Variant report

Variant	nsv902369
Chromosome Location	chr14:104896538-104983655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:404)
CpG islands
(count:2201)
Chromatin interactive
region (count:36)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:104927523-104927809	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:104928581-104928716	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:104910308-104910836	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr14:104937880-104938837	GM12878	blood:	n/a	n/a
5	BCL3	chr14:104906905-104907311	GM12878	blood:	n/a	n/a
6	BCL3	chr14:104910404-104910832	GM12878	blood:	n/a	n/a
7	BCL3	chr14:104906971-104907201	GM12878	blood:	n/a	n/a
8	BCL3	chr14:104937869-104938923	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104910462-104910720	GM12878	blood:	n/a	n/a
10	CBX3	chr14:104948502-104948667	K562	blood:	n/a	n/a
11	CEBPB	chr14:104973877-104974075	K562	blood:	n/a	chr14:104974015-104974028
12	CEBPB	chr14:104929360-104929668	A549	lung:	n/a	n/a
13	CEBPB	chr14:104973932-104974132	HepG2	liver:	n/a	chr14:104974015-104974028
14	CEBPB	chr14:104927611-104927725	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:104954841-104955082	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:104929383-104929624	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:104929365-104929595	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:104973986-104973987	A549	lung:	n/a	n/a
19	CEBPB	chr14:104961481-104961670	A549	lung:	n/a	n/a
20	CHD2	chr14:104909120-104909319	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr14:104943728-104944011	A549	lung:	n/a	n/a
22	CTCF	chr14:104900280-104900430	GM12873	blood:	n/a	chr14:104900373-104900391
23	CTCF	chr14:104976100-104976250	GM12865	blood:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
24	CTCF	chr14:104900344-104900435	GM12878	blood:	n/a	chr14:104900373-104900391
25	CTCF	chr14:104939740-104939890	HEK293	kidney:	n/a	n/a
26	CTCF	chr14:104909880-104910030	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr14:104939591-104939832	H1-hESC	embryonic stem cell:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
28	CTCF	chr14:104939660-104939810	HepG2	liver:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
29	CTCF	chr14:104976100-104976250	HUVEC	blood vessel:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
30	CTCF	chr14:104976060-104976210	GM12875	blood:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
31	CTCF	chr14:104976156-104976222	Gliobla	brain:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
32	CTCF	chr14:104953600-104953750	HepG2	liver:	n/a	n/a
33	CTCF	chr14:104909842-104910089	K562	blood:	n/a	n/a
34	CTCF	chr14:104909932-104909972	MCF-7	breast:	n/a	n/a
35	CTCF	chr14:104900326-104900436	GM12891	blood:	n/a	chr14:104900373-104900391
36	CTCF	chr14:104976080-104976230	A549	lung:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
37	CTCF	chr14:104920787-104920790	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:104953640-104953790	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr14:104953649-104953761	Gliobla	brain:	n/a	n/a
40	CTCF	chr14:104976100-104976250	BE2_C	brain:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
41	CTCF	chr14:104928280-104928430	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr14:104900288-104900295	Lung_OC	lung:	n/a	n/a
43	CTCF	chr14:104953619-104953786	LNCaP	prostate:	n/a	n/a
44	CTCF	chr14:104909760-104909910	BE2_C	brain:	n/a	chr14:104909763-104909771
45	CTCF	chr14:104953617-104953751	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:104932060-104932210	GM12871	blood:	n/a	n/a
47	CTCF	chr14:104953630-104953752	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr14:104955838-104955934	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr14:104976060-104976210	GM12873	blood:	n/a	chr14:104976177-104976195 chr14:104976172-104976193
50	CTCF	chr14:104939502-104939898	H1-hESC	embryonic stem cell:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104917314-104917364	BJ	skin:	n/a
2	chr14:104928652-104928702	PrEC	prostate:	n/a
3	chr14:104925368-104925418	Hela-S3	cervix:	n/a
4	chr14:104979474-104979524	Jurkat	blood:	n/a
5	chr14:104917395-104917445	Jurkat	blood:	n/a
6	chr14:104917314-104917364	BJ	skin:	n/a
7	chr14:104928652-104928702	PrEC	prostate:	n/a
8	chr14:104925368-104925418	Hela-S3	cervix:	n/a
9	chr14:104979474-104979524	Jurkat	blood:	n/a
10	chr14:104917395-104917445	Jurkat	blood:	n/a
11	chr14:104979378-104979428	NHDF-neo	bronchial:	n/a
12	chr14:104979786-104979836	SK-N-MC	brain:	n/a
13	chr14:104928675-104928725	HCM	heart:	n/a
14	chr14:104940465-104940515	ECC-1	luminal epithelium:	n/a
