Variant report

Variant	esv2752157
Chromosome Location	chr7:4477992-4645389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:305)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4601500-4601710	K562	blood:	n/a	n/a
2	ARID3A	chr7:4573177-4573308	K562	blood:	n/a	n/a
3	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
5	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
6	CBX3	chr7:4592673-4592898	K562	blood:	n/a	n/a
7	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
8	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
9	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
10	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
11	CEBPB	chr7:4606462-4606612	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:4606356-4606720	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:4606437-4606623	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
15	CEBPB	chr7:4606920-4607086	HepG2	liver:	n/a	chr7:4606937-4606948
16	CEBPB	chr7:4606355-4606641	K562	blood:	n/a	n/a
17	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
18	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
19	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
20	CEBPB	chr7:4606348-4606704	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
22	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
23	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
24	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
25	CEBPB	chr7:4606335-4606705	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
27	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
29	CEBPB	chr7:4606357-4606697	A549	lung:	n/a	n/a
30	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
31	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
32	CEBPB	chr7:4606365-4606717	A549	lung:	n/a	n/a
33	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
34	CEBPB	chr7:4584957-4585000	HepG2	liver:	n/a	chr7:4584972-4584983
35	CEBPB	chr7:4606363-4606718	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:4606342-4606723	K562	blood:	n/a	n/a
37	CEBPB	chr7:4606331-4606697	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr7:4562189-4562372	K562	blood:	n/a	chr7:4562300-4562311
39	CEBPB	chr7:4585045-4585090	A549	lung:	n/a	n/a
40	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
41	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
42	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
43	CEBPB	chr7:4606356-4606718	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:4606368-4606733	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
46	CEBPB	chr7:4606287-4606701	A549	lung:	n/a	n/a
47	CEBPD	chr7:4573063-4573272	K562	blood:	n/a	n/a
48	CEBPD	chr7:4478262-4478862	K562	blood:	n/a	n/a
49	CEBPD	chr7:4478238-4478981	K562	blood:	n/a	n/a
50	CEBPD	chr7:4572950-4573325	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4630518-4630568	H1-hESC	embryonic stem cell:	embryo
2	chr7:4573716-4573766	PANC-1	pancreas:	n/a
3	chr7:4573535-4573585	SK-N-MC	brain:	n/a
4	chr7:4573716-4573766	SK-N-MC	brain:	n/a
5	chr7:4573716-4573766	SK-N-SH_RA	brain:	n/a
6	chr7:4573535-4573585	HCM	heart:	n/a
7	chr7:4536864-4536914	SK-N-SH	brain:	n/a
8	chr7:4573716-4573766	AG04449	skin:	fetal
9	chr7:4573535-4573585	AG10803	skin:	n/a
10	chr7:4573535-4573585	AoSMC	blood vessel:	n/a
11	chr7:4536838-4536888	HMEC	breast:	n/a
12	chr7:4573716-4573766	NHDF-neo	bronchial:	n/a
13	chr7:4536838-4536888	Hela-S3	cervix:	n/a
14	chr7:4630518-4630568	Caco-2	colon:	n/a
15	chr7:4573716-4573766	HRCEpiC	kidney:	n/a
16	chr7:4630518-4630568	AG09309	skin:	n/a
17	chr7:4630518-4630568	CMK	blood:	n/a
18	chr7:4573716-4573766	HCF	heart:	n/a
19	chr7:4573535-4573585	HCPEpiC	choroid plexus:	n/a
20	chr7:4536838-4536888	MCF10A-Er-Src	breast:	n/a
21	chr7:4573535-4573585	ECC-1	luminal epithelium:	n/a
22	chr7:4536864-4536914	GM19239	blood:	n/a
23	chr7:4536838-4536888	AoSMC	blood vessel:	n/a
24	chr7:4536838-4536888	U87	brain:	n/a
25	chr7:4573716-4573766	HEEpiC	esophagus:	n/a
26	chr7:4573535-4573585	HIPEpiC	eye:	n/a
27	chr7:4536838-4536888	CMK	blood:	n/a
28	chr7:4536838-4536888	ProgFib	skin:	n/a
29	chr7:4573716-4573766	HCT-116	colon:	n/a
30	chr7:4573716-4573766	HepG2	liver:	n/a
31	chr7:4630518-4630568	NT2-D1	testis:	n/a
32	chr7:4536864-4536914	HRCEpiC	kidney:	n/a
33	chr7:4573535-4573585	HRPEpiC	eye:	n/a
34	chr7:4573535-4573585	MCF-7	breast:	n/a
35	chr7:4536864-4536914	AG04450	lung:	fetal
36	chr7:4573716-4573766	GM19239	blood:	n/a
37	chr7:4573535-4573585	AG04450	lung:	fetal
38	chr7:4573716-4573766	GM12878	blood:	n/a
39	chr7:4536864-4536914	NB4	blood:	n/a
40	chr7:4536838-4536888	SKMC	muscle:	n/a
41	chr7:4630518-4630568	HCPEpiC	choroid plexus:	n/a
42	chr7:4536838-4536888	NH-A	brain:	n/a
43	chr7:4573716-4573766	AG09319	gingival:	n/a
44	chr7:4573535-4573585	GM12891	blood:	n/a
