Variant report

Variant	nsv427937
Chromosome Location	chr14:26038386-26405118
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:26296709-26296876	K562	blood:	n/a	n/a
2	BACH1	chr14:26226060-26226404	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:26071333-26071671	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:26167330-26167699	IMR90	lung:	n/a	chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167518 chr14:26167507-26167518 chr14:26167509-26167518 chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167520
5	CEBPB	chr14:26383505-26383771	HepG2	liver:	n/a	chr14:26383629-26383640
6	CEBPB	chr14:26042153-26042154	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:26318264-26318435	HepG2	liver:	n/a	chr14:26318356-26318367
8	CEBPB	chr14:26233526-26233660	HepG2	liver:	n/a	chr14:26233592-26233603
9	CEBPB	chr14:26093310-26093598	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:26301838-26302081	HepG2	liver:	n/a	chr14:26301985-26301996
11	CEBPB	chr14:26227357-26227675	HepG2	liver:	n/a	chr14:26227509-26227520
12	CEBPB	chr14:26378572-26378939	HepG2	liver:	n/a	chr14:26378755-26378766 chr14:26378754-26378765 chr14:26378754-26378767
13	CEBPB	chr14:26151403-26151683	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:26227375-26227571	H1-hESC	embryonic stem cell:	n/a	chr14:26227509-26227520
15	CEBPB	chr14:26095951-26096229	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:26167326-26167696	HepG2	liver:	n/a	chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167518 chr14:26167507-26167518 chr14:26167509-26167518 chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167520
17	CEBPB	chr14:26048971-26049309	HepG2	liver:	n/a	chr14:26049131-26049144 chr14:26049131-26049142
18	CEBPB	chr14:26163596-26163690	A549	lung:	n/a	n/a
19	CEBPB	chr14:26167331-26167669	H1-hESC	embryonic stem cell:	n/a	chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167518 chr14:26167507-26167518 chr14:26167509-26167518 chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167520
20	CEBPB	chr14:26378099-26378321	HepG2	liver:	n/a	chr14:26378269-26378280
21	CEBPB	chr14:26272507-26273137	ECC-1	luminal epithelium:	n/a	chr14:26272929-26272942
22	CEBPB	chr14:26383514-26383723	H1-hESC	embryonic stem cell:	n/a	chr14:26383629-26383640
23	CEBPB	chr14:26167324-26167697	K562	blood:	n/a	chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167518 chr14:26167507-26167518 chr14:26167509-26167518 chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167520
24	CEBPB	chr14:26392221-26392493	A549	lung:	n/a	chr14:26392336-26392347
25	CEBPB	chr14:26132171-26132446	HepG2	liver:	n/a	chr14:26132331-26132344
26	CEBPB	chr14:26167337-26167680	A549	lung:	n/a	chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167518 chr14:26167507-26167518 chr14:26167509-26167518 chr14:26167507-26167520 chr14:26167509-26167518 chr14:26167509-26167520
27	CEBPB	chr14:26113505-26113764	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:26042064-26042397	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:26296374-26296676	HepG2	liver:	n/a	chr14:26296490-26296501 chr14:26296505-26296516
30	CEBPB	chr14:26287683-26287884	HepG2	liver:	n/a	chr14:26287770-26287781
31	CEBPB	chr14:26392155-26392520	HepG2	liver:	n/a	chr14:26392336-26392347
32	CEBPB	chr14:26294736-26295094	HepG2	liver:	n/a	chr14:26294909-26294920
33	CEBPB	chr14:26294768-26295028	A549	lung:	n/a	chr14:26294909-26294920
34	CEBPB	chr14:26273426-26273611	HepG2	liver:	n/a	chr14:26273508-26273519
35	CEBPB	chr14:26073412-26073713	HepG2	liver:	n/a	chr14:26073540-26073551
36	CEBPB	chr14:26226103-26226424	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:26202789-26203091	IMR90	lung:	n/a	chr14:26202921-26202932
38	CEBPB	chr14:26044176-26044397	HepG2	liver:	n/a	chr14:26044252-26044263 chr14:26044254-26044263
39	CEBPB	chr14:26306693-26307062	ECC-1	luminal epithelium:	n/a	chr14:26306901-26306912
40	CEBPB	chr14:26392161-26392514	IMR90	lung:	n/a	chr14:26392336-26392347
41	CEBPB	chr14:26049045-26049251	A549	lung:	n/a	chr14:26049131-26049144 chr14:26049131-26049142
42	CEBPB	chr14:26045692-26045921	HepG2	liver:	n/a	chr14:26045827-26045838
43	CEBPB	chr14:26334939-26335111	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:26202760-26203079	HepG2	liver:	n/a	chr14:26202921-26202932
45	CEBPB	chr14:26391142-26391643	HepG2	liver:	n/a	chr14:26391493-26391504
46	CEBPB	chr14:26398624-26398872	HepG2	liver:	n/a	chr14:26398732-26398743
47	CEBPB	chr14:26378577-26378940	HepG2	liver:	n/a	chr14:26378755-26378766 chr14:26378754-26378765 chr14:26378754-26378767
48	CEBPB	chr14:26049001-26049283	IMR90	lung:	n/a	chr14:26049131-26049144 chr14:26049131-26049142
49	CEBPB	chr14:26294771-26295060	IMR90	lung:	n/a	chr14:26294909-26294920
50	CEBPB	chr14:26301869-26302140	Hela-S3	cervix:	n/a	chr14:26301985-26301996

