Variant report

Variant	nsv1029296
Chromosome Location	chr7:4243652-4276004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4275147-4275340	HepG2	liver:	n/a	n/a
2	BACH1	chr7:4267463-4267573	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr7:4266133-4266382	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:4263384-4263667	HepG2	liver:	n/a	chr7:4263500-4263511
5	CEBPB	chr7:4266246-4266520	K562	blood:	n/a	chr7:4266338-4266349 chr7:4266336-4266349
6	CEBPB	chr7:4256123-4256127	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:4266196-4266361	HepG2	liver:	n/a	chr7:4266338-4266349 chr7:4266336-4266349
8	CEBPB	chr7:4266151-4266494	H1-hESC	embryonic stem cell:	n/a	chr7:4266338-4266349 chr7:4266336-4266349
9	CEBPB	chr7:4266105-4266576	MCF-7	breast:	n/a	chr7:4266338-4266349 chr7:4266336-4266349
10	CEBPB	chr7:4263377-4263614	IMR90	lung:	n/a	chr7:4263500-4263511
11	CEBPB	chr7:4263325-4263651	A549	lung:	n/a	chr7:4263500-4263511
12	CEBPB	chr7:4263419-4263579	K562	blood:	n/a	chr7:4263500-4263511
13	CEBPB	chr7:4263456-4263617	Hela-S3	cervix:	n/a	chr7:4263500-4263511
14	CEBPB	chr7:4266279-4266479	K562	blood:	n/a	chr7:4266338-4266349 chr7:4266336-4266349
15	CTCF	chr7:4266140-4266290	WERI-Rb-1	eye:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
16	CTCF	chr7:4266100-4266366	H1-hESC	embryonic stem cell:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
17	CTCF	chr7:4266100-4266250	MCF-7	breast:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
18	CTCF	chr7:4246680-4246830	NHEK	skin:	n/a	chr7:4246749-4246757
19	CTCF	chr7:4266140-4266290	HCT-116	colon:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
20	CTCF	chr7:4266182-4266318	MCF-7	breast:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
21	CTCF	chr7:4266120-4266270	HepG2	liver:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
22	CTCF	chr7:4266800-4266950	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:4266175-4266294	Hela-S3	cervix:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
24	CTCF	chr7:4266060-4266210	A549	lung:	n/a	n/a
25	CTCF	chr7:4266137-4266324	HepG2	liver:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
26	CTCF	chr7:4266120-4266270	SK-N-SH_RA	brain:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
27	CTCF	chr7:4264820-4264970	HepG2	liver:	n/a	n/a
28	CTCF	chr7:4244564-4244626	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:4266180-4266330	HEK293	kidney:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
30	CTCF	chr7:4266120-4266270	HCT-116	colon:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
31	CTCF	chr7:4266680-4266830	MCF-7	breast:	n/a	chr7:4266693-4266702
32	CTCF	chr7:4266020-4266170	RPTEC	kidney:	n/a	n/a
33	CTCF	chr7:4266180-4266330	NB4	blood:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
34	CTCF	chr7:4266160-4266310	NHEK	skin:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
35	CTCF	chr7:4266160-4266310	K562	blood:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
36	CTCF	chr7:4266109-4266346	K562	blood:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
37	CTCF	chr7:4266033-4266407	H1-hESC	embryonic stem cell:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
38	CTCF	chr7:4265780-4265930	K562	blood:	n/a	n/a
39	CTCF	chr7:4266180-4266330	NHEK	skin:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
40	CTCF	chr7:4266179-4266306	MCF-7	breast:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
41	CTCF	chr7:4255780-4255930	NHEK	skin:	n/a	n/a
42	CTCF	chr7:4266107-4266382	K562	blood:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
43	CTCF	chr7:4266155-4266315	MCF-7	breast:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
44	CTCF	chr7:4266120-4266270	MCF-7	breast:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
45	CTCF	chr7:4265994-4266324	H1-hESC	embryonic stem cell:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
46	CTCF	chr7:4266045-4266449	K562	blood:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
47	CTCF	chr7:4266200-4266350	HepG2	liver:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
48	CTCF	chr7:4266181-4266225	Medullo	brain:	n/a	n/a
49	CTCF	chr7:4266200-4266350	A549	lung:	n/a	chr7:4266222-4266235 chr7:4266220-4266236
50	CTCF	chr7:4255743-4255975	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4264980-4265030	NHBE	bronchial:	n/a
2	chr7:4255780-4255830	AG09319	gingival:	n/a
3	chr7:4250180-4250230	AG09319	gingival:	n/a
4	chr7:4254313-4254363	HRPEpiC	eye:	n/a
5	chr7:4264980-4265030	NHBE	bronchial:	n/a
6	chr7:4255780-4255830	AG09319	gingival:	n/a
7	chr7:4250180-4250230	AG09319	gingival:	n/a
8	chr7:4254313-4254363	HRPEpiC	eye:	n/a
9	chr7:4267364-4267414	GM19239	blood:	n/a
10	chr7:4267372-4267422	HUVEC	blood vessel:	n/a
11	chr7:4265548-4265598	SK-N-MC	brain:	n/a
12	chr7:4265548-4265598	GM12891	blood:	n/a
13	chr7:4267372-4267422	NHDF-neo	bronchial:	n/a
14	chr7:4250180-4250230	K562	blood:	n/a
15	chr7:4245514-4245564	GM19239	blood:	n/a
16	chr7:4254313-4254363	NT2-D1	testis:	n/a
