Variant report

Variant	nsv519840
Chromosome Location	chr14:104884605-104961635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:328)
CpG islands
(count:2258)
Chromatin interactive
region (count:31)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:104910308-104910836	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	chr14:104927523-104927809	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr14:104937869-104938923	GM12878	blood:	n/a	n/a
5	BCL3	chr14:104906905-104907311	GM12878	blood:	n/a	n/a
6	BCL3	chr14:104910462-104910720	GM12878	blood:	n/a	n/a
7	BCL3	chr14:104910404-104910832	GM12878	blood:	n/a	n/a
8	BCL3	chr14:104937880-104938837	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104906971-104907201	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:104891140-104891268	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:104891142-104891342	K562	blood:	n/a	n/a
12	CBX3	chr14:104948502-104948667	K562	blood:	n/a	n/a
13	CEBPB	chr14:104929365-104929595	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:104961481-104961670	A549	lung:	n/a	n/a
15	CEBPB	chr14:104954841-104955082	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:104929360-104929668	A549	lung:	n/a	n/a
17	CEBPB	chr14:104929383-104929624	IMR90	lung:	n/a	n/a
18	CEBPB	chr14:104927611-104927725	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr14:104909120-104909319	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr14:104886256-104886838	GM12878	blood:	n/a	n/a
21	CREB1	chr14:104943728-104944011	A549	lung:	n/a	n/a
22	CREB1	chr14:104886313-104886828	GM12878	blood:	n/a	n/a
23	CTCF	chr14:104920787-104920790	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:104939660-104939810	WERI-Rb-1	eye:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
25	CTCF	chr14:104953632-104953753	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:104909900-104910050	GM12864	blood:	n/a	n/a
27	CTCF	chr14:104909880-104910030	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr14:104939620-104939770	HUVEC	blood vessel:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
29	CTCF	chr14:104953611-104953784	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:104917600-104917750	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr14:104894625-104894671	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr14:104902369-104902416	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr14:104900260-104900410	GM12870	blood:	n/a	chr14:104900373-104900391
34	CTCF	chr14:104902260-104902410	HepG2	liver:	n/a	n/a
35	CTCF	chr14:104920710-104920785	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:104920692-104920737	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr14:104900217-104900529	GM12878	blood:	n/a	chr14:104900373-104900391
38	CTCF	chr14:104909932-104909972	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:104902280-104902430	BE2_C	brain:	n/a	n/a
40	CTCF	chr14:104939640-104939790	WERI-Rb-1	eye:	n/a	chr14:104939691-104939709 chr14:104939686-104939707 chr14:104939693-104939706
41	CTCF	chr14:104909420-104909570	GM12864	blood:	n/a	n/a
42	CTCF	chr14:104953580-104953730	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:104902220-104902370	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr14:104940200-104940350	GM06990	blood:	n/a	chr14:104940244-104940257
45	CTCF	chr14:104953619-104953786	LNCaP	prostate:	n/a	n/a
46	CTCF	chr14:104909860-104910010	GM12871	blood:	n/a	n/a
47	CTCF	chr14:104953620-104953770	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:104900344-104900435	GM12878	blood:	n/a	chr14:104900373-104900391
49	CTCF	chr14:104909842-104910100	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr14:104900288-104900295	Lung_OC	lung:	n/a	n/a

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104925368-104925418	NB4	blood:	n/a
2	chr14:104925368-104925418	NB4	blood:	n/a
3	chr14:104896560-104896610	NB4	blood:	n/a
4	chr14:104889116-104889166	Jurkat	blood:	n/a
5	chr14:104937088-104937138	AG10803	skin:	n/a
6	chr14:104893636-104893686	GM12892	blood:	n/a
7	chr14:104889116-104889166	SKMC	muscle:	n/a
8	chr14:104940465-104940515	HRE	kidney:	n/a
9	chr14:104928675-104928725	PANC-1	pancreas:	n/a
10	chr14:104937088-104937138	GM19239	blood:	n/a
11	chr14:104888911-104888961	PrEC	prostate:	n/a
12	chr14:104898358-104898408	Hela-S3	cervix:	n/a
13	chr14:104889116-104889166	SAEC	small airway:	n/a
14	chr14:104917157-104917207	HMEC	breast:	n/a
15	chr14:104940369-104940419	BE2_C	brain:	n/a
16	chr14:104896758-104896808	HUVEC	blood vessel:	n/a
17	chr14:104917157-104917207	NHBE	bronchial:	n/a
18	chr14:104927127-104927177	A549	lung:	n/a
19	chr14:104897608-104897658	Hepatocyte	liver:	n/a
20	chr14:104889005-104889055	HCM	heart:	n/a
21	chr14:104940658-104940708	HNPCEpiC	eye:	n/a
22	chr14:104940939-104940989	Hela-S3	cervix:	n/a
23	chr14:104931470-104931520	AG09319	gingival:	n/a
24	chr14:104941923-104941973	HIPEpiC	eye:	n/a
25	chr14:104909505-104909555	GM12892	blood:	n/a
26	chr14:104928472-104928522	SK-N-SH	brain:	n/a
27	chr14:104928675-104928725	GM12891	blood:	n/a
28	chr14:104940386-104940436	AG04450	lung:	fetal
29	chr14:104937088-104937138	ProgFib	skin:	n/a
30	chr14:104940386-104940436	CMK	blood:	n/a
31	chr14:104896758-104896808	Hepatocyte	liver:	n/a
32	chr14:104940386-104940436	SK-N-SH_RA	brain:	n/a
33	chr14:104896001-104896051	T-47D	breast:	n/a
34	chr14:104888911-104888961	CMK	blood:	n/a
35	chr14:104896090-104896140	MCF-7	breast:	n/a
36	chr14:104896758-104896808	HRCEpiC	kidney:	n/a
