Variant report

Variant	nsv519574
Chromosome Location	chr14:63767811-63857808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:848)
CpG islands
(count:427)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:848 , 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	ATF2	chr14:63850463-63850949	GM12878	blood:	n/a	n/a
2	BACH1	chr14:63855832-63855875	K562	blood:	n/a	n/a
3	BATF	chr14:63837832-63838034	GM12878	blood:	n/a	n/a
4	BATF	chr14:63850478-63850694	GM12878	blood:	n/a	n/a
5	BATF	chr14:63837850-63838032	GM12878	blood:	n/a	n/a
6	BCL3	chr14:63829151-63829554	GM12878	blood:	n/a	n/a
7	BCL3	chr14:63827695-63827949	GM12878	blood:	n/a	n/a
8	BCL3	chr14:63829154-63829566	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:63855463-63855787	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr14:63782321-63782360	GM12878	blood:	n/a	n/a
11	CEBPB	chr14:63842444-63843021	IMR90	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
12	CEBPB	chr14:63842579-63842902	K562	blood:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
13	CEBPB	chr14:63835079-63835317	HepG2	liver:	n/a	chr14:63835165-63835176
14	CEBPB	chr14:63798489-63798718	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:63820978-63821201	HepG2	liver:	n/a	chr14:63821071-63821082
16	CEBPB	chr14:63842462-63842947	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
17	CEBPB	chr14:63842433-63843010	Hela-S3	cervix:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
18	CEBPB	chr14:63826972-63827278	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:63834999-63835300	A549	lung:	n/a	chr14:63835165-63835176
20	CEBPB	chr14:63842470-63842926	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
21	CEBPB	chr14:63809144-63809428	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:63842540-63842810	H1-hESC	embryonic stem cell:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
23	CEBPB	chr14:63835037-63835278	K562	blood:	n/a	chr14:63835165-63835176
24	CEBPB	chr14:63790310-63790386	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:63774427-63774613	IMR90	lung:	n/a	n/a
26	CEBPB	chr14:63782893-63783093	A549	lung:	n/a	n/a
27	CEBPB	chr14:63842544-63842804	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
28	CEBPB	chr14:63835034-63835323	IMR90	lung:	n/a	chr14:63835165-63835176
29	CEBPB	chr14:63845972-63846129	MCF-7	breast:	n/a	chr14:63846045-63846056
30	CEBPB	chr14:63798372-63798717	A549	lung:	n/a	n/a
31	CEBPB	chr14:63798403-63798684	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:63842570-63842689	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
33	CEBPB	chr14:63798468-63798578	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:63809186-63809476	A549	lung:	n/a	n/a
35	CEBPB	chr14:63846009-63846069	HepG2	liver:	n/a	chr14:63846045-63846056
36	CEBPB	chr14:63842517-63842730	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
37	CEBPB	chr14:63842449-63843004	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
38	CEBPB	chr14:63842418-63842898	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
39	CHD2	chr14:63842557-63842804	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:63810023-63810048	HepG2	liver:	n/a	n/a
41	CHD2	chr14:63855550-63855774	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr14:63855608-63855801	A549	lung:	n/a	n/a
43	CTCF	chr14:63828585-63828801	MCF-7	breast:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
44	CTCF	chr14:63828662-63828744	GM10266	blood:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
45	CTCF	chr14:63855640-63855790	GM12866	blood:	n/a	n/a
46	CTCF	chr14:63775511-63775807	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:63855680-63855830	RPTEC	kidney:	n/a	n/a
48	CTCF	chr14:63855640-63855790	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr14:63775555-63775738	GM20000	blood:	n/a	n/a
50	CTCF	chr14:63834560-63834710	NHEK	skin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:63784394-63784444	CMK	blood:	n/a
2	chr14:63781994-63782044	HL-60	blood:	n/a
3	chr14:63785287-63785337	GM12891	blood:	n/a
4	chr14:63785287-63785337	Caco-2	colon:	n/a
5	chr14:63785334-63785384	ProgFib	skin:	n/a
6	chr14:63785287-63785337	SK-N-MC	brain:	n/a
7	chr14:63784394-63784444	MCF-7	breast:	n/a
8	chr14:63785523-63785573	BE2_C	brain:	n/a
9	chr14:63781994-63782044	HCM	heart:	n/a
10	chr14:63784574-63784624	HIPEpiC	eye:	n/a
11	chr14:63784394-63784444	NH-A	brain:	n/a
12	chr14:63784394-63784444	SK-N-SH_RA	brain:	n/a
13	chr14:63784394-63784444	AG09309	skin:	n/a
14	chr14:63781994-63782044	SAEC	small airway:	n/a
15	chr14:63781994-63782044	HNPCEpiC	eye:	n/a
16	chr14:63781994-63782044	HAEpiC	amniotic membrane:	n/a
17	chr14:63785287-63785337	NHDF-neo	bronchial:	n/a
18	chr14:63785334-63785384	HAEpiC	amniotic membrane:	n/a
19	chr14:63784574-63784624	NT2-D1	testis:	n/a
20	chr14:63785523-63785573	AG04450	lung:	fetal
21	chr14:63779694-63779744	PANC-1	pancreas:	n/a
22	chr14:63779694-63779744	GM12891	blood:	n/a
23	chr14:63785287-63785337	SAEC	small airway:	n/a
24	chr14:63779694-63779744	NHBE	bronchial:	n/a
25	chr14:63785334-63785384	HMEC	breast:	n/a
26	chr14:63785287-63785337	HRE	kidney:	n/a
27	chr14:63781994-63782044	SK-N-SH	brain:	n/a
28	chr14:63785287-63785337	CMK	blood:	n/a
29	chr14:63781994-63782044	Hepatocyte	liver:	n/a
30	chr14:63779694-63779744	GM06990	blood:	n/a
31	chr14:63785523-63785573	HCPEpiC	choroid plexus:	n/a
32	chr14:63781994-63782044	Caco-2	colon:	n/a
33	chr14:63784394-63784444	GM12878	blood:	n/a