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:26076574-26076624	Hepatocyte	liver:	n/a
2	chr14:26076574-26076624	Hepatocyte	liver:	n/a
3	chr14:26338282-26338332	AG10803	skin:	n/a
4	chr14:26235384-26235434	SK-N-SH_RA	brain:	n/a
5	chr14:26338282-26338332	GM12891	blood:	n/a
6	chr14:26076574-26076624	SK-N-SH_RA	brain:	n/a
7	chr14:26235384-26235434	AG09309	skin:	n/a
8	chr14:26076574-26076624	A549	lung:	n/a
9	chr14:26076574-26076624	HCM	heart:	n/a
10	chr14:26076574-26076624	PANC-1	pancreas:	n/a
11	chr14:26338282-26338332	AG04449	skin:	fetal
12	chr14:26235384-26235434	HCT-116	colon:	n/a
13	chr14:26076574-26076624	HepG2	liver:	n/a
14	chr14:26076574-26076624	GM12891	blood:	n/a
15	chr14:26226996-26227046	SK-N-SH	brain:	n/a
16	chr14:26226996-26227046	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:26076574-26076624	AG04449	skin:	fetal
18	chr14:26226996-26227046	HL-60	blood:	n/a
19	chr14:26226996-26227046	NB4	blood:	n/a
20	chr14:26226996-26227046	K562	blood:	n/a
21	chr14:26338282-26338332	HRPEpiC	eye:	n/a
22	chr14:26338282-26338332	HMEC	breast:	n/a
23	chr14:26226996-26227046	HCF	heart:	n/a
24	chr14:26076574-26076624	HL-60	blood:	n/a
25	chr14:26235384-26235434	HAEpiC	amniotic membrane:	n/a
26	chr14:26226996-26227046	NT2-D1	testis:	n/a
27	chr14:26338282-26338332	SAEC	small airway:	n/a
28	chr14:26226996-26227046	SKMC	muscle:	n/a
29	chr14:26076574-26076624	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:26226996-26227046	Hela-S3	cervix:	n/a
31	chr14:26226996-26227046	HCM	heart:	n/a
32	chr14:26076574-26076624	HRE	kidney:	n/a
33	chr14:26235384-26235434	ECC-1	luminal epithelium:	n/a
34	chr14:26235384-26235434	ProgFib	skin:	n/a
35	chr14:26076574-26076624	HEEpiC	esophagus:	n/a
36	chr14:26235384-26235434	T-47D	breast:	n/a
37	chr14:26226996-26227046	NHBE	bronchial:	n/a
38	chr14:26338282-26338332	HepG2	liver:	n/a
39	chr14:26235384-26235434	NB4	blood:	n/a
40	chr14:26076574-26076624	IMR90	lung:	fetal
41	chr14:26338282-26338332	BJ	skin:	n/a
42	chr14:26076574-26076624	GM12892	blood:	n/a
43	chr14:26338282-26338332	GM06990	blood:	n/a
44	chr14:26235384-26235434	AG10803	skin:	n/a
45	chr14:26226996-26227046	ovcar-3	ovarian:	n/a
46	chr14:26235384-26235434	IMR90	lung:	fetal
47	chr14:26338282-26338332	ECC-1	luminal epithelium:	n/a
48	chr14:26076574-26076624	SKMC	muscle:	n/a
49	chr14:26226996-26227046	ProgFib	skin:	n/a
50	chr14:26076574-26076624	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:26302691..26303607-chr14:26745704..26746596,2	MCF-7	breast:
2	chr14:26306524..26308913-chr14:26309516..26311330,2	MCF-7	breast:
3	chr14:26258963..26260708-chr14:26263050..26265355,2	MCF-7	breast:
4	chr14:26094691..26096639-chr14:26155868..26157648,2	MCF-7	breast:
5	chr14:26302797..26303465-chr14:26596585..26597346,2	MCF-7	breast:
6	chr14:26346119..26348327-chr14:26353055..26355310,2	MCF-7	breast:
7	chr14:26065183..26067285-chr14:26083351..26085896,2	K562	blood:
8	chr14:26065959..26067623-chr14:26068339..26070541,2	MCF-7	breast:
9	chr14:26346119..26348327-chr14:26353055..26355310,2	MCF-7	breast:
10	chr14:26170940..26172577-chr14:26176461..26179420,2	MCF-7	breast:
11	chr14:26365992..26367933-chr20:45984526..45986047,2	MCF-7	breast:
12	chr14:25926612..25928174-chr14:26066297..26068979,2	MCF-7	breast:
13	chr14:26351685..26353304-chr14:26353718..26355297,2	MCF-7	breast:
14	chr14:26306524..26308913-chr14:26309516..26311330,2	MCF-7	breast:
15	chr14:26170940..26172577-chr14:26176461..26179420,2	MCF-7	breast:
16	chr14:25880977..25881528-chr14:26290650..26291377,2	MCF-7	breast:
17	chr14:26231879..26232379-chr14:26263595..26264206,2	MCF-7	breast:
18	chr14:26075823..26076989-chr14:26290359..26291621,5	MCF-7	breast:
19	chr14:26097917..26098562-chr14:26290432..26291521,3	MCF-7	breast:
20	chr14:26097917..26098562-chr14:26290432..26291521,3	MCF-7	breast:
21	chr14:26258963..26260708-chr14:26263050..26265355,2	MCF-7	breast:
22	chr14:26302394..26303511-chr14:26477174..26478186,4	MCF-7	breast:
23	chr14:26075823..26076989-chr14:26290359..26291621,5	MCF-7	breast:
24	chr14:26065183..26067285-chr14:26083351..26085896,2	K562	blood:
25	chr14:26351685..26353304-chr14:26353718..26355297,2	MCF-7	breast:
26	chr14:26065959..26067623-chr14:26068339..26070541,2	MCF-7	breast:
27	chr14:25900815..25901345-chr14:26290449..26290956,2	MCF-7	breast:
28	chr14:26231879..26232379-chr14:26263595..26264206,2	MCF-7	breast:
29	chr14:25985949..25986642-chr14:26290498..26291389,5	MCF-7	breast:
30	chr14:26094691..26096639-chr14:26155868..26157648,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOVA1-8	chr14:26361050-26361234	l_948_chr14:26314451-26361234_kidney
2	lnc-RP11-80A15.1.1-9	chr14:26203086-26203512	l_947_chr14:26137450-26203512_testes
3	lnc-RP11-80A15.1.1-10	chr14:26289572-26291947	NONHSAT036086
4	lnc-NOVA1-7	chr14:26370461-26370590	l_950_chr14:26370460-26377508_testes
