Variant report

Variant	nsv538702
Chromosome Location	chr7:4488856-4559028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
4	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
5	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
6	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
7	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
8	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
9	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
10	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
12	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
13	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
14	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
15	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
16	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
17	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
18	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
19	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
20	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
21	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
22	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
23	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
24	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
25	CHD1	chr7:4541262-4541349	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr7:4519143-4519145	GM12878	blood:	n/a	n/a
27	CHD2	chr7:4540385-4540761	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:4519069-4519290	IMR90	lung:	n/a	n/a
29	CTCF	chr7:4519088-4519321	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr7:4519064-4519397	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr7:4519140-4519290	GM12867	blood:	n/a	n/a
32	CTCF	chr7:4519200-4519350	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr7:4519120-4519270	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr7:4519280-4519430	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr7:4512560-4512710	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr7:4519100-4519250	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr7:4519044-4519372	T-47D	breast:	n/a	n/a
38	CTCF	chr7:4519180-4519330	AG09309	skin:	n/a	n/a
39	CTCF	chr7:4519120-4519270	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr7:4542940-4543090	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:4512513-4512681	A549	lung:	n/a	n/a
42	CTCF	chr7:4490260-4490410	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:4519103-4519346	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:4519149-4519258	GM13977	blood:	n/a	n/a
45	CTCF	chr7:4512581-4512621	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr7:4519220-4519370	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr7:4519140-4519290	HCT-116	colon:	n/a	n/a
48	CTCF	chr7:4512479-4512710	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:4543000-4543150	HepG2	liver:	n/a	n/a
50	CTCF	chr7:4512502-4512628	SK-N-SH_RA	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4536864-4536914	MCF10A-Er-Src	breast:	n/a
2	chr7:4536864-4536914	GM06990	blood:	n/a
3	chr7:4536864-4536914	AG09319	gingival:	n/a
4	chr7:4536864-4536914	SK-N-MC	brain:	n/a
5	chr7:4536838-4536888	SKMC	muscle:	n/a
6	chr7:4536864-4536914	Hela-S3	cervix:	n/a
7	chr7:4536864-4536914	H1-hESC	embryonic stem cell:	embryo
8	chr7:4536864-4536914	HEEpiC	esophagus:	n/a
9	chr7:4536838-4536888	NH-A	brain:	n/a
10	chr7:4536838-4536888	HL-60	blood:	n/a
11	chr7:4536864-4536914	K562	blood:	n/a
12	chr7:4536838-4536888	HRPEpiC	eye:	n/a
13	chr7:4536838-4536888	SK-N-SH_RA	brain:	n/a
14	chr7:4536864-4536914	A549	lung:	n/a
15	chr7:4536838-4536888	LNCaP	prostate:	n/a
16	chr7:4536838-4536888	PANC-1	pancreas:	n/a
17	chr7:4536838-4536888	AG09309	skin:	n/a
18	chr7:4536838-4536888	NHDF-neo	bronchial:	n/a
19	chr7:4536838-4536888	PrEC	prostate:	n/a
20	chr7:4536864-4536914	IMR90	lung:	fetal
21	chr7:4536864-4536914	BJ	skin:	n/a
22	chr7:4536838-4536888	ProgFib	skin:	n/a
23	chr7:4536864-4536914	PrEC	prostate:	n/a
24	chr7:4536838-4536888	AoSMC	blood vessel:	n/a
25	chr7:4536838-4536888	Hela-S3	cervix:	n/a
26	chr7:4536864-4536914	NT2-D1	testis:	n/a
27	chr7:4536838-4536888	HCM	heart:	n/a
28	chr7:4536838-4536888	HIPEpiC	eye:	n/a
29	chr7:4536838-4536888	HepG2	liver:	n/a
30	chr7:4536864-4536914	AG04450	lung:	fetal
31	chr7:4536838-4536888	GM06990	blood:	n/a
32	chr7:4536838-4536888	K562	blood:	n/a
33	chr7:4536838-4536888	AG09319	gingival:	n/a
34	chr7:4536864-4536914	HEK293	kidney:	embryo
35	chr7:4536864-4536914	AG09309	skin:	n/a
36	chr7:4536864-4536914	SAEC	small airway:	n/a
37	chr7:4536864-4536914	CMK	blood:	n/a
38	chr7:4536838-4536888	AG04449	skin:	fetal
39	chr7:4536864-4536914	SKMC	muscle:	n/a
40	chr7:4536838-4536888	T-47D	breast:	n/a
41	chr7:4536864-4536914	HL-60	blood:	n/a
42	chr7:4536838-4536888	HCF	heart:	n/a
43	chr7:4536838-4536888	NT2-D1	testis:	n/a
44	chr7:4536864-4536914	ECC-1	luminal epithelium:	n/a
45	chr7:4536864-4536914	ProgFib	skin:	n/a
46	chr7:4536864-4536914	GM12891	blood:	n/a
47	chr7:4536864-4536914	AG04449	skin:	fetal
48	chr7:4536864-4536914	HIPEpiC	eye:	n/a
49	chr7:4536864-4536914	HCPEpiC	choroid plexus:	n/a
50	chr7:4536838-4536888	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
2	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
3	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
4	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
5	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
6	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
7	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
8	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
9	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
10	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
11	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
2	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
3	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863

