Variant report

Variant	nsv605936
Chromosome Location	chr7:3722433-3766819
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
2	chr7:3757251..3758935-chr7:3765168..3767703,2	MCF-7	breast:
3	chr7:3757251..3758935-chr7:3765168..3767703,2	MCF-7	breast:
4	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
5	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
6	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:
7	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
8	chr7:3734945..3735889-chr7:3936899..3937757,3	MCF-7	breast:
9	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
10	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
11	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:

No data

Extended variants
information (count: 2607 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2607 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6462225	chr7:3722433-3722434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532332420	chr7:3722439-3722440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185045615	chr7:3722445-3722446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376080808	chr7:3722449-3722450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577230496	chr7:3722456-3722457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534663166	chr7:3722509-3722510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370470709	chr7:3722518-3722519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190332983	chr7:3722522-3722523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567829284	chr7:3722526-3722527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6462226	chr7:3722544-3722545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs556516807	chr7:3722555-3722556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576654421	chr7:3722568-3722569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76157387	chr7:3722592-3722593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545426494	chr7:3722595-3722596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558902829	chr7:3722615-3722616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572118194	chr7:3722632-3722633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181112644	chr7:3722636-3722637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140296029	chr7:3722661-3722662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115743654	chr7:3722662-3722663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371187904	chr7:3722665-3722666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144523243	chr7:3722688-3722689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563381257	chr7:3722695-3722696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147840314	chr7:3722725-3722726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186591036	chr7:3722760-3722761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565630367	chr7:3722780-3722781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6462227	chr7:3722799-3722800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs148881657	chr7:3722801-3722802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568149451	chr7:3722810-3722811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188242308	chr7:3722841-3722842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556715594	chr7:3722853-3722854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570195796	chr7:3722860-3722861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181057621	chr7:3722863-3722864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1864841	chr7:3722879-3722880	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374672023	chr7:3722897-3722898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572079935	chr7:3722962-3722963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186357754	chr7:3723004-3723005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141069137	chr7:3723048-3723049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554570578	chr7:3723133-3723134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386709488	chr7:3723154-3723155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1864840	chr7:3723155-3723156	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs563455423	chr7:3723157-3723158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576965622	chr7:3723161-3723162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374373561	chr7:3723162-3723163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74799254	chr7:3723214-3723215	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs559698309	chr7:3723226-3723227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs113412779	chr7:3723227-3723228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs548188970	chr7:3723230-3723231	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs150977540	chr7:3723231-3723232	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs530621963	chr7:3723237-3723238	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs184108314	chr7:3723249-3723250	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3688800-3728400	Weak transcription	Aorta	Aorta
2	chr7:3704000-3723600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:3708600-3723600	Weak transcription	Stomach Mucosa	stomach
4	chr7:3711800-3723600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:3721200-3723400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:3721600-3723200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:3721800-3724200	Enhancers	Fetal Intestine Small	intestine
8	chr7:3721800-3724400	Enhancers	Fetal Intestine Large	intestine
9	chr7:3722200-3723000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr7:3722200-3723200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr7:3722200-3723200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:3722200-3723200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr7:3722200-3723400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:3722200-3723600	Weak transcription	Gastric	stomach
15	chr7:3722200-3723600	Weak transcription	Spleen	Spleen
16	chr7:3722200-3738000	Weak transcription	Pancreas	Pancrea
17	chr7:3722400-3723200	Enhancers	HepG2	liver
18	chr7:3722400-3725400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr7:3722800-3724400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:3722800-3724400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr7:3723000-3724200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:3723000-3728600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:3723200-3723400	Enhancers	Fetal Kidney	kidney
24	chr7:3723200-3724000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:3723200-3724000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:3723200-3724000	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr7:3723200-3724000	Flanking Active TSS	HepG2	liver
28	chr7:3723200-3724200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:3723200-3724200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr7:3723200-3724200	Enhancers	Duodenum Mucosa	Duodenum
31	chr7:3723200-3724200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr7:3723200-3724400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:3723200-3724600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:3723200-3724600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:3723200-3724800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:3723400-3724200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr7:3723400-3724200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr7:3723600-3723800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:3723600-3723800	ZNF genes & repeats	Gastric	stomach
40	chr7:3723600-3723800	ZNF genes & repeats	Spleen	Spleen
41	chr7:3723600-3724000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:3723600-3724000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:3723600-3724200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:3723600-3724200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:3723800-3724000	Enhancers	Esophagus	oesophagus
46	chr7:3723800-3724000	Enhancers	Stomach Mucosa	stomach
47	chr7:3723800-3724400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr7:3724000-3724200	Enhancers	Fetal Kidney	kidney
49	chr7:3724000-3724400	Enhancers	HepG2	liver
50	chr7:3724000-3728400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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