Variant report

Variant	esv1793389
Chromosome Location	chr14:64346190-64457224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:306)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:64389861-64390320	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:64363042-64363316	HepG2	liver:	n/a	n/a
3	ATF2	chr14:64438881-64439493	GM12878	blood:	n/a	n/a
4	ATF2	chr14:64404909-64405807	GM12878	blood:	n/a	n/a
5	ATF2	chr14:64357956-64358497	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:64405179-64405599	GM12878	blood:	n/a	n/a
7	BATF	chr14:64404947-64405245	GM12878	blood:	n/a	n/a
8	BCL3	chr14:64404899-64405902	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:64407168-64407548	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:64405261-64405768	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:64360575-64360649	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr14:64389880-64390147	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr14:64423471-64423481	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:64363039-64363534	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr14:64360358-64360877	A549	lung:	n/a	n/a
16	CEBPB	chr14:64360351-64360887	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:64360407-64360780	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr14:64368144-64368546	Hela-S3	cervix:	n/a	chr14:64368319-64368330 chr14:64368319-64368332
19	CEBPB	chr14:64368148-64368514	IMR90	lung:	n/a	chr14:64368319-64368330 chr14:64368319-64368332
20	CEBPB	chr14:64372117-64372405	HepG2	liver:	n/a	chr14:64372260-64372271
21	CEBPB	chr14:64363189-64363443	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:64453815-64454299	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:64363196-64363525	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:64449168-64449171	A549	lung:	n/a	n/a
25	CEBPB	chr14:64389698-64390318	MCF-7	breast:	n/a	n/a
26	CEBPB	chr14:64449172-64449232	IMR90	lung:	n/a	chr14:64449188-64449199
27	CEBPB	chr14:64389715-64390067	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:64389659-64390254	A549	lung:	n/a	n/a
29	CEBPB	chr14:64372132-64372331	A549	lung:	n/a	chr14:64372260-64372271
30	CEBPB	chr14:64389396-64390319	MCF-7	breast:	n/a	n/a
31	CEBPB	chr14:64389592-64390239	A549	lung:	n/a	n/a
32	CEBPB	chr14:64362966-64363585	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr14:64453970-64454207	A549	lung:	n/a	n/a
34	CEBPB	chr14:64449143-64449323	H1-hESC	embryonic stem cell:	n/a	chr14:64449188-64449199
35	CEBPB	chr14:64398383-64398410	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:64389690-64390249	A549	lung:	n/a	n/a
37	CEBPB	chr14:64389354-64390262	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:64372119-64372415	IMR90	lung:	n/a	chr14:64372260-64372271
39	CEBPB	chr14:64420320-64420430	A549	lung:	n/a	n/a
40	CEBPB	chr14:64432306-64432512	HepG2	liver:	n/a	chr14:64432442-64432451
41	CEBPB	chr14:64368191-64368481	H1-hESC	embryonic stem cell:	n/a	chr14:64368319-64368330 chr14:64368319-64368332
42	CEBPB	chr14:64389836-64390246	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:64368222-64368470	A549	lung:	n/a	chr14:64368319-64368330 chr14:64368319-64368332
44	CEBPB	chr14:64389877-64390248	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:64449141-64449203	HepG2	liver:	n/a	chr14:64449188-64449199
46	CEBPB	chr14:64368256-64368497	HepG2	liver:	n/a	chr14:64368319-64368330 chr14:64368319-64368332
47	CEBPB	chr14:64389946-64390119	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:64363110-64363488	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr14:64453896-64454259	Hela-S3	cervix:	n/a	n/a
50	CHD1	chr14:64357596-64357739	H1-hESC	embryonic stem cell:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64364050-64364100	GM12892	blood:	n/a
2	chr14:64364050-64364100	GM12892	blood:	n/a
3	chr14:64364050-64364100	HepG2	liver:	n/a
4	chr14:64430230-64430280	NHBE	bronchial:	n/a
5	chr14:64357795-64357845	GM06990	blood:	n/a
6	chr14:64357795-64357845	K562	blood:	n/a
7	chr14:64364050-64364100	HEEpiC	esophagus:	n/a
8	chr14:64357795-64357845	HNPCEpiC	eye:	n/a
9	chr14:64364050-64364100	H1-hESC	embryonic stem cell:	embryo
10	chr14:64357795-64357845	NB4	blood:	n/a
11	chr14:64361272-64361322	HRPEpiC	eye:	n/a
12	chr14:64419267-64419317	AG04449	skin:	fetal
13	chr14:64430230-64430280	HEK293	kidney:	embryo
14	chr14:64430230-64430280	HRPEpiC	eye:	n/a
15	chr14:64364050-64364100	AG04450	lung:	fetal
16	chr14:64357795-64357845	Hela-S3	cervix:	n/a
17	chr14:64361272-64361322	NB4	blood:	n/a
18	chr14:64361272-64361322	MCF-7	breast:	n/a
19	chr14:64430230-64430280	AG09309	skin:	n/a
20	chr14:64361272-64361322	HRCEpiC	kidney:	n/a
21	chr14:64419267-64419317	NT2-D1	testis:	n/a
22	chr14:64430230-64430280	GM19239	blood:	n/a
23	chr14:64419267-64419317	SK-N-MC	brain:	n/a
24	chr14:64364050-64364100	AG10803	skin:	n/a
25	chr14:64364050-64364100	SAEC	small airway:	n/a
26	chr14:64419267-64419317	CMK	blood:	n/a
27	chr14:64419267-64419317	H1-hESC	embryonic stem cell:	embryo
28	chr14:64430230-64430280	HIPEpiC	eye:	n/a
29	chr14:64364050-64364100	GM06990	blood:	n/a
30	chr14:64364050-64364100	HL-60	blood:	n/a
31	chr14:64357795-64357845	NHDF-neo	bronchial:	n/a
32	chr14:64357795-64357845	RPTEC	kidney:	n/a
33	chr14:64357795-64357845	ProgFib	skin:	n/a
34	chr14:64430230-64430280	BJ	skin:	n/a
