Variant report

Variant	esv2758350
Chromosome Location	chr14:26227880-26405118
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:123)
Chromatin interactive
region (count:19)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	CEBPB	chr14:26334939-26335111	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:26392221-26392493	A549	lung:	n/a	chr14:26392336-26392347
4	CEBPB	chr14:26306693-26307062	ECC-1	luminal epithelium:	n/a	chr14:26306901-26306912
5	CEBPB	chr14:26383514-26383723	H1-hESC	embryonic stem cell:	n/a	chr14:26383629-26383640
6	CEBPB	chr14:26273426-26273611	HepG2	liver:	n/a	chr14:26273508-26273519
7	CEBPB	chr14:26294771-26295060	IMR90	lung:	n/a	chr14:26294909-26294920
8	CEBPB	chr14:26383505-26383771	HepG2	liver:	n/a	chr14:26383629-26383640
9	CEBPB	chr14:26301838-26302081	HepG2	liver:	n/a	chr14:26301985-26301996
10	CEBPB	chr14:26398624-26398872	HepG2	liver:	n/a	chr14:26398732-26398743
11	CEBPB	chr14:26392161-26392514	IMR90	lung:	n/a	chr14:26392336-26392347
12	CEBPB	chr14:26294736-26295094	HepG2	liver:	n/a	chr14:26294909-26294920
13	CEBPB	chr14:26378577-26378940	HepG2	liver:	n/a	chr14:26378755-26378766 chr14:26378754-26378765 chr14:26378754-26378767
14	CEBPB	chr14:26392155-26392520	HepG2	liver:	n/a	chr14:26392336-26392347
15	CEBPB	chr14:26296374-26296676	HepG2	liver:	n/a	chr14:26296490-26296501 chr14:26296505-26296516
16	CEBPB	chr14:26378572-26378939	HepG2	liver:	n/a	chr14:26378755-26378766 chr14:26378754-26378765 chr14:26378754-26378767
17	CEBPB	chr14:26272507-26273137	ECC-1	luminal epithelium:	n/a	chr14:26272929-26272942
18	CEBPB	chr14:26301869-26302140	Hela-S3	cervix:	n/a	chr14:26301985-26301996
19	CEBPB	chr14:26378099-26378321	HepG2	liver:	n/a	chr14:26378269-26378280
20	CEBPB	chr14:26378678-26378844	H1-hESC	embryonic stem cell:	n/a	chr14:26378755-26378766 chr14:26378754-26378765 chr14:26378754-26378767
21	CEBPB	chr14:26392174-26392502	H1-hESC	embryonic stem cell:	n/a	chr14:26392336-26392347
22	CEBPB	chr14:26287683-26287884	HepG2	liver:	n/a	chr14:26287770-26287781
23	CEBPB	chr14:26318264-26318435	HepG2	liver:	n/a	chr14:26318356-26318367
24	CEBPB	chr14:26233526-26233660	HepG2	liver:	n/a	chr14:26233592-26233603
25	CEBPB	chr14:26294768-26295028	A549	lung:	n/a	chr14:26294909-26294920
26	CEBPB	chr14:26391142-26391643	HepG2	liver:	n/a	chr14:26391493-26391504
27	CREB1	chr14:26270001-26270407	ECC-1	luminal epithelium:	n/a	n/a
28	CTCF	chr14:26303060-26303210	HRE	kidney:	n/a	chr14:26303117-26303130
29	CTCF	chr14:26365940-26366090	HepG2	liver:	n/a	n/a
30	CTCF	chr14:26302860-26303010	GM06990	blood:	n/a	n/a
31	CTCF	chr14:26303017-26303211	SK-N-SH_RA	brain:	n/a	chr14:26303117-26303130
32	CTCF	chr14:26303019-26303220	MCF-7	breast:	n/a	chr14:26303117-26303130
33	CTCF	chr14:26303060-26303210	HA-sp	spinal cord:	n/a	chr14:26303117-26303130
34	CTCF	chr14:26303040-26303190	HUVEC	blood vessel:	n/a	chr14:26303117-26303130
35	CTCF	chr14:26303020-26303170	BE2_C	brain:	n/a	chr14:26303117-26303130
36	CTCF	chr14:26363068-26363110	GM20000	blood:	n/a	n/a
37	CTCF	chr14:26303080-26303230	SK-N-SH_RA	brain:	n/a	chr14:26303117-26303130
38	CTCF	chr14:26303104-26303205	GM20000	blood:	n/a	chr14:26303117-26303130
39	CTCF	chr14:26303020-26303170	WERI-Rb-1	eye:	n/a	chr14:26303117-26303130
40	CTCF	chr14:26302950-26303248	ECC-1	luminal epithelium:	n/a	chr14:26303117-26303130
41	CTCF	chr14:26303020-26303170	NB4	blood:	n/a	chr14:26303117-26303130
42	CTCF	chr14:26302940-26303090	A549	lung:	n/a	n/a
43	CTCF	chr14:26303060-26303210	SK-N-SH_RA	brain:	n/a	chr14:26303117-26303130
44	CTCF	chr14:26267060-26267210	HepG2	liver:	n/a	n/a
45	CTCF	chr14:26303200-26303350	NHLF	lung:	n/a	n/a
46	CTCF	chr14:26290880-26291030	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:26303020-26303226	MCF-7	breast:	n/a	chr14:26303117-26303130
48	CTCF	chr14:26303089-26303138	Spleen_OC	spleen:	n/a	chr14:26303117-26303130
49	CTCF	chr14:26303020-26303170	HL-60	blood:	n/a	chr14:26303117-26303130
50	CTCF	chr14:26302920-26303070	HCM	heart:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:26338282-26338332	HCPEpiC	choroid plexus:	n/a
2	chr14:26338282-26338332	HCPEpiC	choroid plexus:	n/a
3	chr14:26235384-26235434	AG04450	lung:	fetal
4	chr14:26338282-26338332	NH-A	brain:	n/a
5	chr14:26235384-26235434	AG09319	gingival:	n/a
