Variant report

Variant	nsv1038627
Chromosome Location	chr14:78635498-78657912
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	CEBPB	chr14:78650991-78651296	IMR90	lung:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
2	CEBPB	chr14:78651005-78651295	HepG2	liver:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
3	CEBPB	chr14:78651010-78651309	H1-hESC	embryonic stem cell:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
4	CEBPB	chr14:78650956-78651401	A549	lung:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
5	CEBPB	chr14:78650949-78651362	MCF-7	breast:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
6	CEBPB	chr14:78650888-78651414	MCF-7	breast:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
7	CEBPB	chr14:78650983-78651323	A549	lung:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
8	CEBPB	chr14:78651002-78651321	Hela-S3	cervix:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
9	CEBPB	chr14:78651053-78651327	K562	blood:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
10	CEBPB	chr14:78650940-78651353	A549	lung:	n/a	chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651159-78651168 chr14:78651157-78651170 chr14:78651179-78651190
11	CTCF	chr14:78650960-78651110	GM12866	blood:	n/a	n/a
12	CTCF	chr14:78655765-78655806	Fibrobl	skin:	n/a	n/a
13	CTCF	chr14:78636722-78636809	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F4	chr14:78646847-78646932	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F6	chr14:78636555-78636998	H1-hESC	embryonic stem cell:	n/a	n/a
16	ELF1	chr14:78655714-78656021	GM12878	blood:	n/a	n/a
17	GATA2	chr14:78639269-78639506	SH-SY5Y	brain:	n/a	n/a
18	GTF2F1	chr14:78636644-78636908	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUN	chr14:78644334-78644524	HepG2	liver:	n/a	chr14:78644473-78644486
20	JUND	chr14:78644290-78644654	HepG2	liver:	n/a	chr14:78644623-78644635 chr14:78644625-78644633 chr14:78644624-78644634
21	JUND	chr14:78643492-78643688	HepG2	liver:	n/a	chr14:78643606-78643615
22	JUND	chr14:78644521-78644593	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAFF	chr14:78651725-78651965	HepG2	liver:	n/a	chr14:78651821-78651839 chr14:78651827-78651841
24	MAFK	chr14:78651659-78652004	HepG2	liver:	n/a	chr14:78651824-78651844 chr14:78651823-78651838 chr14:78651827-78651841 chr14:78651826-78651842 chr14:78651828-78651837 chr14:78651828-78651838
25	MAFK	chr14:78651764-78651978	IMR90	lung:	n/a	chr14:78651824-78651844 chr14:78651823-78651838 chr14:78651827-78651841 chr14:78651826-78651842 chr14:78651828-78651837 chr14:78651828-78651838
26	MAFK	chr14:78651722-78652013	HepG2	liver:	n/a	chr14:78651824-78651844 chr14:78651823-78651838 chr14:78651827-78651841 chr14:78651826-78651842 chr14:78651828-78651837 chr14:78651828-78651838
27	MAFK	chr14:78651779-78651889	K562	blood:	n/a	chr14:78651824-78651844 chr14:78651823-78651838 chr14:78651827-78651841 chr14:78651826-78651842 chr14:78651828-78651837 chr14:78651828-78651838
28	MAX	chr14:78636428-78636942	H1-hESC	embryonic stem cell:	n/a	chr14:78636667-78636677 chr14:78636557-78636567
29	MXI1	chr14:78641642-78641662	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr14:78651337-78651375	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr14:78636520-78636995	H1-neurons	neurons:	n/a	n/a
32	POLR2A	chr14:78638477-78638483	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr14:78644871-78644876	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr14:78636660-78636852	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr14:78636608-78636886	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:78636494-78637054	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr14:78636776-78636783	MCF-7	breast:	n/a	n/a
38	POLR2A	chr14:78636644-78636890	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr14:78636470-78636981	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr14:78652599-78653031	H1-neurons	neurons:	n/a	n/a
41	RAD21	chr14:78636468-78636999	H1-hESC	embryonic stem cell:	n/a	n/a
42	RAD21	chr14:78636568-78636927	H1-hESC	embryonic stem cell:	n/a	n/a
43	REST	chr14:78636248-78637588	H1-neurons	neurons:	n/a	chr14:78636664-78636677
44	REST	chr14:78656583-78656984	H1-neurons	neurons:	n/a	n/a
45	REST	chr14:78656450-78657060	H1-neurons	neurons:	n/a	n/a
46	SIN3A	chr14:78636589-78636969	H1-hESC	embryonic stem cell:	n/a	n/a
47	STAT1	chr14:78653516-78653520	GM12878	blood:	n/a	n/a
48	STAT3	chr14:78653277-78653344	MCF10A-Er-Src	breast:	n/a	n/a
49	TAF1	chr14:78636521-78636891	H1-hESC	embryonic stem cell:	n/a	n/a
50	TAF1	chr14:78636504-78636942	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78639767-78639817	NHBE	bronchial:	n/a
2	chr14:78640203-78640253	K562	blood:	n/a
3	chr14:78639736-78639786	AG04449	skin:	fetal
4	chr14:78639767-78639817	IMR90	lung:	fetal
5	chr14:78639736-78639786	CMK	blood:	n/a
6	chr14:78635905-78635955	HCM	heart:	n/a
7	chr14:78640203-78640253	RPTEC	kidney:	n/a
8	chr14:78639736-78639786	A549	lung:	n/a
9	chr14:78639736-78639786	NT2-D1	testis:	n/a
10	chr14:78635941-78635991	MCF-7	breast:	n/a
11	chr14:78639767-78639817	AG04449	skin:	fetal
12	chr14:78639736-78639786	GM12891	blood:	n/a