35	chr14:64364050-64364100	GM12891	blood:	n/a
36	chr14:64419267-64419317	HepG2	liver:	n/a
37	chr14:64357795-64357845	Caco-2	colon:	n/a
38	chr14:64357795-64357845	NH-A	brain:	n/a
39	chr14:64361272-64361322	HCF	heart:	n/a
40	chr14:64419267-64419317	HL-60	blood:	n/a
41	chr14:64357795-64357845	HCF	heart:	n/a
42	chr14:64364050-64364100	Hela-S3	cervix:	n/a
43	chr14:64357795-64357845	HCM	heart:	n/a
44	chr14:64419267-64419317	HCM	heart:	n/a
45	chr14:64361272-64361322	HCM	heart:	n/a
46	chr14:64430230-64430280	PrEC	prostate:	n/a
47	chr14:64364050-64364100	HIPEpiC	eye:	n/a
48	chr14:64364050-64364100	PANC-1	pancreas:	n/a
49	chr14:64361272-64361322	HRE	kidney:	n/a
50	chr14:64357795-64357845	T-47D	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:64319728..64320273-chr14:64389731..64390242,2	MCF-7	breast:
2	chr14:64350604..64352187-chr14:64354098..64356730,2	MCF-7	breast:
3	chr14:64350604..64352187-chr14:64354098..64356730,2	MCF-7	breast:
4	chr14:64407990..64410133-chr14:64411071..64414129,3	MCF-7	breast:
5	chr14:64319630..64322805-chr14:64362843..64364773,3	MCF-7	breast:
6	chr14:64319548..64321513-chr14:64388971..64391619,2	MCF-7	breast:
7	chr14:64387137..64389678-chr14:64400895..64402635,2	MCF-7	breast:
8	chr14:64349303..64352052-chr2:9373051..9375606,2	MCF-7	breast:
9	chr14:64383780..64386623-chr14:64390441..64393099,2	K562	blood:
10	chr14:64387137..64389678-chr14:64400895..64402635,2	MCF-7	breast:
11	chr14:64372158..64375131-chr14:64377283..64378855,2	MCF-7	breast:
12	chr14:64319794..64321904-chr14:64361235..64363695,2	MCF-7	breast:
13	chr14:64318407..64321279-chr14:64347175..64349139,2	MCF-7	breast:
14	chr14:64373323..64375325-chr14:64805642..64807746,2	MCF-7	breast:
15	chr14:64407990..64410133-chr14:64411071..64414129,3	MCF-7	breast:
16	chr14:64372158..64375131-chr14:64377283..64378855,2	MCF-7	breast:
17	chr14:64402738..64405329-chr14:64411303..64414012,2	MCF-7	breast:
18	chr14:64318653..64321289-chr14:64441036..64444017,2	MCF-7	breast:
19	chr14:64383780..64386623-chr14:64390441..64393099,2	K562	blood:
20	chr14:64319705..64321623-chr14:64382416..64385265,2	MCF-7	breast:
21	chr14:64344937..64346649-chr14:64804014..64806193,2	MCF-7	breast:
22	chr14:64350600..64353514-chr7:30543619..30546570,2	MCF-7	breast:
23	chr14:64402738..64405329-chr14:64411303..64414012,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYNE2	TF binding region
SYNE2	CpG island
ENSG00000140009	chromatin interactions
ENSG00000006625	chromatin interactions
ENSG00000054654	chromatin interactions
ENSG00000214770	chromatin interactions

Extended variants
information (count: 4211 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4211 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4459477	chr14:64346190-64346191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538829601	chr14:64346212-64346213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534816516	chr14:64346320-64346321	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372241211	chr14:64346337-64346338	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568237900	chr14:64346381-64346382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536995852	chr14:64346426-64346427	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182923619	chr14:64346454-64346455	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576394777	chr14:64346496-64346497	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545354889	chr14:64346497-64346498	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112868463	chr14:64346579-64346580	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187803520	chr14:64346599-64346600	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558734723	chr14:64346604-64346605	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572163333	chr14:64346606-64346607	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs193010208	chr14:64346615-64346616	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184322861	chr14:64346616-64346617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs375362981	chr14:64346617-64346618	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569690775	chr14:64346739-64346740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187967447	chr14:64346751-64346752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117990048	chr14:64346796-64346797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562583177	chr14:64346831-64346832	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531384482	chr14:64346848-64346849	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572149373	chr14:64346850-64346851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532032258	chr14:64346875-64346876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552156335	chr14:64346894-64346895	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559499631	chr14:64346935-64346936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538221555	chr14:64347046-64347047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4902251	chr14:64347090-64347091	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs116602573	chr14:64347103-64347104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568191811	chr14:64347136-64347137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114202047	chr14:64347137-64347138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554515891	chr14:64347198-64347199	