Variant report

Variant	nsv522007
Chromosome Location	chr7:4503389-4589812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:490)
CpG islands
(count:244)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:490 , 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	ARID3A	chr7:4573177-4573308	K562	blood:	n/a	n/a
2	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
4	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
5	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
6	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
7	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
8	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
9	CEBPB	chr7:4562189-4562372	K562	blood:	n/a	chr7:4562300-4562311
10	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
11	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
12	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
13	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
14	CEBPB	chr7:4585045-4585090	A549	lung:	n/a	n/a
15	CEBPB	chr7:4533878-4534018	HepG2	liver:	n/a	chr7:4533904-4533915
16	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
17	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
18	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
19	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037
20	CEBPB	chr7:4543419-4543508	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
22	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
23	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
24	CEBPB	chr7:4584957-4585000	HepG2	liver:	n/a	chr7:4584972-4584983
25	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
26	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
27	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
28	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
29	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
30	CEBPD	chr7:4572950-4573325	K562	blood:	n/a	n/a
31	CEBPD	chr7:4573063-4573272	K562	blood:	n/a	n/a
32	CHD1	chr7:4541262-4541349	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr7:4519143-4519145	GM12878	blood:	n/a	n/a
34	CHD2	chr7:4540385-4540761	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:4573126-4573556	K562	blood:	n/a	n/a
36	CHD2	chr7:4573233-4573376	HepG2	liver:	n/a	n/a
37	CTCF	chr7:4519068-4519379	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:4519130-4519292	Fibrobl	skin:	n/a	n/a
39	CTCF	chr7:4512477-4512713	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:4519140-4519290	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr7:4519144-4519331	ProgFib	skin:	n/a	n/a
42	CTCF	chr7:4543060-4543210	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr7:4519120-4519270	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:4519116-4519309	A549	lung:	n/a	n/a
45	CTCF	chr7:4519140-4519290	GM12864	blood:	n/a	n/a
46	CTCF	chr7:4519243-4519262	GM19240	blood:	n/a	n/a
47	CTCF	chr7:4543040-4543190	GM12873	blood:	n/a	n/a
48	CTCF	chr7:4519044-4519372	T-47D	breast:	n/a	n/a
49	CTCF	chr7:4543026-4543227	K562	blood:	n/a	n/a
50	CTCF	chr7:4518991-4519400	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4536838-4536888	NT2-D1	testis:	n/a
2	chr7:4536838-4536888	SK-N-MC	brain:	n/a
3	chr7:4573716-4573766	IMR90	lung:	fetal
4	chr7:4573535-4573585	Jurkat	blood:	n/a
5	chr7:4573716-4573766	A549	lung:	n/a
6	chr7:4536864-4536914	GM19239	blood:	n/a
7	chr7:4536838-4536888	Hela-S3	cervix:	n/a
8	chr7:4573535-4573585	RPTEC	kidney:	n/a
9	chr7:4536864-4536914	HCM	heart:	n/a
10	chr7:4573535-4573585	HL-60	blood:	n/a
11	chr7:4536838-4536888	BE2_C	brain:	n/a
12	chr7:4573535-4573585	NB4	blood:	n/a
13	chr7:4573716-4573766	HRCEpiC	kidney:	n/a
14	chr7:4573716-4573766	ECC-1	luminal epithelium:	n/a
15	chr7:4536864-4536914	MCF-7	breast:	n/a
16	chr7:4573716-4573766	AoSMC	blood vessel:	n/a
17	chr7:4536838-4536888	H1-hESC	embryonic stem cell:	embryo
18	chr7:4536864-4536914	AG09309	skin:	n/a
19	chr7:4536838-4536888	GM12891	blood:	n/a
20	chr7:4536864-4536914	NB4	blood:	n/a
21	chr7:4573535-4573585	HCF	heart:	n/a
22	chr7:4573535-4573585	PrEC	prostate:	n/a
23	chr7:4573535-4573585	GM19239	blood:	n/a
24	chr7:4536864-4536914	HRPEpiC	eye:	n/a
25	chr7:4573535-4573585	IMR90	lung:	fetal
26	chr7:4573535-4573585	NH-A	brain:	n/a
27	chr7:4573535-4573585	U87	brain:	n/a
28	chr7:4573535-4573585	NHBE	bronchial:	n/a
29	chr7:4536838-4536888	HRE	kidney:	n/a
30	chr7:4536864-4536914	HRE	kidney:	n/a
31	chr7:4536838-4536888	ECC-1	luminal epithelium:	n/a
32	chr7:4536838-4536888	MCF-7	breast:	n/a
33	chr7:4536864-4536914	IMR90	lung:	fetal
34	chr7:4573716-4573766	GM06990	blood:	n/a
35	chr7:4573716-4573766	NH-A	brain:	n/a
36	chr7:4573716-4573766	HMEC	breast:	n/a
37	chr7:4536838-4536888	A549	lung:	n/a
38	chr7:4536838-4536888	GM12878	blood:	n/a
39	chr7:4573716-4573766	BJ	skin:	n/a
40	chr7:4573716-4573766	HL-60	blood:	n/a
41	chr7:4573535-4573585	CMK	blood:	n/a
42	chr7:4573535-4573585	H1-hESC	embryonic stem cell:	embryo
43	chr7:4536838-4536888	Caco-2	colon:	n/a
44	chr7:4536838-4536888	HNPCEpiC	eye:	n/a
45	chr7:4536864-4536914	U87	brain:	n/a
46	chr7:4573716-4573766	AG04449	skin:	fetal
47	chr7:4573716-4573766	HRE	kidney:	n/a
48	chr7:4573535-4573585	MCF-7	breast:	n/a
49	chr7:4573535-4573585	GM12878	blood:	n/a
50	chr7:4536864-4536914	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
2	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
3	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
4	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
5	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
6	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
7	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
8	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
9	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
10	chr7:4559356..4562288-chr7:4562408..4565136,2	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-RADIL-4	chr7:4513174-4513309	NONHSAT118863
2	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863
3	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972