45	chr7:4536838-4536888	PFSK-1	brain:	n/a
46	chr7:4573716-4573766	HEK293	kidney:	embryo
47	chr7:4573535-4573585	BJ	skin:	n/a
48	chr7:4536864-4536914	IMR90	lung:	fetal
49	chr7:4573716-4573766	CMK	blood:	n/a
50	chr7:4573716-4573766	BE2_C	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
2	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
3	chr7:4613003..4615813-chr7:4681464..4683495,2	MCF-7	breast:
4	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
5	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
6	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
7	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
8	chr7:4601107..4601677-chr7:4670928..4671456,2	MCF-7	breast:
9	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
10	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
11	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
12	chr20:52556259..52556926-chr7:4599215..4599761,2	MCF-7	breast:
13	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
14	chr15:101629167..101629860-chr7:4485245..4486227,2	MCF-7	breast:
15	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
16	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
17	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:
18	chr7:4642981..4645443-chr7:4649025..4651972,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863
2	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
3	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
4	lnc-SDK1-1	chr7:4482317-4482707	l_3355_chr7:4440443-4482707_testes

No data

Variant related genes	Relation type
CYP3A54P	TF binding region
CYP3A54P	CpG island
ENSG00000236352	chromatin interactions
ENSG00000164916	chromatin interactions
ENSG00000261809	chromatin interactions
VEGFA	miRNA target sites

Extended variants
information (count: 3088 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3088 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2034312	chr7:4477992-4477993	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573340628	chr7:4478062-4478063	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540536218	chr7:4478109-4478110	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78483462	chr7:4478164-4478165	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536408219	chr7:4478189-4478190	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571665603	chr7:4478193-4478194	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541019081	chr7:4478196-4478197	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560649936	chr7:4478199-4478200	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574261553	chr7:4478279-4478280	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542869479	chr7:4478296-4478297	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554816990	chr7:4478331-4478332	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7800491	chr7:4478339-4478340	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551861486	chr7:4478344-4478345	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2040919	chr7:4478357-4478358	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370053954	chr7:4478381-4478382	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71535113	chr7:4478385-4478386	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60880927	chr7:4478421-4478422	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57371170	chr7:4478422-4478423	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139923813	chr7:4478424-4478425	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542672534	chr7:4478446-4478447	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527728219	chr7:4478449-4478450	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550325753	chr7:4478451-4478452	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543059836	chr7:4478467-4478468	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549409266	chr7:4478468-4478469	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570063887	chr7:4478487-4478488	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547745095	chr7:4478491-4478492	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570505369	chr7:4478501-4478502	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200947450	chr7:4478510-4478511	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554609824	chr7:4478518-4478519	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147427908	chr7:4478529-4478530	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574400070	chr7:4478531-4478532	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559246792	chr7:4478561-4478562	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543345937	chr7:4478584-4478585	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558839629	chr7:4478586-4478587	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536510292	