37	chr14:104897068-104897118	HAEpiC	amniotic membrane:	n/a
38	chr14:104898358-104898408	HNPCEpiC	eye:	n/a
39	chr14:104902678-104902728	ovcar-3	ovarian:	n/a
40	chr14:104888911-104888961	Jurkat	blood:	n/a
41	chr14:104896001-104896051	GM06990	blood:	n/a
42	chr14:104896758-104896808	GM12892	blood:	n/a
43	chr14:104944443-104944493	ProgFib	skin:	n/a
44	chr14:104940658-104940708	T-47D	breast:	n/a
45	chr14:104900453-104900503	GM12878	blood:	n/a
46	chr14:104889005-104889055	HEK293	kidney:	embryo
47	chr14:104917314-104917364	ProgFib	skin:	n/a
48	chr14:104928472-104928522	Hela-S3	cervix:	n/a
49	chr14:104928675-104928725	HAEpiC	amniotic membrane:	n/a
50	chr14:104898358-104898408	HCF	heart:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
2	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
3	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
4	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
5	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
6	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
7	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
8	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
9	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
10	chr14:104940339..104943047-chr14:104952341..104955339,2	MCF-7	breast:
11	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
12	chr14:104898141..104899816-chr14:104900937..104903488,2	MCF-7	breast:
13	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
14	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
15	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
16	chr14:104913762..104916000-chr14:104927543..104930360,2	MCF-7	breast:
17	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
18	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
19	chr14:104926023..104927806-chr14:104944745..104946610,2	MCF-7	breast:
20	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
21	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
22	chr14:104907745..104909314-chr14:105070369..105072440,2	MCF-7	breast:
23	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
24	chr14:104935381..104936897-chr14:104942473..104945422,2	MCF-7	breast:
25	chr14:104940339..104943047-chr14:104952341..104955339,2	MCF-7	breast:
26	chr14:104936926..104938597-chr14:104940514..104942466,3	MCF-7	breast:
27	chr14:104907597..104909438-chr14:105077013..105079589,2	K562	blood:
28	chr14:104917302..104919822-chr14:104924215..104925879,2	K562	blood:
29	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
30	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
31	chr14:104915992..104918653-chr14:104925232..104927798,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3286 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3286 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563715059	chr14:104885030-104885031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186670652	chr14:104885075-104885076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549531541	chr14:104885096-104885097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540140818	chr14:104885097-104885098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73352147	chr14:104885115-104885116	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551288006	chr14:104885128-104885129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571376781	chr14:104885176-104885177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548195008	chr14:104885208-104885209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191182697	chr14:104885212-104885213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183121334	chr14:104885220-104885221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188548339	chr14:104885231-104885232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373541252	chr14:104885241-104885242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4310788	chr14:104885264-104885265	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs35690337	chr14:104885280-104885281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193153711	chr14:104885285-104885286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141553549	chr14:104885324-104885325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558077536	chr14:104885338-104885339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578211601	chr14:104885544-104885545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544617044	chr14:104885557-104885558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184806859	chr14:104885558-104885559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572113591	chr14:104885609-104885610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563955743	chr14:104885651-104885652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187707713	chr14:104885652-104885653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115520656	chr14:104885689-104885690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs8009494	chr14:104885716-104885717	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs567005343	chr14:104885728-104885729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192364138	chr14:104885734-104885735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577731164	chr14:104885749-104885750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543775211	chr14:104885773-104885774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116343990	chr14:104885784-104885785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571397484	chr14:104885860-104885861	