Variant report

Variant	esv2751279
Chromosome Location	chr14:63754363-63871416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:996)
CpG islands
(count:488)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	ATF2	chr14:63762661-63763221	GM12878	blood:	n/a	n/a
3	BACH1	chr14:63855832-63855875	K562	blood:	n/a	n/a
4	BATF	chr14:63850478-63850694	GM12878	blood:	n/a	n/a
5	BATF	chr14:63837832-63838034	GM12878	blood:	n/a	n/a
6	BATF	chr14:63762637-63763050	GM12878	blood:	n/a	chr14:63762839-63762850
7	BATF	chr14:63837850-63838032	GM12878	blood:	n/a	n/a
8	BATF	chr14:63755626-63755883	GM12878	blood:	n/a	n/a
9	BATF	chr14:63762679-63763006	GM12878	blood:	n/a	chr14:63762839-63762850
10	BATF	chr14:63867907-63868096	GM12878	blood:	n/a	chr14:63868005-63868016
11	BATF	chr14:63865575-63865812	GM12878	blood:	n/a	chr14:63865706-63865717
12	BATF	chr14:63865499-63865864	GM12878	blood:	n/a	chr14:63865706-63865717
13	BCL3	chr14:63829154-63829566	GM12878	blood:	n/a	n/a
14	BCL3	chr14:63829151-63829554	GM12878	blood:	n/a	n/a
15	BCL3	chr14:63827695-63827949	GM12878	blood:	n/a	n/a
16	BCL3	chr14:63762646-63763379	GM12878	blood:	n/a	n/a
17	BRCA1	chr14:63765282-63765300	GM12878	blood:	n/a	n/a
18	BRCA1	chr14:63782321-63782360	GM12878	blood:	n/a	n/a
19	BRCA1	chr14:63855463-63855787	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:63782893-63783093	A549	lung:	n/a	n/a
21	CEBPB	chr14:63809186-63809476	A549	lung:	n/a	n/a
22	CEBPB	chr14:63798489-63798718	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:63754737-63754937	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:63842462-63842947	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
25	CEBPB	chr14:63842470-63842926	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
26	CEBPB	chr14:63845972-63846129	MCF-7	breast:	n/a	chr14:63846045-63846056
27	CEBPB	chr14:63798372-63798717	A549	lung:	n/a	n/a
28	CEBPB	chr14:63842540-63842810	H1-hESC	embryonic stem cell:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
29	CEBPB	chr14:63774427-63774613	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:63798403-63798684	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:63835034-63835323	IMR90	lung:	n/a	chr14:63835165-63835176
32	CEBPB	chr14:63820978-63821201	HepG2	liver:	n/a	chr14:63821071-63821082
33	CEBPB	chr14:63826972-63827278	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:63842579-63842902	K562	blood:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
35	CEBPB	chr14:63834999-63835300	A549	lung:	n/a	chr14:63835165-63835176
36	CEBPB	chr14:63798468-63798578	Hela-S3	cervix:	n/a	n/a
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	CEBPB	chr14:63835079-63835317	HepG2	liver:	n/a	chr14:63835165-63835176
40	CEBPB	chr14:63842517-63842730	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
41	CEBPB	chr14:63846009-63846069	HepG2	liver:	n/a	chr14:63846045-63846056
42	CEBPB	chr14:63842444-63843021	IMR90	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
43	CEBPB	chr14:63835037-63835278	K562	blood:	n/a	chr14:63835165-63835176
44	CEBPB	chr14:63809144-63809428	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:63842570-63842689	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
46	CEBPB	chr14:63842544-63842804	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
47	CEBPB	chr14:63790310-63790386	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:63842433-63843010	Hela-S3	cervix:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
49	CHD2	chr14:63810023-63810048	HepG2	liver:	n/a	n/a
50	CHD2	chr14:63842557-63842804	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:63785334-63785384	SK-N-MC	brain:	n/a
2	chr14:63757917-63757967	GM12892	blood:	n/a
3	chr14:63784574-63784624	ProgFib	skin:	n/a
4	chr14:63757917-63757967	SK-N-SH	brain:	n/a
5	chr14:63785287-63785337	GM06990	blood:	n/a
6	chr14:63784574-63784624	AoSMC	blood vessel:	n/a
7	chr14:63784574-63784624	MCF-7	breast:	n/a
8	chr14:63785523-63785573	GM12891	blood:	n/a
9	chr14:63785287-63785337	CMK	blood:	n/a
10	chr14:63785334-63785384	GM12878	blood:	n/a
11	chr14:63784574-63784624	HUVEC	blood vessel:	n/a