17	chr7:4256914-4256964	BJ	skin:	n/a
18	chr7:4264980-4265030	SAEC	small airway:	n/a
19	chr7:4265272-4265322	Jurkat	blood:	n/a
20	chr7:4245492-4245542	ProgFib	skin:	n/a
21	chr7:4275924-4275974	K562	blood:	n/a
22	chr7:4250060-4250110	HUVEC	blood vessel:	n/a
23	chr7:4257254-4257304	RPTEC	kidney:	n/a
24	chr7:4243734-4243784	AG04449	skin:	fetal
25	chr7:4257050-4257100	MCF10A-Er-Src	breast:	n/a
26	chr7:4244372-4244422	AG09309	skin:	n/a
27	chr7:4244250-4244300	HMEC	breast:	n/a
28	chr7:4265468-4265518	HepG2	liver:	n/a
29	chr7:4244643-4244693	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:4267372-4267422	K562	blood:	n/a
31	chr7:4254796-4254846	AG04450	lung:	fetal
32	chr7:4254796-4254846	HRPEpiC	eye:	n/a
33	chr7:4255011-4255061	HCM	heart:	n/a
34	chr7:4245514-4245564	U87	brain:	n/a
35	chr7:4250060-4250110	AG10803	skin:	n/a
36	chr7:4256829-4256879	CMK	blood:	n/a
37	chr7:4250060-4250110	SK-N-MC	brain:	n/a
38	chr7:4254977-4255027	HL-60	blood:	n/a
39	chr7:4265468-4265518	LNCaP	prostate:	n/a
40	chr7:4247868-4247918	PFSK-1	brain:	n/a
41	chr7:4267364-4267414	HEEpiC	esophagus:	n/a
42	chr7:4249825-4249875	HCF	heart:	n/a
43	chr7:4250060-4250110	MCF-7	breast:	n/a
44	chr7:4245492-4245542	RPTEC	kidney:	n/a
45	chr7:4250180-4250230	NB4	blood:	n/a
46	chr7:4253955-4254005	NHBE	bronchial:	n/a
47	chr7:4265135-4265185	HEEpiC	esophagus:	n/a
48	chr7:4244372-4244422	Hela-S3	cervix:	n/a
49	chr7:4254313-4254363	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:4255011-4255061	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:4255812..4257721-chr7:4259160..4260933,2	MCF-7	breast:
2	chr7:4243767..4246398-chr7:4247420..4249656,2	MCF-7	breast:
3	chr7:4274876..4277578-chr7:4279083..4281112,2	K562	blood:
4	chr7:4255812..4257721-chr7:4259160..4260933,2	MCF-7	breast:
5	chr7:4243767..4246398-chr7:4247420..4249656,2	MCF-7	breast:
6	chr7:4243060..4244953-chr7:4246310..4247976,2	K562	blood:
7	chr7:4243060..4244953-chr7:4246310..4247976,2	K562	blood:
8	chr7:4240037..4242253-chr7:4255262..4257072,2	MCF-7	breast:
9	chr7:4265084..4267850-chr7:4273909..4275894,2	K562	blood:

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island
ENSG00000146555	chromatin interactions

Extended variants
information (count: 1998 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1998 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151171758	chr7:4243663-4243664	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs17134563	chr7:4243685-4243686	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs555310368	chr7:4243694-4243695	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs372152005	chr7:4243737-4243738	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs537267846	chr7:4243746-4243747	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs557391150	chr7:4243748-4243749	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs17134567	chr7:4243758-4243759	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs186105533	chr7:4243814-4243815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140187048	chr7:4243817-4243818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572938983	chr7:4243832-4243833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373094810	chr7:4243842-4243843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377237368	chr7:4243845-4243846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189392507	chr7:4243848-4243849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181640683	chr7:4243893-4243894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs17134570	chr7:4243897-4243898	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375196155	chr7:4243930-4243931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17134572	chr7:4243948-4243949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs527768058	chr7:4243956-4243957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564340852	chr7:4243957-4243958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372541510	chr7:4243960-4243961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532866267	chr7:4243961-4243962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375609478	chr7:4243962-4243963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560149385	chr7:4243967-4243968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371071410	chr7:4243987-4243988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117492139	chr7:4244010-4244011	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs548870692	chr7:4244011-4244012	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs568784890	chr7:4244018-4244019	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs564316765	chr7:4244027-4244028	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs550871320	chr7:4244040-4244041	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs571069492	chr7:4244063-4244064	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs146943239	chr7:4244070-4244071	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs375009701	chr7:4244108-4244109	