5	lnc-RP11-80A15.1.1-11	chr14:26351279-26351442	l_949_chr14:26348362-26366912_testes
6	lnc-NOVA1-8	chr14:26314452-26314745	l_948_chr14:26314451-26361234_kidney
7	lnc-NOVA1-5	chr14:26305064-26305180	ENSG00000257986
8	lnc-RP11-80A15.1.1-9	chr14:26176241-26176379	l_947_chr14:26137450-26203512_testes
9	lnc-RP11-80A15.1.1-9	chr14:26137451-26137602	l_947_chr14:26137450-26203512_testes
10	lnc-RP11-80A15.1.1-9	chr14:26138291-26139233	l_947_chr14:26137450-26203512_testes
11	lnc-NOVA1-7	chr14:26382212-26382350	l_950_chr14:26370460-26377508_testes
12	lnc-RP11-80A15.1.1-11	chr14:26366763-26366912	l_949_chr14:26348362-26366912_testes
13	lnc-NOVA1-7	chr14:26380913-26381149	l_950_chr14:26370460-26377508_testes
14	lnc-NOVA1-7	chr14:26377345-26377512	l_950_chr14:26370460-26377508_testes
15	lnc-NOVA1-8	chr14:26359738-26359836	l_948_chr14:26314451-26361234_kidney
16	lnc-RP11-80A15.1.1-11	chr14:26348363-26348486	l_949_chr14:26348362-26366912_testes
17	lnc-NOVA1-5	chr14:26307666-26307736	ENSG00000257986
18	lnc-NOVA1-5	chr14:26306335-26306417	ENSG00000257986
19	lnc-NOVA1-7	chr14:26381611-26381759	l_950_chr14:26370460-26377508_testes
20	lnc-RP11-80A15.1.1-9	chr14:26202659-26202976	l_947_chr14:26137450-26203512_testes
21	lnc-RP11-80A15.1.1-9	chr14:26186031-26186125	l_947_chr14:26137450-26203512_testes
22	lnc-RP11-80A15.1.1-9	chr14:26162250-26162371	l_947_chr14:26137450-26203512_testes

Variant related genes	Relation type
ENSG00000212270	TF binding region
ENSG00000212270	CpG island
ENSG00000101040	chromatin interactions

Extended variants
information (count: 7821 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:7821 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556088737	chr14:26044873-26044874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560779512	chr14:26044886-26044887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577611141	chr14:26044924-26044925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182189150	chr14:26044940-26044941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35675501	chr14:26044962-26044963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546548147	chr14:26045058-26045059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562855660	chr14:26045073-26045074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531759471	chr14:26045103-26045104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577627315	chr14:26045106-26045107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs926912	chr14:26045124-26045125	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs562049784	chr14:26045144-26045145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527825228	chr14:26045146-26045147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547270011	chr14:26045177-26045178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140561701	chr14:26045189-26045190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540662597	chr14:26045190-26045191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76254475	chr14:26045247-26045248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527262009	chr14:26045268-26045269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187911622	chr14:26045289-26045290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535086854	chr14:26045292-26045293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192527912	chr14:26045310-26045311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542684130	chr14:26045316-26045317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs926911	chr14:26045320-26045321	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs183064696	chr14:26045353-26045354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532044124	chr14:26045365-26045366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112330583	chr14:26045385-26045386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550354734	chr14:26045448-26045449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112294869	chr14:26045676-26045677	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs373648783	chr14:26045735-26045736	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs546486738	chr14:26045752-26045753	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559757102	chr14:26045803-26045804	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs1951072	chr14:26045840-26045841	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145672790	chr14:26045849-26045850	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541848522	chr14:26045859-26045860	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs562157935	chr14:26045865-26045866	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532606795	chr14:26045875-26045876	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs527760083	chr14:26045922-26045923	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs541547426	