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs563554566	chr14:104885924-104885925	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs550497703	chr14:104886006-104886007	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145335724	chr14:104886007-104886008	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373484798	chr14:104886032-104886033	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536115666	chr14:104886163-104886164	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552698413	chr14:104886174-104886175	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs75577107	chr14:104886211-104886212	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538396747	chr14:104886271-104886272	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs183696061	chr14:104886292-104886293	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs578233242	chr14:104886299-104886300	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs149121136	chr14:104886354-104886355	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs76312979	chr14:104886425-104886426	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs574388208	chr14:104886439-104886440	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs189271196	chr14:104886454-104886455	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs370569217	chr14:104886456-104886457	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs559525530	chr14:104886457-104886458	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181433580	chr14:104886500-104886501	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs550808153	chr14:104886509-104886510	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545196783	chr14:104886530-104886531	Enhancers Weak transcription Flanking Active TSS	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:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104885000-104885600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:104885200-104885600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:104885200-104885800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr14:104885400-104885800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:104885400-104886400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr14:104885600-104886600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr14:104885800-104886200	Active TSS	Brain Germinal Matrix	brain
8	chr14:104885800-104886200	Enhancers	GM12878-XiMat	blood
9	chr14:104885800-104891200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:104886200-104886600	Flanking Active TSS	Brain Germinal Matrix	brain
11	chr14:104886200-104886800	Flanking Active TSS	GM12878-XiMat	blood
12	chr14:104886200-104887200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:104886200-104887200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr14:104886200-104892800	Enhancers	Fetal Brain Male	brain
15	chr14:104886400-104886800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:104886400-104886800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr14:104886400-104886800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr14:104886600-104886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr14:104886600-104886800	Enhancers	Fetal Muscle Leg	muscle
20	chr14:104886600-104887200	Enhancers	Fetal Lung	lung
21	chr14:104886600-104887200	Enhancers	Ovary	ovary
22	chr14:104886600-104894200	Enhancers	Brain Germinal Matrix	brain
23	chr14:104886800-104887000	Enhancers	Brain Cingulate Gyrus	brain
24	chr14:104886800-104887000	Enhancers	Fetal Stomach	stomach
25	chr14:104886800-104887200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr14:104886800-104887400	Enhancers	Fetal Muscle Trunk	muscle
27	chr14:104886800-104887600	Enhancers	GM12878-XiMat	blood
28	chr14:104886800-104887800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:104886800-104892600	Enhancers	Fetal Brain Female	brain
30	chr14:104887000-104890800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr14:104887200-104888000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:104887200-104888000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:104887200-104890200	Weak transcription	Ovary	ovary
34	chr14:104887200-104890600	Weak transcription	Fetal Lung	lung
35	chr14:104887200-104893200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:104887400-104892600	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr14:104887400-104892800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr14:104887800-104888000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:104887800-104891800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr14:104888000-104888200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr14:104888000-104888600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:104888000-104889400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:104888200-104888800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr14:104888400-104889200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr14:104888400-104889400	Enhancers	Brain Hippocampus Middle	brain
46	chr14:104888400-104889600	Enhancers	Colon Smooth Muscle	Colon
47	chr14:104888400-104892000	Bivalent Enhancer	Fetal Stomach	stomach
48	chr14:104888600-104888800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:104888600-104888800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr14:104888600-104889000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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