13	chr14:78635905-78635955	NHDF-neo	bronchial:	n/a
14	chr14:78635941-78635991	HNPCEpiC	eye:	n/a
15	chr14:78639767-78639817	SK-N-MC	brain:	n/a
16	chr14:78636730-78636780	Hela-S3	cervix:	n/a
17	chr14:78640203-78640253	PFSK-1	brain:	n/a
18	chr14:78639767-78639817	HRE	kidney:	n/a
19	chr14:78639736-78639786	BE2_C	brain:	n/a
20	chr14:78640203-78640253	PrEC	prostate:	n/a
21	chr14:78640203-78640253	LNCaP	prostate:	n/a
22	chr14:78639736-78639786	SK-N-SH_RA	brain:	n/a
23	chr14:78640203-78640253	HIPEpiC	eye:	n/a
24	chr14:78639736-78639786	Hela-S3	cervix:	n/a
25	chr14:78635905-78635955	Hepatocyte	liver:	n/a
26	chr14:78640203-78640253	AG04450	lung:	fetal
27	chr14:78640203-78640253	ECC-1	luminal epithelium:	n/a
28	chr14:78635905-78635955	GM19239	blood:	n/a
29	chr14:78635941-78635991	ECC-1	luminal epithelium:	n/a
30	chr14:78636730-78636780	HL-60	blood:	n/a
31	chr14:78635905-78635955	HCT-116	colon:	n/a
32	chr14:78635941-78635991	GM12892	blood:	n/a
33	chr14:78639736-78639786	HCPEpiC	choroid plexus:	n/a
34	chr14:78640203-78640253	HUVEC	blood vessel:	n/a
35	chr14:78636730-78636780	HRCEpiC	kidney:	n/a
36	chr14:78639736-78639786	H1-hESC	embryonic stem cell:	embryo
37	chr14:78635941-78635991	AoSMC	blood vessel:	n/a
38	chr14:78636730-78636780	HRPEpiC	eye:	n/a
39	chr14:78636730-78636780	AG09319	gingival:	n/a
40	chr14:78635905-78635955	A549	lung:	n/a
41	chr14:78636730-78636780	SKMC	muscle:	n/a
42	chr14:78639767-78639817	Hepatocyte	liver:	n/a
43	chr14:78636730-78636780	AG09309	skin:	n/a
44	chr14:78635941-78635991	K562	blood:	n/a
45	chr14:78635905-78635955	HUVEC	blood vessel:	n/a
46	chr14:78635941-78635991	CMK	blood:	n/a
47	chr14:78639736-78639786	ovcar-3	ovarian:	n/a
48	chr14:78640203-78640253	BE2_C	brain:	n/a
49	chr14:78636730-78636780	HCPEpiC	choroid plexus:	n/a
50	chr14:78635905-78635955	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:120637014..120639131-chr14:78656980..78658480,2	MCF-7	breast:
2	chr14:78629719..78632310-chr14:78635472..78637600,2	K562	blood:
3	chr14:78656543..78658978-chr14:78666256..78667863,2	MCF-7	breast:

Variant related genes	Relation type
RNA5SP388	TF binding region
RNA5SP388	CpG island
ENSG00000089157	chromatin interactions
ENSG00000255857	chromatin interactions

Extended variants
information (count: 878 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10146353	chr14:78635498-78635499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73316357	chr14:78635590-78635591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111878591	chr14:78635591-78635592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146070298	chr14:78635628-78635629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539612932	chr14:78635644-78635645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569899074	chr14:78635674-78635675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7152518	chr14:78635689-78635690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535748300	chr14:78635704-78635705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372854904	chr14:78635739-78635740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560946079	chr14:78635742-78635743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113758218	chr14:78635813-78635814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571931123	chr14:78635868-78635869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540308196	chr14:78635906-78635907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557678510	chr14:78635916-78635917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553880146	chr14:78635927-78635928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112319451	chr14:78635941-78635942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374660899	chr14:78635942-78635943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545838284	chr14:78635946-78635947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368958319	chr14:78636000-78636001	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs201533458	chr14:78636029-78636030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562901956	chr14:78636064-78636065	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs543336265	chr14:78636077-78636078	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs531871493	chr14:78636141-78636142	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs72681717	chr14:78636192-78636193	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138859818	chr14:78636207-78636208	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115861720	chr14:78636267-78636268	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs213559	chr14:78636300-78636301	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570601673	chr14:78636327-78636328	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532955967	chr14:78636358-78636359	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs141477967	chr14:78636411-78636412	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs199506791	chr14:78636485-78636486	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs73316359	chr14:78636492-78636493	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150555182	chr14:78636614-78636615	