6	chr14:26235384-26235434	Jurkat	blood:	n/a
7	chr14:26235384-26235434	HIPEpiC	eye:	n/a
8	chr14:26235384-26235434	RPTEC	kidney:	n/a
9	chr14:26235384-26235434	Hepatocyte	liver:	n/a
10	chr14:26235384-26235434	HRPEpiC	eye:	n/a
11	chr14:26235384-26235434	IMR90	lung:	fetal
12	chr14:26235384-26235434	GM12878	blood:	n/a
13	chr14:26338282-26338332	ProgFib	skin:	n/a
14	chr14:26235384-26235434	BE2_C	brain:	n/a
15	chr14:26235384-26235434	GM06990	blood:	n/a
16	chr14:26235384-26235434	ovcar-3	ovarian:	n/a
17	chr14:26235384-26235434	NH-A	brain:	n/a
18	chr14:26338282-26338332	SKMC	muscle:	n/a
19	chr14:26235384-26235434	MCF10A-Er-Src	breast:	n/a
20	chr14:26235384-26235434	GM19239	blood:	n/a
21	chr14:26235384-26235434	ECC-1	luminal epithelium:	n/a
22	chr14:26338282-26338332	HEK293	kidney:	embryo
23	chr14:26235384-26235434	GM12891	blood:	n/a
24	chr14:26235384-26235434	HCT-116	colon:	n/a
25	chr14:26235384-26235434	HCM	heart:	n/a
26	chr14:26338282-26338332	CMK	blood:	n/a
27	chr14:26338282-26338332	K562	blood:	n/a
28	chr14:26338282-26338332	Hela-S3	cervix:	n/a
29	chr14:26338282-26338332	GM12891	blood:	n/a
30	chr14:26235384-26235434	AG10803	skin:	n/a
31	chr14:26338282-26338332	AG09309	skin:	n/a
32	chr14:26235384-26235434	K562	blood:	n/a
33	chr14:26338282-26338332	Caco-2	colon:	n/a
34	chr14:26338282-26338332	AoSMC	blood vessel:	n/a
35	chr14:26338282-26338332	GM19239	blood:	n/a
36	chr14:26235384-26235434	SAEC	small airway:	n/a
37	chr14:26338282-26338332	PANC-1	pancreas:	n/a
38	chr14:26235384-26235434	PANC-1	pancreas:	n/a
39	chr14:26235384-26235434	SK-N-SH_RA	brain:	n/a
40	chr14:26235384-26235434	AoSMC	blood vessel:	n/a
41	chr14:26338282-26338332	HNPCEpiC	eye:	n/a
42	chr14:26338282-26338332	HRE	kidney:	n/a
43	chr14:26235384-26235434	LNCaP	prostate:	n/a
44	chr14:26235384-26235434	AG09309	skin:	n/a
45	chr14:26338282-26338332	U87	brain:	n/a
46	chr14:26235384-26235434	AG04449	skin:	fetal
47	chr14:26338282-26338332	PFSK-1	brain:	n/a
48	chr14:26235384-26235434	NB4	blood:	n/a
49	chr14:26338282-26338332	AG09319	gingival:	n/a
50	chr14:26235384-26235434	HL-60	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:26306524..26308913-chr14:26309516..26311330,2	MCF-7	breast:
2	chr14:26346119..26348327-chr14:26353055..26355310,2	MCF-7	breast:
3	chr14:25900815..25901345-chr14:26290449..26290956,2	MCF-7	breast:
4	chr14:25880977..25881528-chr14:26290650..26291377,2	MCF-7	breast:
5	chr14:26258963..26260708-chr14:26263050..26265355,2	MCF-7	breast:
6	chr14:26231879..26232379-chr14:26263595..26264206,2	MCF-7	breast:
7	chr14:25985949..25986642-chr14:26290498..26291389,5	MCF-7	breast:
8	chr14:26302797..26303465-chr14:26596585..26597346,2	MCF-7	breast:
9	chr14:26302394..26303511-chr14:26477174..26478186,4	MCF-7	breast:
10	chr14:26302691..26303607-chr14:26745704..26746596,2	MCF-7	breast:
11	chr14:26351685..26353304-chr14:26353718..26355297,2	MCF-7	breast:
12	chr14:26351685..26353304-chr14:26353718..26355297,2	MCF-7	breast:
13	chr14:26365992..26367933-chr20:45984526..45986047,2	MCF-7	breast:
14	chr14:26231879..26232379-chr14:26263595..26264206,2	MCF-7	breast:
15	chr14:26258963..26260708-chr14:26263050..26265355,2	MCF-7	breast:
16	chr14:26346119..26348327-chr14:26353055..26355310,2	MCF-7	breast:
17	chr14:26075823..26076989-chr14:26290359..26291621,5	MCF-7	breast:
18	chr14:26097917..26098562-chr14:26290432..26291521,3	MCF-7	breast:
19	chr14:26306524..26308913-chr14:26309516..26311330,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOVA1-8	chr14:26314452-26314745	l_948_chr14:26314451-26361234_kidney
2	lnc-NOVA1-5	chr14:26306335-26306417	ENSG00000257986
3	lnc-NOVA1-7	chr14:26377345-26377512	l_950_chr14:26370460-26377508_testes
4	lnc-NOVA1-7	chr14:26380913-26381149	l_950_chr14:26370460-26377508_testes
5	lnc-NOVA1-7	chr14:26382212-26382350	l_950_chr14:26370460-26377508_testes
6	lnc-RP11-80A15.1.1-10	chr14:26289572-26291947	NONHSAT036086
7	lnc-NOVA1-5	chr14:26305064-26305180	ENSG00000257986
8	lnc-NOVA1-7	chr14:26381611-26381759	l_950_chr14:26370460-26377508_testes
9	lnc-NOVA1-5	chr14:26307666-26307736	ENSG00000257986
10	lnc-NOVA1-7	chr14:26370461-26370590	l_950_chr14:26370460-26377508_testes
11	lnc-RP11-80A15.1.1-11	chr14:26351279-26351442	l_949_chr14:26348362-26366912_testes