chr14:26045936-26045937	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs188736098	chr14:26045963-26045964	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs547554347	chr14:26045985-26045986	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs549620228	chr14:26046003-26046004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146587313	chr14:26046054-26046055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529193645	chr14:26046058-26046059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141193206	chr14:26046101-26046102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113374298	chr14:26046166-26046167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12882376	chr14:26046177-26046178	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs192829178	chr14:26046182-26046183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185033042	chr14:26046207-26046208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571009723	chr14:26046211-26046212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187903542	chr14:26046227-26046228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72692222	chr14:26046242-26046243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:26044800-26046600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:26045000-26045600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr14:26045000-26046600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:26045200-26046200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr14:26045200-26046600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:26045400-26046400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr14:26045400-26046400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:26045600-26046000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr14:26045600-26046600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr14:26046000-26046600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr14:26055400-26055600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:26055600-26061400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:26073000-26073200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:26075200-26076800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:26075800-26076200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr14:26075800-26076400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr14:26075800-26077000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr14:26076000-26076800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr14:26076000-26076800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr14:26076000-26076800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr14:26076000-26077000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr14:26076000-26077200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr14:26076000-26077200	Enhancers	Brain Substantia Nigra	brain
24	chr14:26076000-26077400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:26076000-26077800	Enhancers	Brain Hippocampus Middle	brain
26	chr14:26076000-26078400	Enhancers	Brain Cingulate Gyrus	brain
27	chr14:26076200-26077200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr14:26076400-26076600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr14:26076400-26076600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:26076400-26076800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr14:26076600-26076800	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr14:26076600-26076800	Enhancers	Fetal Lung	lung
33	chr14:26076800-26077000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr14:26076800-26077200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr14:26077000-26077200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr14:26077200-26077400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr14:26077200-26077600	Weak transcription	Brain Substantia Nigra	brain
38	chr14:26077600-26078000	Enhancers	Brain Substantia Nigra	brain
39	chr14:26085800-26086600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr14:26086200-26086600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:26086200-26086600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr14:26086200-26086600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:26086600-26099400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:26092000-26092400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr14:26095800-26096000	Enhancers	Fetal Kidney	kidney
46	chr14:26095800-26096600	Enhancers	Fetal Stomach	stomach
47	chr14:26096400-26097800	Weak transcription	Fetal Kidney	kidney
48	chr14:26096600-26098600	Weak transcription	Fetal Stomach	stomach
49	chr14:26097400-26099400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr14:26097800-26098600	Enhancers	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links