Variant report

Variant	nsv1036267
Chromosome Location	chr14:46491828-46804734
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	ATF2	chr14:46791299-46791687	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:46559473-46559585	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:46791333-46791636	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:46791312-46791676	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr14:46517423-46517924	HCT-116	colon:	n/a	n/a
6	CEBPB	chr14:46624367-46624581	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
8	CEBPB	chr14:46624384-46624661	A549	lung:	n/a	n/a
9	CEBPB	chr14:46624371-46624707	IMR90	lung:	n/a	n/a
10	CEBPB	chr14:46791324-46791680	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:46705042-46705302	IMR90	lung:	n/a	n/a
12	CEBPB	chr14:46629938-46630176	A549	lung:	n/a	n/a
13	CEBPB	chr14:46504576-46504826	HepG2	liver:	n/a	chr14:46504676-46504687
14	CEBPB	chr14:46629835-46630166	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:46673638-46673846	HepG2	liver:	n/a	chr14:46673736-46673749 chr14:46673736-46673747 chr14:46673736-46673749
16	CEBPB	chr14:46560063-46560127	K562	blood:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
17	CEBPB	chr14:46504563-46504826	IMR90	lung:	n/a	chr14:46504676-46504687
18	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:46547984-46548190	HepG2	liver:	n/a	chr14:46548062-46548073
20	CEBPB	chr14:46624379-46624686	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr14:46688915-46689127	HepG2	liver:	n/a	chr14:46689036-46689047
22	CEBPB	chr14:46559920-46560194	A549	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
23	CEBPB	chr14:46523694-46524102	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:46559949-46560242	HepG2	liver:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
25	CEBPB	chr14:46587638-46587921	HepG2	liver:	n/a	chr14:46587769-46587780
26	CEBPB	chr14:46559908-46560222	IMR90	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
27	CEBPB	chr14:46688925-46689144	IMR90	lung:	n/a	chr14:46689036-46689047
28	CEBPB	chr14:46504544-46504822	A549	lung:	n/a	chr14:46504676-46504687
29	CEBPB	chr14:46615814-46615966	K562	blood:	n/a	n/a
30	CEBPB	chr14:46732453-46732625	HepG2	liver:	n/a	chr14:46732582-46732593 chr14:46732584-46732593
31	CEBPB	chr14:46669191-46669427	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:46658833-46659107	HepG2	liver:	n/a	chr14:46658963-46658974
33	CHD2	chr14:46791309-46791730	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr14:46791285-46791675	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr14:46719380-46719530	GM12872	blood:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
36	CTCF	chr14:46719306-46719633	K562	blood:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
37	CTCF	chr14:46517460-46517610	HMF	breast:	n/a	n/a
38	CTCF	chr14:46517380-46517530	GM12871	blood:	n/a	n/a
39	CTCF	chr14:46517420-46517570	BE2_C	brain:	n/a	n/a
40	CTCF	chr14:46719380-46719530	HCM	heart:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
41	CTCF	chr14:46503760-46503910	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:46719400-46719559	Kidney_OC	kidney:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
43	CTCF	chr14:46517420-46517570	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr14:46517440-46517590	AG04449	skin:	n/a	n/a
45	CTCF	chr14:46517371-46517628	GM12878	blood:	n/a	n/a
46	CTCF	chr14:46517386-46517678	Fibrobl	skin:	n/a	n/a
47	CTCF	chr14:46719400-46719550	NHEK	skin:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
48	CTCF	chr14:46517480-46517630	RPTEC	kidney:	n/a	n/a
49	CTCF	chr14:46794480-46794630	Caco-2	colon:	n/a	n/a
50	CTCF	chr14:46719300-46719450	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46791389-46791439	GM06990	blood:	n/a
2	chr14:46791389-46791439	NHBE	bronchial:	n/a
3	chr14:46791389-46791439	SK-N-SH_RA	brain:	n/a
4	chr14:46791389-46791439	H1-hESC	embryonic stem cell:	embryo
5	chr14:46791389-46791439	RPTEC	kidney:	n/a
6	chr14:46791389-46791439	HCM	heart:	n/a
7	chr14:46791389-46791439	GM12891	blood:	n/a
8	chr14:46791389-46791439	HCPEpiC	choroid plexus:	n/a
9	chr14:46791389-46791439	Hela-S3	cervix:	n/a
10	chr14:46791389-46791439	HepG2	liver:	n/a
11	chr14:46791389-46791439	SAEC	small airway:	n/a
12	chr14:46791389-46791439	ovcar-3	ovarian:	n/a
13	chr14:46791389-46791439	Caco-2	colon:	n/a
14	chr14:46791389-46791439	NH-A	brain:	n/a
15	chr14:46791389-46791439	T-47D	breast:	n/a
16	chr14:46791389-46791439	AG04450	lung:	fetal
17	chr14:46791389-46791439	ProgFib	skin:	n/a
18	chr14:46791389-46791439	HIPEpiC	eye:	n/a
19	chr14:46791389-46791439	HL-60	blood:	n/a
20	chr14:46791389-46791439	BE2_C	brain:	n/a
21	chr14:46791389-46791439	HEEpiC	esophagus:	n/a
22	chr14:46791389-46791439	Hepatocyte	liver:	n/a
23	chr14:46791389-46791439	HRPEpiC	eye:	n/a
24	chr14:46791389-46791439	GM19239	blood:	n/a
25	chr14:46791389-46791439	MCF-7	breast:	n/a
26	chr14:46791389-46791439	PANC-1	pancreas:	n/a
27	chr14:46791389-46791439	HRE	kidney:	n/a