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs549286786	chr14:78636667-78636668	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs565520857	chr14:78636669-78636670	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546330515	chr14:78636671-78636672	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs534545302	chr14:78636701-78636702	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529757527	chr14:78636741-78636742	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs546420077	chr14:78636755-78636756	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs199967701	chr14:78636757-78636758	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs566474591	chr14:78636771-78636772	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs576407988	chr14:78636790-78636791	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs538668948	chr14:78636825-78636826	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562402095	chr14:78636831-78636832	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73316362	chr14:78636843-78636844	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs375745113	chr14:78636853-78636854	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564674757	chr14:78636871-78636872	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192845103	chr14:78636883-78636884	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549869167	chr14:78636904-78636905	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563114932	chr14:78636932-78636933	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78624600-78635800	Weak transcription	Brain Germinal Matrix	brain
2	chr14:78630800-78636400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:78630800-78636800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:78631000-78635800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:78631000-78636400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:78631000-78636400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr14:78632400-78636800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:78635800-78636000	Enhancers	Brain Germinal Matrix	brain
9	chr14:78636000-78636200	Flanking Active TSS	Brain Germinal Matrix	brain
10	chr14:78636000-78636200	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:78636000-78636400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:78636000-78636400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr14:78636000-78636600	Enhancers	Brain Angular Gyrus	brain
14	chr14:78636200-78636400	Enhancers	Brain Hippocampus Middle	brain
15	chr14:78636200-78636600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr14:78636200-78636600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr14:78636200-78636600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:78636200-78636600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:78636200-78636600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr14:78636200-78636600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:78636200-78636600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr14:78636200-78636600	Enhancers	Brain Anterior Caudate	brain
23	chr14:78636200-78636600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr14:78636200-78636800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:78636200-78636800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:78636200-78636800	Enhancers	Brain Cingulate Gyrus	brain
27	chr14:78636200-78636800	Active TSS	Brain Germinal Matrix	brain
28	chr14:78636200-78636800	Enhancers	Lung	lung
29	chr14:78636200-78641800	Active TSS	Fetal Brain Female	brain
30	chr14:78636400-78636600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr14:78636400-78636600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr14:78636400-78636600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr14:78636400-78636800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:78636400-78636800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr14:78636400-78636800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:78636400-78636800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:78636400-78636800	Weak transcription	Brain Hippocampus Middle	brain
38	chr14:78636400-78636800	Enhancers	Fetal Brain Male	brain
39	chr14:78636400-78641400	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr14:78636600-78636800	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr14:78636600-78636800	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr14:78636600-78636800	Active TSS	Fetal Kidney	kidney
43	chr14:78636600-78636800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr14:78636600-78636800	Bivalent/Poised TSS	A549	lung
45	chr14:78636600-78637000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr14:78636600-78637000	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr14:78636600-78637000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:78636600-78637000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:78636600-78637000	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr14:78636600-78637000	Enhancers	Rectal Mucosa Donor 31	rectum

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