12	chr14:63781994-63782044	Caco-2	colon:	n/a
13	chr14:63779694-63779744	ProgFib	skin:	n/a
14	chr14:63785523-63785573	BJ	skin:	n/a
15	chr14:63785287-63785337	ECC-1	luminal epithelium:	n/a
16	chr14:63781994-63782044	GM12892	blood:	n/a
17	chr14:63785523-63785573	ProgFib	skin:	n/a
18	chr14:63779694-63779744	HRCEpiC	kidney:	n/a
19	chr14:63784574-63784624	BJ	skin:	n/a
20	chr14:63781994-63782044	GM06990	blood:	n/a
21	chr14:63784394-63784444	HEK293	kidney:	embryo
22	chr14:63784394-63784444	AG10803	skin:	n/a
23	chr14:63779694-63779744	HNPCEpiC	eye:	n/a
24	chr14:63781994-63782044	SKMC	muscle:	n/a
25	chr14:63781994-63782044	NH-A	brain:	n/a
26	chr14:63757917-63757967	MCF10A-Er-Src	breast:	n/a
27	chr14:63784574-63784624	NB4	blood:	n/a
28	chr14:63757917-63757967	Hepatocyte	liver:	n/a
29	chr14:63785287-63785337	AG10803	skin:	n/a
30	chr14:63785334-63785384	AoSMC	blood vessel:	n/a
31	chr14:63757917-63757967	AG09309	skin:	n/a
32	chr14:63781994-63782044	MCF-7	breast:	n/a
33	chr14:63781994-63782044	AG09309	skin:	n/a
34	chr14:63784394-63784444	BJ	skin:	n/a
35	chr14:63785523-63785573	PFSK-1	brain:	n/a
36	chr14:63781994-63782044	HRCEpiC	kidney:	n/a
37	chr14:63757917-63757967	AG04449	skin:	fetal
38	chr14:63757917-63757967	LNCaP	prostate:	n/a
39	chr14:63781994-63782044	SK-N-MC	brain:	n/a
40	chr14:63785523-63785573	HUVEC	blood vessel:	n/a
41	chr14:63757917-63757967	MCF-7	breast:	n/a
42	chr14:63785287-63785337	HCM	heart:	n/a
43	chr14:63785523-63785573	ovcar-3	ovarian:	n/a
44	chr14:63784394-63784444	GM06990	blood:	n/a
45	chr14:63781994-63782044	HCPEpiC	choroid plexus:	n/a
46	chr14:63785523-63785573	Jurkat	blood:	n/a
47	chr14:63779694-63779744	GM12892	blood:	n/a
48	chr14:63784574-63784624	PANC-1	pancreas:	n/a
49	chr14:63779694-63779744	AG04450	lung:	fetal
50	chr14:63784574-63784624	HAEpiC	amniotic membrane:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
2	chr14:63857974..63860690-chr14:63917148..63919988,2	MCF-7	breast:
3	chr14:63855569..63857925-chr14:64009617..64011888,2	MCF-7	breast:
4	chr14:63641198..63641930-chr14:63775163..63776037,2	MCF-7	breast:
5	chr14:62629724..62631701-chr14:63774617..63777066,2	MCF-7	breast:
6	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
7	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
8	chr14:63775157..63776075-chr14:64011101..64011670,2	MCF-7	breast:
9	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
10	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
11	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
12	chr14:63749402..63752016-chr14:63753123..63755149,2	K562	blood:
13	chr14:63784531..63787249-chr14:63793902..63795892,2	MCF-7	breast:
14	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
15	chr14:63858881..63861162-chr14:64008688..64011612,2	MCF-7	breast:
16	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
17	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
18	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
19	chr14:63855385..63856181-chr14:64010817..64012064,6	MCF-7	breast:
20	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
21	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
22	chr14:63749402..63752016-chr14:63753123..63755762,3	K562	blood:
23	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
24	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
25	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
26	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
27	chr14:63855376..63856976-chr14:64105685..64108470,2	K562	blood:
28	chr14:63855376..63858099-chr14:64105447..64108157,3	K562	blood:
29	chr14:62629876..62630378-chr14:63775161..63775717,2	MCF-7	breast:
30	chr14:63848595..63851169-chr14:64107183..64109145,2	K562	blood:
31	chr14:63836099..63836920-chr6:128541621..128542384,2	MCF-7	breast:
32	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
33	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
34	chr14:63866982..63869213-chr14:64008832..64010696,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R5E-2	chr14:63764844-63765498	ENSG00000258943
2	lnc-PPP2R5E-2	chr14:63766041-63766265	ENSG00000258943