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34222253	chr14:64347210-64347211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140809056	chr14:64347216-64347217	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34950190	chr14:64347217-64347218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140677964	chr14:64347223-64347224	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149447102	chr14:64347246-64347247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112511910	chr14:64347298-64347299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112376912	chr14:64347310-64347311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543258203	chr14:64347329-64347330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs61984063	chr14:64347390-64347391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141043853	chr14:64347417-64347418	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558566538	chr14:64347454-64347455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572102476	chr14:64347550-64347551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199500656	chr14:64347569-64347570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79511604	chr14:64347581-64347582	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75721952	chr14:64347583-64347584	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368702582	chr14:64347588-64347589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555029467	chr14:64347589-64347590	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576268635	chr14:64347599-64347600	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4902252	chr14:64347625-64347626	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2678 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64321400-64350200	Weak transcription	Fetal Stomach	stomach
2	chr14:64327400-64355200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr14:64327600-64360000	Weak transcription	Gastric	stomach
4	chr14:64331200-64356400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:64335200-64360000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:64336800-64362800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:64337000-64357200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:64337000-64365200	Weak transcription	Fetal Thymus	thymus
9	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
10	chr14:64338000-64353800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr14:64338000-64355200	Weak transcription	Primary B cells from cord blood	blood
12	chr14:64339400-64366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr14:64341000-64356400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:64341000-64357200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:64341200-64346200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:64341200-64348400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr14:64341200-64348600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr14:64341200-64348800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:64341200-64351000	Weak transcription	Right Ventricle	heart
20	chr14:64341200-64352200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr14:64341200-64352400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr14:64341200-64354000	Weak transcription	Dnd41	blood
23	chr14:64341200-64354800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr14:64341200-64356400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr14:64341200-64356400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr14:64341200-64356600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:64341200-64357000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr14:64341200-64357200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:64341200-64357200	Weak transcription	Fetal Lung	lung
30	chr14:64341200-64357200	Weak transcription	Fetal Muscle Leg	muscle
31	chr14:64341400-64352400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr14:64341400-64352600	Weak transcription	Stomach Mucosa	stomach
33	chr14:64341400-64356600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr14:64341400-64356600	Weak transcription	Fetal Kidney	kidney
35	chr14:64341400-64366800	Weak transcription	Primary T cells from cord blood	blood
36	chr14:64342000-64350800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr14:64342400-64348400	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr14:64342400-64350800	Weak transcription	Pancreas	Pancrea
39	chr14:64342400-64354800	Weak transcription	Aorta	Aorta
40	chr14:64342400-64357200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:64342600-64348600	Weak transcription	Placenta	Placenta
42	chr14:64342600-64352000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:64342600-64352400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr14:64342600-64357400	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr14:64342800-64351000	Weak transcription	Lung	lung
46	chr14:64342800-64351600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr14:64342800-64352400	Weak transcription	Adipose Nuclei	Adipose
48	chr14:64342800-64354200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr14:64342800-64357000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:64342800-64357200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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