15	chr14:104917314-104917364	Hepatocyte	liver:	n/a
16	chr14:104940465-104940515	SK-N-SH_RA	brain:	n/a
17	chr14:104937088-104937138	PFSK-1	brain:	n/a
18	chr14:104896560-104896610	Caco-2	colon:	n/a
19	chr14:104927127-104927177	PFSK-1	brain:	n/a
20	chr14:104931470-104931520	T-47D	breast:	n/a
21	chr14:104940939-104940989	AG10803	skin:	n/a
22	chr14:104896758-104896808	HNPCEpiC	eye:	n/a
23	chr14:104979378-104979428	T-47D	breast:	n/a
24	chr14:104980775-104980825	Hela-S3	cervix:	n/a
25	chr14:104931470-104931520	PFSK-1	brain:	n/a
26	chr14:104928472-104928522	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:104896560-104896610	HEK293	kidney:	embryo
28	chr14:104900453-104900503	GM06990	blood:	n/a
29	chr14:104897608-104897658	GM06990	blood:	n/a
30	chr14:104944443-104944493	NT2-D1	testis:	n/a
31	chr14:104979786-104979836	MCF10A-Er-Src	breast:	n/a
32	chr14:104979611-104979661	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:104940229-104940279	HCPEpiC	choroid plexus:	n/a
34	chr14:104928472-104928522	HEEpiC	esophagus:	n/a
35	chr14:104927127-104927177	AG04450	lung:	fetal
36	chr14:104940229-104940279	HRE	kidney:	n/a
37	chr14:104928055-104928105	ovcar-3	ovarian:	n/a
38	chr14:104928652-104928702	BE2_C	brain:	n/a
39	chr14:104940939-104940989	HRE	kidney:	n/a
40	chr14:104917314-104917364	PFSK-1	brain:	n/a
41	chr14:104979372-104979422	NHBE	bronchial:	n/a
42	chr14:104941923-104941973	GM12878	blood:	n/a
43	chr14:104979786-104979836	SK-N-SH	brain:	n/a
44	chr14:104896758-104896808	BE2_C	brain:	n/a
45	chr14:104896560-104896610	HUVEC	blood vessel:	n/a
46	chr14:104928652-104928702	AoSMC	blood vessel:	n/a
47	chr14:104897068-104897118	H1-hESC	embryonic stem cell:	embryo
48	chr14:104940229-104940279	HRPEpiC	eye:	n/a
49	chr14:104896488-104896538	CMK	blood:	n/a
50	chr14:104917314-104917364	GM12891	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
2	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
3	chr14:104972353..104974316-chr14:104979460..104981371,2	K562	blood:
4	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
5	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
6	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
7	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
8	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
9	chr14:104970856..104973249-chr14:104973750..104975351,2	MCF-7	breast:
10	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
11	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
12	chr14:104907745..104909314-chr14:105070369..105072440,2	MCF-7	breast:
13	chr14:104969493..104972414-chr14:104974399..104975982,2	K562	blood:
14	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
15	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
16	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
17	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
18	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
19	chr14:104972353..104974316-chr14:104979460..104981371,2	K562	blood:
20	chr14:104907597..104909438-chr14:105077013..105079589,2	K562	blood:
21	chr14:104747907..104749438-chr14:104962689..104965288,2	K562	blood:
22	chr14:104970856..104973249-chr14:104973750..104975351,2	MCF-7	breast:
23	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
24	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
25	chr14:104972522..104975026-chr14:104979915..104983932,3	MCF-7	breast:
26	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
27	chr14:104940339..104943047-chr14:104952341..104955339,2	MCF-7	breast:
28	chr14:104979670..104981888-chr16:405142..406765,2	MCF-7	breast:
29	chr14:104969493..104972414-chr14:104974399..104975982,2	K562	blood:
30	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
31	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
32	chr14:104915992..104918653-chr14:104925232..104927798,2	MCF-7	breast:
33	chr14:104917302..104919822-chr14:104924215..104925879,2	K562	blood:
34	chr14:104940339..104943047-chr14:104952341..104955339,2	MCF-7	breast:
35	chr14:104972522..104975026-chr14:104979915..104983932,3	MCF-7	breast:
36	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM179-7	chr14:104954502-104954773	l_1078_chr14:104952720-104954773_thyroid
2	lnc-TMEM179-7	chr14:104952721-104952755	l_1078_chr14:104952720-104954773_thyroid
3	lnc-TMEM179-6	chr14:104956064-104956198	l_1079_chr14:104954793-104957075_testes
4	lnc-TMEM179-7	chr14:104953909-104954474	l_1078_chr14:104952720-104954773_thyroid
5	lnc-TMEM179-6	chr14:104956321-104957075	l_1079_chr14:104954793-104957075_testes
6	lnc-TMEM179-5	chr14:104975962-104978198	NONHSAT040260
7	lnc-TMEM179-6	chr14:104954794-104955691	l_1079_chr14:104954793-104957075_testes