12	lnc-NOVA1-8	chr14:26361050-26361234	l_948_chr14:26314451-26361234_kidney
13	lnc-NOVA1-8	chr14:26359738-26359836	l_948_chr14:26314451-26361234_kidney
14	lnc-RP11-80A15.1.1-11	chr14:26348363-26348486	l_949_chr14:26348362-26366912_testes
15	lnc-RP11-80A15.1.1-11	chr14:26366763-26366912	l_949_chr14:26348362-26366912_testes

No data

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

Extended variants
information (count: 5548 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5548 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552536312	chr14:26227881-26227882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572763998	chr14:26227991-26227992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148567707	chr14:26227992-26227993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564949524	chr14:26228001-26228002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530532679	chr14:26228087-26228088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543988216	chr14:26228124-26228125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190711521	chr14:26228177-26228178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200469196	chr14:26228180-26228181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529588875	chr14:26228190-26228191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546365300	chr14:26228226-26228227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142871074	chr14:26228233-26228234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539718664	chr14:26228260-26228261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566389245	chr14:26228274-26228275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150652402	chr14:26228292-26228293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76016871	chr14:26228302-26228303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17110357	chr14:26228317-26228318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs537188588	chr14:26228351-26228352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556717200	chr14:26228445-26228446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540461974	chr14:26228492-26228493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113937177	chr14:26228623-26228624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567158994	chr14:26228638-26228639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140082588	chr14:26228735-26228736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552820310	chr14:26228769-26228770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28684547	chr14:26228775-26228776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544951043	chr14:26228776-26228777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143539031	chr14:26228804-26228805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575296580	chr14:26228824-26228825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555616286	chr14:26228837-26228838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573737425	chr14:26228861-26228862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544350041	chr14:26228868-26228869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563855541	chr14:26228885-26228886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529472282	chr14:26228892-26228893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375709491	chr14:26228959-26228960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560040718	chr14:26229027-26229028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528790431	chr14:26229159-26229160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551741945	chr14:26229169-26229170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571597781	chr14:26229242-26229243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74949086	chr14:26229249-26229250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550628262	chr14:26229258-26229259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543974278	chr14:26229285-26229286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567443513	chr14:26229332-26229333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535995487	chr14:26229338-26229339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377523221	chr14:26229351-26229352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146794082	