34	chr14:63785287-63785337	PANC-1	pancreas:	n/a
35	chr14:63785523-63785573	HCT-116	colon:	n/a
36	chr14:63784394-63784444	HRE	kidney:	n/a
37	chr14:63784394-63784444	NT2-D1	testis:	n/a
38	chr14:63781994-63782044	T-47D	breast:	n/a
39	chr14:63781994-63782044	HEK293	kidney:	embryo
40	chr14:63785287-63785337	NT2-D1	testis:	n/a
41	chr14:63781994-63782044	K562	blood:	n/a
42	chr14:63779694-63779744	HEEpiC	esophagus:	n/a
43	chr14:63785287-63785337	AG09309	skin:	n/a
44	chr14:63781994-63782044	MCF-7	breast:	n/a
45	chr14:63784574-63784624	HepG2	liver:	n/a
46	chr14:63781994-63782044	LNCaP	prostate:	n/a
47	chr14:63785523-63785573	ECC-1	luminal epithelium:	n/a
48	chr14:63784394-63784444	MCF10A-Er-Src	breast:	n/a
49	chr14:63784394-63784444	AG10803	skin:	n/a
50	chr14:63785334-63785384	GM12891	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
2	chr14:63848595..63851169-chr14:64107183..64109145,2	K562	blood:
3	chr14:63855376..63856976-chr14:64105685..64108470,2	K562	blood:
4	chr14:62629724..62631701-chr14:63774617..63777066,2	MCF-7	breast:
5	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
6	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
7	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
8	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
9	chr14:63836099..63836920-chr6:128541621..128542384,2	MCF-7	breast:
10	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
11	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
12	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
13	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
14	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
15	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
16	chr14:63641198..63641930-chr14:63775163..63776037,2	MCF-7	breast:
17	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
18	chr14:63855376..63858099-chr14:64105447..64108157,3	K562	blood:
19	chr14:63855569..63857925-chr14:64009617..64011888,2	MCF-7	breast:
20	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
21	chr14:62629876..62630378-chr14:63775161..63775717,2	MCF-7	breast:
22	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
23	chr14:63775157..63776075-chr14:64011101..64011670,2	MCF-7	breast:
24	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
25	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
26	chr14:63784531..63787249-chr14:63793902..63795892,2	MCF-7	breast:
27	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
28	chr14:63855385..63856181-chr14:64010817..64012064,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258943	TF binding region
GPHB5	TF binding region
ENSG00000258943	CpG island
GPHB5	CpG island
ENSG00000154001	chromatin interactions
ENSG00000140006	chromatin interactions
ENSG00000179600	chromatin interactions
ENSG00000261242	chromatin interactions

Extended variants
information (count: 2504 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10483770	chr14:63767811-63767812	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78980493	chr14:63767815-63767816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537449611	chr14:63767850-63767851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557343132	chr14:63767867-63767868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10139597	chr14:63767880-63767881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs180833478	chr14:63767936-63767937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138720412	chr14:63767953-63767954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200333319	chr14:63767992-63767993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572182599	chr14:63768025-63768026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148937863	chr14:63768082-63768083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80126892	chr14:63768095-63768096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574154144	chr14:63768113-63768114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143585455	chr14:63768123-63768124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148065843	chr14:63768140-63768141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143580710	chr14:63768146-63768147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185098046	chr14:63768167-63768168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190727763	chr14:63768168-63768169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528685471	chr14:63768204-63768205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548755904	chr14:63768215-63768216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76141533	chr14:63768217-63768218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1955672	chr14:63768223-63768224	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541479041	chr14:63768274-63768275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373486783	chr14:63768275-63768276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147194601	chr14:63768290-63768291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77730299	chr14:63768450-63768451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551009234	chr14:63768486-63768487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570809836	chr14:63768493-63768494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538584570	chr14:63768494-63768495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115845037	chr14:63768540-63768541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370022018	