No data

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

Extended variants
information (count: 3619 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3619 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10149326	chr14:63754363-63754364	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150267470	chr14:63754409-63754410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140310082	chr14:63754424-63754425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547559688	chr14:63754472-63754473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567342495	chr14:63754481-63754482	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139367265	chr14:63754499-63754500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183901536	chr14:63754503-63754504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569523862	chr14:63754540-63754541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541354420	chr14:63754580-63754581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573845549	chr14:63754598-63754599	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558810459	chr14:63754673-63754674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572335151	chr14:63754691-63754692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371224184	chr14:63754710-63754711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189732361	chr14:63754728-63754729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143182027	chr14:63754790-63754791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77050924	chr14:63754860-63754861	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563716077	chr14:63754869-63754870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530211933	chr14:63754870-63754871	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74840464	chr14:63754945-63754946	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577293875	chr14:63754964-63754965	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545347907	chr14:63754979-63754980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565173198	chr14:63754987-63754988	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180860323	chr14:63754990-63754991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547576331	chr14:63755017-63755018	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560874785	chr14:63755034-63755035	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529821202	chr14:63755073-63755074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549578141	chr14:63755088-63755089	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374971437	chr14:63755096-63755097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569669942	chr14:63755125-63755126	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367625330	chr14:63755143-63755144	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147511295	chr14:63755158-63755159	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184543038	chr14:63755173-63755174	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566023128	chr14:63755194-63755195	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534945657	chr14:63755210-63755211	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190441662	chr14:63755211-63755212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562644424	chr14:63755218-63755219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112091809	chr14:63755241-63755242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537585560	chr14:63755244-63755245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557153249	chr14:63755246-63755247	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17100987	chr14:63755254-63755255	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138355079	chr14:63755272-63755273	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553359032	chr14:63755283-63755284	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576161484	chr14:63755300-63755301	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544821244	chr14:63755324-63755325	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199764097	chr14:63755402-63755403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572376983	chr14:63755428-63755429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139384602	chr14:63755440-63755441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149587768	chr14:63755475-63755476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561154078	chr14:63755487-63755488	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372126122	chr14:63755508-63755509	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	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
Breast cancer	22737080	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22543975	CNVD
small cell lung cancer	17426248	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1374 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63716000-63754600	Weak transcription	Aorta	Aorta
2	chr14:63717400-63754800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:63730800-63766000	Weak transcription	Spleen	Spleen
4	chr14:63737200-63755400	Weak transcription	Fetal Intestine Large	intestine
5	chr14:63738000-63757800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr14:63739400-63759400	Weak transcription	Fetal Intestine Small	intestine
7	chr14:63740800-63755400	Weak transcription	Psoas Muscle	Psoas
8	chr14:63740800-63762800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr14:63740800-63768000	Weak transcription	Right Ventricle	heart
10	chr14:63741000-63757600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:63744000-63755400	Weak transcription	HMEC	breast
12	chr14:63744000-63757600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:63744000-63761800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:63747000-63757600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:63747000-63761200	Strong transcription	NH-A	brain
16	chr14:63747400-63760200	Strong transcription	HUVEC	blood vessel
17	chr14:63750400-63755800	Strong transcription	Left Ventricle	heart
18	chr14:63750600-63756600	Strong transcription	Fetal Muscle Trunk	muscle
19	chr14:63750600-63757600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr14:63750800-63757400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:63751400-63754800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:63751400-63762200	Weak transcription	Right Atrium	heart
23	chr14:63751600-63762400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr14:63752000-63757600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr14:63752000-63761600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr14:63752000-63762000	Weak transcription	Colon Smooth Muscle	Colon
27	chr14:63752200-63755800	Weak transcription	GM12878-XiMat	blood
28	chr14:63752200-63756400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr14:63752200-63760600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr14:63752200-63762000	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr14:63752400-63755200	Strong transcription	Ovary	ovary
32	chr14:63752400-63760400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:63752400-63760800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:63752800-63755400	Strong transcription	Fetal Lung	lung
35	chr14:63752800-63756200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr14:63753000-63754800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr14:63753000-63757400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr14:63753000-63757800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:63753000-63757800	Weak transcription	Pancreas	Pancrea
40	chr14:63753200-63754800	Weak transcription	Adipose Nuclei	Adipose
41	chr14:63753200-63755000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr14:63753200-63757600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr14:63753200-63757600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr14:63753200-63757600	Weak transcription	Lung	lung
45	chr14:63753200-63761400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr14:63753400-63754800	Weak transcription	Fetal Stomach	stomach
47	chr14:63753400-63757800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr14:63753600-63754400	Weak transcription	Fetal Muscle Leg	muscle
49	chr14:63753800-63755600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:63753800-63756200	Enhancers	NHDF-Ad	bronchial

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