28	chr14:46791389-46791439	BJ	skin:	n/a
29	chr14:46791389-46791439	SK-N-MC	brain:	n/a
30	chr14:46791389-46791439	SKMC	muscle:	n/a
31	chr14:46791389-46791439	HEK293	kidney:	embryo
32	chr14:46791389-46791439	ECC-1	luminal epithelium:	n/a
33	chr14:46791389-46791439	GM12878	blood:	n/a
34	chr14:46791389-46791439	AG09319	gingival:	n/a
35	chr14:46791389-46791439	HMEC	breast:	n/a
36	chr14:46791389-46791439	K562	blood:	n/a
37	chr14:46791389-46791439	HNPCEpiC	eye:	n/a
38	chr14:46791389-46791439	AG09309	skin:	n/a
39	chr14:46791389-46791439	PrEC	prostate:	n/a
40	chr14:46791389-46791439	AG04449	skin:	fetal
41	chr14:46791389-46791439	A549	lung:	n/a
42	chr14:46791389-46791439	U87	brain:	n/a
43	chr14:46791389-46791439	NHDF-neo	bronchial:	n/a
44	chr14:46791389-46791439	HCT-116	colon:	n/a
45	chr14:46791389-46791439	NT2-D1	testis:	n/a
46	chr14:46791389-46791439	LNCaP	prostate:	n/a
47	chr14:46791389-46791439	CMK	blood:	n/a
48	chr14:46791389-46791439	Jurkat	blood:	n/a
49	chr14:46791389-46791439	AoSMC	blood vessel:	n/a
50	chr14:46791389-46791439	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
2	chr14:46517458..46517985-chr14:47049934..47050581,2	MCF-7	breast:
3	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
4	chr14:46557288..46558270-chr17:53789584..53790485,2	MCF-7	breast:
5	chr14:46538407..46539085-chr4:43195045..43195862,2	MCF-7	breast:
6	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:
7	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
2	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036678
3	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
4	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036678
5	lnc-FANCM-6	chr14:46788016-46788064	ENSG00000258700
6	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036679
7	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700
8	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036679
9	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036678
10	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036679
11	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700
12	lnc-FANCM-6	chr14:46533362-46533419	ENSG00000258700

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

Extended variants
information (count: 2971 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2971 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1570176	chr14:46491828-46491829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142111130	chr14:46491858-46491859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546611443	chr14:46491876-46491877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79538967	chr14:46491894-46491895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1570175	chr14:46491899-46491900	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1570174	chr14:46491905-46491906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549750714	chr14:46491919-46491920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555765593	chr14:46491925-46491926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537603992	chr14:46492000-46492001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569272200	chr14:46492019-46492020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370734264	chr14:46492039-46492040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573983188	chr14:46492044-46492045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17116856	chr14:46492047-46492048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552924801	chr14:46492049-46492050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376916003	chr14:46492072-46492073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529433800	chr14:46492075-46492076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1160792	chr14:46492129-46492130	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571939091	chr14:46492149-46492150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370518884	chr14:46492303-46492304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147199138	chr14:46492329-46492330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370837929	chr14:46492332-46492333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575354161	chr14:46492333-46492334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201552594	chr14:46492361-46492362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542805830	chr14:46492378-46492379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561207943	chr14:46492387-46492388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528380661	chr14:46492413-46492414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373701090	chr14:46492426-46492427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377684260	chr14:46492482-46492483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564889363	chr14:46492500-46492501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534802624	chr14:46492509-46492510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147781197	chr14:46492528-46492529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550406108	