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: 1039 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192688305	chr7:4509022-4509023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569866394	chr7:4509033-4509034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538781767	chr7:4509047-4509048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150094933	chr7:4509082-4509083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565681304	chr7:4509083-4509084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375635209	chr7:4509095-4509096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534292914	chr7:4509150-4509151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200585246	chr7:4509209-4509210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554204624	chr7:4509236-4509237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182998523	chr7:4509241-4509242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574283329	chr7:4509261-4509262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138642676	chr7:4509291-4509292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186670520	chr7:4509306-4509307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10216034	chr7:4509319-4509320	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545107534	chr7:4509328-4509329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192558299	chr7:4509347-4509348	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs371479019	chr7:4509367-4509368	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs527695580	chr7:4509371-4509372	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs184746833	chr7:4509400-4509401	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs189075844	chr7:4509411-4509412	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs529993303	chr7:4509466-4509467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372576369	chr7:4509468-4509469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550041841	chr7:4509516-4509517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549477634	chr7:4509552-4509553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141480664	chr7:4509589-4509590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532296466	chr7:4509613-4509614	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs552321456	chr7:4509614-4509615	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565744190	chr7:4509620-4509621	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs147009216	chr7:4509622-4509623	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs77985864	chr7:4509627-4509628	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs138159720	chr7:4509649-4509650	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs536582677	chr7:4509656-4509657	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs556398184	chr7:4509657-4509658	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs1466067	chr7:4509658-4509659	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs12155305	chr7:4509683-4509684	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs149511921	chr7:4509696-4509697	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs572477175	chr7:4509742-4509743	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs118179336	chr7:4509788-4509789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs193200120	chr7:4509819-4509820	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552729538	chr7:4509822-4509823	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530064987	chr7:4509825-4509826	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116304932	chr7:4509838-4509839	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563755251	chr7:4509845-4509846	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563544549	chr7:4509850-4509851	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532361182	chr7:4509859-4509860	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552432553	chr7:4509869-4509870	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143999568	chr7:4509896-4509897	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530921423	chr7:4509897-4509898	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548258796	chr7:4509900-4509901	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2343281	chr7:4509912-4509913	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
lymphocytic leukemia	21291569	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4509000-4510000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr7:4509000-4510000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:4509200-4509600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr7:4509200-4509800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr7:4509400-4509800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:4509400-4510000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:4509600-4510000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:4509600-4510000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr7:4509600-4510200	Enhancers	Aorta	Aorta
10	chr7:4509800-4513200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:4510000-4511200	Enhancers	Brain Germinal Matrix	brain
12	chr7:4510000-4512200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:4510000-4512200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:4510000-4512400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:4512200-4512400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:4512200-4513000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:4512200-4513000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:4512400-4512600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
19	chr7:4512400-4513000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr7:4512600-4512800	Enhancers	Adipose Nuclei	Adipose
21	chr7:4512600-4512800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr7:4513000-4513200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:4513000-4514600	Weak transcription	Adipose Nuclei	Adipose
24	chr7:4513200-4513600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:4513200-4513600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
26	chr7:4513600-4515400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:4514600-4515200	Enhancers	Adipose Nuclei	Adipose
28	chr7:4516400-4516800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
29	chr7:4523200-4524800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
30	chr7:4523400-4524600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:4524600-4525000	Enhancers	Adipose Nuclei	Adipose
32	chr7:4524800-4525200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr7:4539800-4540600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:4546600-4546800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:4559800-4560000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:4569800-4571000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:4570000-4570200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:4570200-4571000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:4570400-4571200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr7:4570600-4571000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr7:4570800-4571000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:4571000-4571200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr7:4571200-4571400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:4571200-4571400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr7:4571400-4571800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:4572200-4572400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:4572600-4572800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr7:4575600-4575800	Enhancers	Gastric	stomach
49	chr7:4575600-4576000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:4582400-4583000	ZNF genes & repeats	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links