chr7:4478587-4478588	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7783362	chr7:4478588-4478589	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs553644926	chr7:4478591-4478592	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111211165	chr7:4478597-4478598	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191319429	chr7:4478608-4478609	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181214090	chr7:4478618-4478619	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567743774	chr7:4478619-4478620	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572085462	chr7:4478627-4478628	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368632119	chr7:4478629-4478630	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377179922	chr7:4478634-4478635	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562037216	chr7:4478662-4478663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574275026	chr7:4478668-4478669	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79610323	chr7:4478676-4478677	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145722185	chr7:4478683-4478684	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370197494	chr7:4478685-4478686	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576066134	chr7:4478690-4478691	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
early-passage human iPS cells	21368824	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4474600-4478200	Enhancers	Fetal Intestine Small	intestine
2	chr7:4475600-4478200	Enhancers	Fetal Intestine Large	intestine
3	chr7:4477000-4478200	Enhancers	Fetal Muscle Leg	muscle
4	chr7:4478000-4479400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:4478200-4483400	Weak transcription	Fetal Intestine Small	intestine
6	chr7:4482200-4486000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr7:4483000-4483200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:4483400-4485000	Enhancers	Fetal Intestine Large	intestine
9	chr7:4483400-4485000	Enhancers	Fetal Intestine Small	intestine
10	chr7:4483600-4483800	Enhancers	Fetal Kidney	kidney
11	chr7:4483800-4485400	Weak transcription	Fetal Kidney	kidney
12	chr7:4485000-4488600	Weak transcription	Fetal Intestine Large	intestine
13	chr7:4485000-4488600	Weak transcription	Fetal Intestine Small	intestine
14	chr7:4485400-4485800	ZNF genes & repeats	Fetal Kidney	kidney
15	chr7:4485600-4485800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr7:4485800-4491400	Weak transcription	Fetal Kidney	kidney
17	chr7:4488600-4489400	Enhancers	HepG2	liver
18	chr7:4488600-4489600	Enhancers	Fetal Intestine Large	intestine
19	chr7:4488600-4489600	Enhancers	Fetal Intestine Small	intestine
20	chr7:4489000-4489600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:4497200-4498000	Enhancers	Fetal Muscle Trunk	muscle
22	chr7:4497400-4498200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:4497400-4498200	Enhancers	Adipose Nuclei	Adipose
24	chr7:4497400-4498600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:4497400-4498600	Enhancers	Fetal Muscle Leg	muscle
26	chr7:4497400-4498600	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr7:4497400-4498800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr7:4497400-4498800	Enhancers	Ovary	ovary
29	chr7:4497600-4498200	Enhancers	Brain Germinal Matrix	brain
30	chr7:4497600-4498200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr7:4497600-4498400	Enhancers	Colon Smooth Muscle	Colon
32	chr7:4497600-4498400	Enhancers	Fetal Brain Male	brain
33	chr7:4497600-4498600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:4497800-4498200	Enhancers	Fetal Brain Female	brain
35	chr7:4498000-4498600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
36	chr7:4498200-4498600	Enhancers	Brain Hippocampus Middle	brain
37	chr7:4498600-4500200	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr7:4498600-4500200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:4499600-4499800	Enhancers	Aorta	Aorta
40	chr7:4499800-4500600	Enhancers	Fetal Intestine Large	intestine
41	chr7:4499800-4502600	Weak transcription	Aorta	Aorta
42	chr7:4500200-4500600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:4500200-4500600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:4500200-4501200	Enhancers	Fetal Intestine Small	intestine
45	chr7:4500200-4502600	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr7:4500800-4501400	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr7:4501400-4501600	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr7:4501600-4501800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:4509000-4510000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr7:4509000-4510000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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