chr14:63768615-63768616	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs565777613	chr14:63768652-63768653	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs114339164	chr14:63768666-63768667	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs554298427	chr14:63768718-63768719	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs574216451	chr14:63768753-63768754	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs543081126	chr14:63768793-63768794	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556718827	chr14:63768841-63768842	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183935343	chr14:63768846-63768847	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs10142953	chr14:63768905-63768906	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560001377	chr14:63768960-63768961	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186849763	chr14:63768990-63768991	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs563425954	chr14:63768993-63768994	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs568489266	chr14:63768999-63769000	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs57081610	chr14:63769014-63769015	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs368913406	chr14:63769026-63769027	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370072185	chr14:63769062-63769063	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs191483505	chr14:63769224-63769225	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs34175610	chr14:63769320-63769321	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs7149568	chr14:63769333-63769334	Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142748952	chr14:63769401-63769402	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs4027889	chr14:63769416-63769417	Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22737080	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:847 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63740800-63768000	Weak transcription	Right Ventricle	heart
2	chr14:63762600-63768200	Weak transcription	Left Ventricle	heart
3	chr14:63763400-63768000	Weak transcription	Fetal Heart	heart
4	chr14:63763800-63768200	Weak transcription	Fetal Muscle Leg	muscle
5	chr14:63764000-63768400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr14:63764000-63769000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr14:63764600-63768800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:63766200-63768000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr14:63766800-63768000	Weak transcription	Adipose Nuclei	Adipose
10	chr14:63767600-63768600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:63768000-63768200	Enhancers	Right Ventricle	heart
12	chr14:63768000-63768400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr14:63768000-63769200	Enhancers	Adipose Nuclei	Adipose
14	chr14:63768000-63769600	Enhancers	Fetal Heart	heart
15	chr14:63768200-63768600	Weak transcription	Right Ventricle	heart
16	chr14:63768200-63769200	Enhancers	Fetal Muscle Leg	muscle
17	chr14:63768200-63769200	Enhancers	Left Ventricle	heart
18	chr14:63768400-63768600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:63768400-63769200	Enhancers	Fetal Muscle Trunk	muscle
20	chr14:63768600-63769000	Enhancers	Right Ventricle	heart
21	chr14:63768600-63769200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:63768600-63769200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr14:63768600-63769600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr14:63768800-63769000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr14:63768800-63769200	Enhancers	Right Atrium	heart
26	chr14:63768800-63769400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:63769000-63769200	Enhancers	Brain Hippocampus Middle	brain
28	chr14:63772600-63777200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr14:63774800-63775400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:63775000-63775200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr14:63777200-63779000	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr14:63779600-63780400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:63779800-63780000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr14:63779800-63780200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr14:63780000-63780400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:63784200-63784600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:63789000-63790800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr14:63789200-63790200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:63789200-63790400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:63789400-63790200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr14:63789400-63790200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr14:63789600-63790000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:63789800-63790400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr14:63790000-63790400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr14:63790000-63790400	Enhancers	Fetal Muscle Leg	muscle
46	chr14:63790000-63790600	Enhancers	Fetal Brain Male	brain
47	chr14:63793400-63794400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:63795000-63797200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:63797200-63799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:63799600-63799800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links