chr14:46492559-46492560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77945699	chr14:46492577-46492578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531050974	chr14:46492580-46492581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192808748	chr14:46492614-46492615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs80247817	chr14:46492629-46492630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79165464	chr14:46492636-46492637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141102367	chr14:46492642-46492643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554433038	chr14:46492657-46492658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571319627	chr14:46492668-46492669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147119853	chr14:46492715-46492716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557222918	chr14:46492798-46492799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575684886	chr14:46492816-46492817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542492852	chr14:46492845-46492846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201931231	chr14:46492865-46492866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368275912	chr14:46492867-46492868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574899338	chr14:46492876-46492877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147736716	chr14:46492905-46492906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573047572	chr14:46492923-46492924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186795536	chr14:46492944-46492945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46488200-46492400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr14:46489400-46493000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr14:46492400-46492800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr14:46493000-46493200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:46505000-46505800	Enhancers	NHEK	skin
6	chr14:46509200-46509800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:46516600-46518000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:46516800-46517000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr14:46517000-46517800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:46517000-46517800	Enhancers	NHEK	skin
11	chr14:46517200-46518000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:46517200-46518000	Enhancers	HMEC	breast
13	chr14:46517200-46518400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:46517400-46518000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:46517400-46518000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr14:46517400-46518000	Enhancers	NH-A	brain
17	chr14:46517400-46518200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:46517600-46518000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:46517600-46518000	Enhancers	HUVEC	blood vessel
20	chr14:46517600-46518200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:46517600-46518200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:46517600-46518200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr14:46517600-46518200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:46517600-46518600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr14:46517800-46518200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr14:46517800-46523000	Weak transcription	NHEK	skin
27	chr14:46518000-46521000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr14:46518000-46523000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:46518000-46523000	Weak transcription	HMEC	breast
30	chr14:46518200-46520200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:46518200-46521000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr14:46520200-46521400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:46521000-46521400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr14:46521000-46521400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:46521000-46521600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr14:46521600-46523000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr14:46523000-46524200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr14:46523000-46524200	Enhancers	HMEC	breast
39	chr14:46523000-46524400	Enhancers	NHEK	skin
40	chr14:46523000-46525000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:46523200-46524400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:46523600-46524200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr14:46523600-46524200	Enhancers	NH-A	brain
44	chr14:46523800-46524200	Enhancers	Fetal Brain Female	brain
45	chr14:46524000-46524200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:46524800-46525000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:46527600-46528200	Enhancers	GM12878-XiMat	blood
48	chr14:46528200-46528600	Flanking Active TSS	GM12878-XiMat	blood
49	chr14:46533000-46533600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr14:46560400-46562200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links