chr14:26229360-26229361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80105385	chr14:26229372-26229373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538605198	chr14:26229392-26229393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558505200	chr14:26229439-26229440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76384153	chr14:26229486-26229487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537853661	chr14:26229524-26229525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182007942	chr14:26229562-26229563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:26226000-26229000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:26227000-26235600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:26227200-26229200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr14:26227200-26235400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:26227400-26228600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:26227400-26228800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:26228600-26229200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:26228600-26230000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr14:26228600-26230000	Enhancers	Adipose Nuclei	Adipose
10	chr14:26228800-26229000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr14:26228800-26229200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr14:26228800-26230600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:26229000-26229200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr14:26229000-26229600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:26229200-26229400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:26229400-26229800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:26229600-26230200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:26235200-26235800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:26235200-26235800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr14:26235200-26236000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:26235200-26236000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr14:26235200-26236000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr14:26235400-26235800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr14:26235400-26236000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:26235400-26236000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:26235400-26236000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr14:26235600-26236000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:26236000-26236800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr14:26236000-26237400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:26236800-26238400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:26237400-26238200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:26245600-26246200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:26246200-26247400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr14:26246200-26247400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr14:26246400-26246600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr14:26246400-26246600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
37	chr14:26253600-26254000	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr14:26253600-26254000	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr14:26254000-26254200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:26254200-26258400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:26258400-26261400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:26261400-26296400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:26263800-26264000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:26264000-26264200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:26265000-26265400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr14:26265200-26265600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr14:26265200-26265600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr14:26282600-26283200	Enhancers	Brain Angular Gyrus	brain
49	chr14:26282600-26283200	Enhancers	Brain Substantia Nigra	brain
50	chr14:26282800-26283200	Active TSS	Brain Cingulate Gyrus	brain

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