Variant report

Variant	nsv901871
Chromosome Location	chr14:46869797-46961322
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	BCLAF1	chr14:46959550-46960028	GM12878	blood:	n/a	n/a
2	CEBPB	chr14:46959438-46959906	H1-hESC	embryonic stem cell:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
3	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
4	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
5	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
6	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr14:46959344-46959844	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
8	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
9	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
10	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
13	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
14	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
16	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
17	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
18	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
19	CTCF	chr14:46959720-46959870	GM12871	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
20	CTCF	chr14:46959720-46959870	GM12873	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
21	CTCF	chr14:46959680-46959830	HMF	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828
22	CTCF	chr14:46959780-46959930	GM12868	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
23	CTCF	chr14:46959700-46959850	GM12864	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
24	CTCF	chr14:46959699-46959924	GM13977	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
25	CTCF	chr14:46959718-46959872	GM13976	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
26	CTCF	chr14:46959538-46960074	MCF-7	breast:	n/a	chr14:46959657-46959664 chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834 chr14:46959936-46959944
27	CTCF	chr14:46959777-46959847	Hela-S3	cervix:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
28	CTCF	chr14:46959760-46959910	HCPEpiC	choroid plexus:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
29	CTCF	chr14:46959740-46959890	GM06990	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
30	CTCF	chr14:46959720-46959870	HRE	kidney:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
31	CTCF	chr14:46959740-46959890	Caco-2	colon:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
32	CTCF	chr14:46959720-46959870	HA-sp	spinal cord:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
33	CTCF	chr14:46959498-46960139	GM12878	blood:	n/a	chr14:46959657-46959664 chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834 chr14:46959936-46959944
34	CTCF	chr14:46959758-46959857	GM10266	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
35	CTCF	chr14:46959720-46959870	HepG2	liver:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
36	CTCF	chr14:46959780-46959930	BE2_C	brain:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
37	CTCF	chr14:46921113-46921356	GM12878	blood:	n/a	n/a
38	CTCF	chr14:46959780-46959930	GM12869	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
39	CTCF	chr14:46959670-46959988	H1-hESC	embryonic stem cell:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834 chr14:46959936-46959944
40	CTCF	chr14:46959740-46959890	GM12866	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
41	CTCF	chr14:46959780-46959930	HA-sp	spinal cord:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
42	CTCF	chr14:46959740-46959890	HBMEC	blood vessel:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
43	CTCF	chr14:46959739-46959899	Pancreas_OC	pancreas:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
44	CTCF	chr14:46959800-46959950	HMF	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834 chr14:46959936-46959944
45	CTCF	chr14:46959740-46959890	HUVEC	blood vessel:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
46	CTCF	chr14:46959780-46959930	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
47	CTCF	chr14:46959735-46959916	LNCaP	prostate:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
48	CTCF	chr14:46959700-46959850	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
49	CTCF	chr14:46959780-46959930	HCT-116	colon:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
50	CTCF	chr14:46959720-46959870	NB4	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	Hela-S3	cervix:	n/a
2	chr14:46874779-46874829	NH-A	brain:	n/a
3	chr14:46874779-46874829	ovcar-3	ovarian:	n/a
4	chr14:46916528-46916578	HRCEpiC	kidney:	n/a
5	chr14:46916528-46916578	HRE	kidney:	n/a
6	chr14:46874779-46874829	PFSK-1	brain:	n/a
7	chr14:46916080-46916130	AG09319	gingival:	n/a
8	chr14:46874779-46874829	PrEC	prostate:	n/a
9	chr14:46916528-46916578	PrEC	prostate:	n/a
10	chr14:46916528-46916578	U87	brain:	n/a
11	chr14:46916528-46916578	AG04450	lung:	fetal
12	chr14:46874779-46874829	SK-N-SH	brain:	n/a
13	chr14:46916080-46916130	PANC-1	pancreas:	n/a
14	chr14:46916528-46916578	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:46916528-46916578	AG04449	skin:	fetal
16	chr14:46916528-46916578	PFSK-1	brain:	n/a
17	chr14:46874779-46874829	SKMC	muscle:	n/a
18	chr14:46874779-46874829	GM12892	blood:	n/a
19	chr14:46916080-46916130	H1-hESC	embryonic stem cell:	embryo
20	chr14:46916080-46916130	HEEpiC	esophagus:	n/a
21	chr14:46916528-46916578	NB4	blood:	n/a
22	chr14:46874779-46874829	ECC-1	luminal epithelium:	n/a
23	chr14:46874779-46874829	HRPEpiC	eye:	n/a
24	chr14:46916080-46916130	ProgFib	skin:	n/a
25	chr14:46874779-46874829	AG09319	gingival:	n/a
26	chr14:46916080-46916130	NHBE	bronchial:	n/a
27	chr14:46874779-46874829	A549	lung:	n/a
28	chr14:46916528-46916578	HCT-116	colon:	n/a
29	chr14:46916528-46916578	PANC-1	pancreas:	n/a
30	chr14:46874779-46874829	ProgFib	skin:	n/a
31	chr14:46874779-46874829	GM19239	blood:	n/a
32	chr14:46916080-46916130	GM12878	blood:	n/a
33	chr14:46916528-46916578	HRPEpiC	eye:	n/a
34	chr14:46874779-46874829	HRE	kidney:	n/a
35	chr14:46916528-46916578	ECC-1	luminal epithelium:	n/a
36	chr14:46874779-46874829	MCF10A-Er-Src	breast:	n/a
37	chr14:46874779-46874829	HMEC	breast:	n/a
38	chr14:46916528-46916578	SK-N-MC	brain:	n/a
39	chr14:46916080-46916130	IMR90	lung:	fetal
40	chr14:46916080-46916130	K562	blood:	n/a
41	chr14:46874779-46874829	SK-N-MC	brain:	n/a
42	chr14:46916528-46916578	T-47D	breast:	n/a
43	chr14:46874779-46874829	HIPEpiC	eye:	n/a
44	chr14:46916528-46916578	RPTEC	kidney:	n/a
45	chr14:46874779-46874829	HCM	heart:	n/a
46	chr14:46916080-46916130	AG04449	skin:	fetal
47	chr14:46916528-46916578	SAEC	small airway:	n/a
48	chr14:46916080-46916130	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:46874779-46874829	AG10803	skin:	n/a
50	chr14:46916528-46916578	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
2	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
2	lnc-FANCM-6	chr14:46959395-46959490	NONHSAT036681
3	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
4	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681
5	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
6	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680
7	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
8	lnc-FANCM-6	chr14:46959395-46959490	ENSG00000258700
9	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
10	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
11	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
12	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700

