromatin interactions
ENSG00000164889	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000055118	chromatin interactions

Extended variants
information (count: 1337 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142879541	chr7:150566772-150566773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540079075	chr7:150566855-150566856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112650560	chr7:150566857-150566858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151052497	chr7:150566887-150566888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532159796	chr7:150566891-150566892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566703741	chr7:150566949-150566950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551872307	chr7:150566955-150566956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530916457	chr7:150567003-150567004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140299490	chr7:150567012-150567013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564341442	chr7:150567013-150567014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550972243	chr7:150567032-150567033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528432121	chr7:150567077-150567078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568006125	chr7:150567079-150567080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547317923	chr7:150567088-150567089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536934433	chr7:150567095-150567096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547273318	chr7:150567136-150567137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs67091546	chr7:150567184-150567185	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538823927	chr7:150567193-150567194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558653726	chr7:150567204-150567205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183928384	chr7:150567216-150567217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537496919	chr7:150567224-150567225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188359269	chr7:150567253-150567254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181185899	chr7:150567268-150567269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377020268	chr7:150567277-150567278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73165560	chr7:150567295-150567296	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs186555662	chr7:150567312-150567313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560157300	chr7:150567325-150567326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146996941	chr7:150567333-150567334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545661602	chr7:150567342-150567343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138108403	chr7:150567433-150567434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114742830	chr7:150567502-150567503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548094544	chr7:150567503-150567504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551033786	chr7:150567523-150567524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73165561	chr7:150567561-150567562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs111645229	chr7:150567565-150567566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73468631	chr7:150567570-150567571	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560291606	chr7:150567651-150567652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369128552	chr7:150567674-150567675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539250372	chr7:150567711-150567712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552494885	chr7:150567727-150567728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4266560	chr7:150567741-150567742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs537558858	chr7:150567892-150567893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73165562	chr7:150567934-150567935	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574114576	chr7:150567949-150567950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533508599	chr7:150567991-150567992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554066103	chr7:150568028-150568029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73468632	chr7:150568069-150568070	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142308816	chr7:150568084-150568085	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs146115989	chr7:150568090-150568091	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs113344058	chr7:150568125-150568126	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150563000-150573800	Weak transcription	Fetal Stomach	stomach
2	chr7:150564200-150573800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:150565000-150573000	Weak transcription	Ovary	ovary
4	chr7:150565800-150567400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:150565800-150567600	Enhancers	Liver	Liver
6	chr7:150567400-150573000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:150568800-150569000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:150569000-150576600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:150572000-150572200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:150572000-150574400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr7:150572200-150573800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:150572400-150574400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:150572400-150574600	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr7:150572600-150574200	Weak transcription	Colon Smooth Muscle	Colon
15	chr7:150572600-150574400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr7:150572600-150574800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr7:150572800-150574000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr7:150572800-150574400	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr7:150572800-150574400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:150573000-150573200	Enhancers	Brain Hippocampus Middle	brain
21	chr7:150573000-150573600	Enhancers	Ovary	ovary
22	chr7:150573000-150573800	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr7:150573000-150574000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
24	chr7:150573000-150574400	Enhancers	Primary T cells fromperipheralblood	blood
25	chr7:150573000-150574400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr7:150573000-150574600	Enhancers	Primary B cells from peripheral blood	blood
27	chr7:150573000-150575800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:150573200-150574000	Enhancers	Primary T cells from cord blood	blood
29	chr7:150573200-150574000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:150573200-150574200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:150573200-150574600	Enhancers	Liver	Liver
32	chr7:150573200-150574600	Enhancers	Brain Cingulate Gyrus	brain
33	chr7:150573400-150573800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:150573400-150574000	Weak transcription	Brain Hippocampus Middle	brain
35	chr7:150573600-150573800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr7:150573600-150573800	Weak transcription	Ovary	ovary
37	chr7:150573600-150574000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:150573600-150574000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:150573600-150574000	Enhancers	Duodenum Mucosa	Duodenum
40	chr7:150573600-150574200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr7:150573600-150574800	Enhancers	Brain Anterior Caudate	brain
42	chr7:150573800-150574000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:150573800-150574000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:150573800-150574000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:150573800-150574000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr7:150573800-150574000	Bivalent/Poised TSS	K562	blood
47	chr7:150573800-150574200	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr7:150573800-150574200	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr7:150573800-150574200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr7:150573800-150574200	Active TSS	Colonic Mucosa	Colon

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