No data

Variant related genes	Relation type
CYP3A54P	TF binding region
CYP3A54P	CpG island
ENSG00000261809	chromatin interactions
VEGFA	miRNA target sites

Extended variants
information (count: 1272 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530987518	chr7:4488869-4488870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146312663	chr7:4488870-4488871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570864480	chr7:4488875-4488876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533362923	chr7:4488883-4488884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575125499	chr7:4488948-4488949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546944404	chr7:4488975-4488976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566758520	chr7:4488985-4488986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73671702	chr7:4488994-4488995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555513539	chr7:4489005-4489006	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567598512	chr7:4489045-4489046	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528476652	chr7:4489065-4489066	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375434878	chr7:4489078-4489079	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376593241	chr7:4489085-4489086	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537907374	chr7:4489090-4489091	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375673304	chr7:4489097-4489098	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7811954	chr7:4489132-4489133	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79304004	chr7:4489140-4489141	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144557399	chr7:4489156-4489157	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573169702	chr7:4489172-4489173	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542061003	chr7:4489196-4489197	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562267295	chr7:4489203-4489204	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11981362	chr7:4489207-4489208	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575560466	chr7:4489208-4489209	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79826496	chr7:4489214-4489215	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113689967	chr7:4489222-4489223	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149828998	chr7:4489241-4489242	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145797638	chr7:4489255-4489256	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371139018	chr7:4489261-4489262	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566797568	chr7:4489262-4489263	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539254369	chr7:4489272-4489273	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557552655	chr7:4489273-4489274	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141254832	chr7:4489329-4489330	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568981492	chr7:4489370-4489371	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375622330	chr7:4489443-4489444	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569076484	chr7:4489458-4489459	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537620101	chr7:4489467-4489468	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535886475	chr7:4489489-4489490	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145113370	chr7:4489524-4489525	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545898716	chr7:4489536-4489537	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79546167	chr7:4489548-4489549	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553305040	chr7:4489551-4489552	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369438498	chr7:4489565-4489566	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554642444	chr7:4489591-4489592	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573210392	chr7:4489608-4489609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542549564	chr7:4489628-4489629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555780453	chr7:4489652-4489653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187159368	chr7:4489664-4489665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544465614	chr7:4489689-4489690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117852312	chr7:4489692-4489693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557092262	chr7:4489711-4489712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4485800-4491400	Weak transcription	Fetal Kidney	kidney
2	chr7:4488600-4489400	Enhancers	HepG2	liver
3	chr7:4488600-4489600	Enhancers	Fetal Intestine Large	intestine
4	chr7:4488600-4489600	Enhancers	Fetal Intestine Small	intestine
5	chr7:4489000-4489600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:4497200-4498000	Enhancers	Fetal Muscle Trunk	muscle
7	chr7:4497400-4498200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr7:4497400-4498200	Enhancers	Adipose Nuclei	Adipose
9	chr7:4497400-4498600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:4497400-4498600	Enhancers	Fetal Muscle Leg	muscle
11	chr7:4497400-4498600	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr7:4497400-4498800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:4497400-4498800	Enhancers	Ovary	ovary
14	chr7:4497600-4498200	Enhancers	Brain Germinal Matrix	brain
15	chr7:4497600-4498200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr7:4497600-4498400	Enhancers	Colon Smooth Muscle	Colon
17	chr7:4497600-4498400	Enhancers	Fetal Brain Male	brain
18	chr7:4497600-4498600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:4497800-4498200	Enhancers	Fetal Brain Female	brain
20	chr7:4498000-4498600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
21	chr7:4498200-4498600	Enhancers	Brain Hippocampus Middle	brain
22	chr7:4498600-4500200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr7:4498600-4500200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:4499600-4499800	Enhancers	Aorta	Aorta
25	chr7:4499800-4500600	Enhancers	Fetal Intestine Large	intestine
26	chr7:4499800-4502600	Weak transcription	Aorta	Aorta
27	chr7:4500200-4500600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:4500200-4500600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:4500200-4501200	Enhancers	Fetal Intestine Small	intestine
30	chr7:4500200-4502600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr7:4500800-4501400	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr7:4501400-4501600	Active TSS	Monocytes-CD14+_RO01746	blood
33	chr7:4501600-4501800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr7:4509000-4510000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr7:4509000-4510000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:4509200-4509600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:4509200-4509800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr7:4509400-4509800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:4509400-4510000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:4509600-4510000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:4509600-4510000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr7:4509600-4510200	Enhancers	Aorta	Aorta
43	chr7:4509800-4513200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:4510000-4511200	Enhancers	Brain Germinal Matrix	brain
45	chr7:4510000-4512200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr7:4510000-4512200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:4510000-4512400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr7:4512200-4512400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:4512200-4513000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:4512200-4513000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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