Variant related genes	Relation type
LINC00871	TF binding region
LINC00871	CpG island

Extended variants
information (count: 1640 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1999618	chr14:46869797-46869798	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148159184	chr14:46869806-46869807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532370143	chr14:46869831-46869832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143996290	chr14:46869872-46869873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35649859	chr14:46869876-46869877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529648484	chr14:46869885-46869886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548214562	chr14:46869914-46869915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567596914	chr14:46869919-46869920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1999617	chr14:46869930-46869931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs188602093	chr14:46869966-46869967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34406077	chr14:46869969-46869970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571477724	chr14:46869970-46869971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114325092	chr14:46869971-46869972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539377595	chr14:46869988-46869989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193167495	chr14:46869991-46869992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs945024	chr14:46870026-46870027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1999616	chr14:46870033-46870034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369904378	chr14:46870185-46870186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536231857	chr14:46870195-46870196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140913501	chr14:46870216-46870217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572738065	chr14:46870217-46870218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs118137323	chr14:46870292-46870293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573064748	chr14:46870350-46870351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542073048	chr14:46870413-46870414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540506998	chr14:46870495-46870496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558895940	chr14:46870552-46870553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185098998	chr14:46870573-46870574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575846267	chr14:46870589-46870590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17671850	chr14:46870608-46870609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs564556245	chr14:46870615-46870616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367800495	chr14:46870625-46870626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12589450	chr14:46870655-46870656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189949470	chr14:46870664-46870665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541444237	chr14:46870744-46870745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559684747	chr14:46870745-46870746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191659102	chr14:46870753-46870754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546841535	chr14:46870786-46870787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571614174	chr14:46870870-46870871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144770560	chr14:46870880-46870881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs57205646	chr14:46870886-46870887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551186502	chr14:46870899-46870900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183759714	chr14:46870913-46870914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28758280	chr14:46870920-46870921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34426834	chr14:46870921-46870922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536718202	chr14:46870925-46870926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150845860	chr14:46870946-46870947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546940669	chr14:46870969-46870970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534195330	chr14:46871000-46871001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188188673	chr14:46871014-46871015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560645795	chr14:46871032-46871033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46868400-46869800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:46869200-46871000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:46869200-46874200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:46869400-46873000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:46869600-46871800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr14:46869800-46871800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:46869800-46872200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:46870400-46870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr14:46870400-46870600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr14:46870600-46872000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr14:46870800-46872000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr14:46871000-46871600	Enhancers	H9 Cell Line	embryonic stem cell
13	chr14:46871600-46874400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr14:46871800-46872400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr14:46871800-46874200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr14:46871800-46874400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr14:46871800-46875200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr14:46871800-46877200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:46872000-46872200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:46872000-46875000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr14:46872200-46873000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr14:46872200-46877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:46872400-46872800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr14:46872800-46875000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr14:46873000-46873600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr14:46873000-46876200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:46873200-46873600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr14:46873200-46874400	Enhancers	Fetal Lung	lung
29	chr14:46873200-46876000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:46873400-46874200	Enhancers	Fetal Kidney	kidney
31	chr14:46873400-46876000	Enhancers	Brain Germinal Matrix	brain
32	chr14:46873600-46874000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr14:46873600-46874800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr14:46874000-46874200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr14:46874000-46874200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr14:46874200-46874600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:46874200-46874600	Active TSS	Brain Anterior Caudate	brain
38	chr14:46874200-46874600	Enhancers	Placenta Amnion	Placenta Amnion
39	chr14:46874200-46874800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr14:46874200-46874800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr14:46874200-46874800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr14:46874200-46874800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:46874200-46874800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr14:46874200-46874800	Flanking Active TSS	Fetal Kidney	kidney
45	chr14:46874200-46875000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr14:46874200-46875000	Enhancers	Adipose Nuclei	Adipose
47	chr14:46874200-46875000	Enhancers	Brain Substantia Nigra	brain
48	chr14:46874200-46875000	Enhancers	Colon Smooth Muscle	Colon
49	chr14:46874200-46875000	Enhancers	Fetal Intestine Large	intestine
50	chr14:46874200-46875000	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links