No data

Variant related genes	Relation type
CEND1P1	TF binding region
CEND1P1	CpG island
ENSG00000258986	chromatin interactions
ENSG00000213159	chromatin interactions

Extended variants
information (count: 3520 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3520 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55779046	chr14:104896538-104896539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576097592	chr14:104896563-104896564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71421300	chr14:104896565-104896566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568748554	chr14:104896590-104896591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374658315	chr14:104896596-104896597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561174239	chr14:104896602-104896603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201290237	chr14:104896620-104896621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112314097	chr14:104896651-104896652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540394735	chr14:104896656-104896657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558917566	chr14:104896697-104896698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560437159	chr14:104896704-104896705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532796940	chr14:104896719-104896720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11851883	chr14:104896748-104896749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372211442	chr14:104896753-104896754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531738295	chr14:104896803-104896804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375931615	chr14:104896815-104896816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568529524	chr14:104896817-104896818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202246905	chr14:104896823-104896824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534183294	chr14:104896825-104896826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553751986	chr14:104896831-104896832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533997216	chr14:104896839-104896840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112770035	chr14:104896858-104896859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553960945	chr14:104896863-104896864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116409856	chr14:104896884-104896885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143357719	chr14:104896897-104896898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555933090	chr14:104896924-104896925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373052932	chr14:104896937-104896938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575971021	chr14:104896950-104896951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28424139	chr14:104896972-104896973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535208219	chr14:104896982-104896983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111360653	chr14:104897004-104897005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571782216	chr14:104897055-104897056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540431696	chr14:104897068-104897069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28433217	chr14:104897090-104897091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560274753	chr14:104897096-104897097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555819598	chr14:104897163-104897164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575872749	chr14:104897177-104897178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546475765	chr14:104897178-104897179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562774070	chr14:104897183-104897184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111678793	chr14:104897185-104897186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531743714	chr14:104897196-104897197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112947303	chr14:104897198-104897199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548572717	chr14:104897208-104897209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562164986	chr14:104897247-104897248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527745180	chr14:104897309-104897310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542015219	chr14:104897329-104897330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547652356	chr14:104897335-104897336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11844784	chr14:104897343-104897344	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570622371	chr14:104897349-104897350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146034772	chr14:104897369-104897370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104888800-104902400	Weak transcription	Right Atrium	heart
2	chr14:104891800-104902200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:104892600-104898600	Weak transcription	Spleen	Spleen
4	chr14:104894000-104897800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:104895600-104901200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:104897800-104900400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:104898200-104898800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:104898400-104898600	Enhancers	Ovary	ovary
9	chr14:104898600-104899400	Enhancers	Spleen	Spleen
10	chr14:104898600-104902200	Weak transcription	Ovary	ovary
11	chr14:104898800-104902000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr14:104899400-104901800	Weak transcription	Spleen	Spleen
13	chr14:104900400-104901000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:104900800-104901200	Enhancers	Brain Germinal Matrix	brain
15	chr14:104901000-104902400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:104901200-104901400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:104901200-104902000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:104901200-104902200	Weak transcription	Brain Germinal Matrix	brain
19	chr14:104901200-104904400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr14:104901400-104902200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:104901400-104904800	Enhancers	Lung	lung
22	chr14:104901800-104902000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:104901800-104902200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:104901800-104902400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:104901800-104902400	Enhancers	Pancreas	Pancrea
26	chr14:104901800-104903200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr14:104901800-104904400	Enhancers	Spleen	Spleen
28	chr14:104902000-104902200	Enhancers	Adipose Nuclei	Adipose
29	chr14:104902000-104902200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
30	chr14:104902000-104902200	Enhancers	Stomach Smooth Muscle	stomach
31	chr14:104902000-104902400	Enhancers	Esophagus	oesophagus
32	chr14:104902000-104902600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr14:104902000-104902600	Bivalent Enhancer	Fetal Stomach	stomach
34	chr14:104902000-104902600	Enhancers	Right Ventricle	heart
35	chr14:104902000-104904000	Enhancers	Fetal Muscle Leg	muscle
36	chr14:104902000-104904200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr14:104902200-104902400	Enhancers	Colon Smooth Muscle	Colon
38	chr14:104902200-104902400	Enhancers	Fetal Lung	lung
39	chr14:104902200-104902400	Enhancers	Placenta	Placenta
40	chr14:104902200-104902400	Enhancers	Ovary	ovary
41	chr14:104902200-104902400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
42	chr14:104902200-104902400	Bivalent Enhancer	Stomach Mucosa	stomach
43	chr14:104902200-104902600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr14:104902200-104902600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr14:104902200-104902600	Enhancers	Brain Hippocampus Middle	brain
46	chr14:104902200-104902600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr14:104902200-104902800	Enhancers	Primary hematopoietic stem cells	blood
48	chr14:104902200-104902800	Enhancers	HUVEC	blood vessel
49	chr14:104902200-104903000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:104902200-104903200	Flanking Active TSS	Adipose Nuclei	Adipose

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