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs77496158	chr7:4244125-4244126	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs191134387	chr7:4244135-4244136	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs183439276	chr7:4244136-4244137	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs28629320	chr7:4244138-4244139	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs367936852	chr7:4244140-4244141	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs111265758	chr7:4244142-4244143	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs116980031	chr7:4244152-4244153	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs544523794	chr7:4244155-4244156	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs564122695	chr7:4244166-4244167	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs186358991	chr7:4244169-4244170	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs13230809	chr7:4244185-4244186	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs117460909	chr7:4244193-4244194	Active TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs10264111	chr7:4244230-4244231	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs540282989	chr7:4244261-4244262	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs576880430	chr7:4244267-4244268	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs545570524	chr7:4244278-4244279	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs111637973	chr7:4244287-4244288	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs13231778	chr7:4244294-4244295	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4229400-4244400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr7:4229800-4268400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:4230000-4245600	Weak transcription	Pancreas	Pancrea
4	chr7:4235800-4287200	Weak transcription	Gastric	stomach
5	chr7:4240800-4246000	Weak transcription	Spleen	Spleen
6	chr7:4240800-4247400	Weak transcription	Aorta	Aorta
7	chr7:4241000-4244200	Weak transcription	Fetal Stomach	stomach
8	chr7:4241200-4243800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr7:4241600-4255400	Weak transcription	Esophagus	oesophagus
10	chr7:4242400-4244400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:4242400-4244800	Enhancers	Fetal Brain Male	brain
12	chr7:4242400-4247800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:4242600-4250000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:4242800-4243800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:4242800-4244200	Enhancers	Fetal Kidney	kidney
16	chr7:4242800-4267200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:4243000-4246400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:4243000-4247800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr7:4243000-4248400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:4243200-4243800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:4243400-4243800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:4243400-4243800	Enhancers	Fetal Brain Female	brain
23	chr7:4243400-4244000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr7:4243400-4244200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:4243400-4244600	Enhancers	Fetal Lung	lung
26	chr7:4243600-4243800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:4243600-4244200	Enhancers	Fetal Intestine Small	intestine
28	chr7:4243800-4244200	Enhancers	Fetal Heart	heart
29	chr7:4243800-4244200	Weak transcription	Fetal Intestine Large	intestine
30	chr7:4243800-4244400	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr7:4243800-4244800	Enhancers	Colon Smooth Muscle	Colon
32	chr7:4243800-4250600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:4243800-4266000	Weak transcription	Fetal Brain Female	brain
34	chr7:4244000-4244200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:4244000-4244200	Enhancers	Fetal Thymus	thymus
36	chr7:4244000-4244600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr7:4244000-4245000	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr7:4244000-4255000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr7:4244200-4244400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:4244200-4244400	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr7:4244200-4244600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:4244200-4244600	Flanking Active TSS	Fetal Intestine Small	intestine
43	chr7:4244200-4244600	Flanking Active TSS	Thymus	Thymus
44	chr7:4244200-4244800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr7:4244200-4244800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:4244200-4244800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr7:4244200-4244800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:4244200-4244800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:4244200-4244800	Active TSS	Fetal Intestine Large	intestine
50	chr7:4244200-4244800	Bivalent Enhancer	Fetal Muscle Leg	muscle

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