Variant report

Variant	nsv524342
Chromosome Location	chr4:55891531-55921535
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	CEBPB	chr4:55904160-55904777	ECC-1	luminal epithelium:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
2	CEBPB	chr4:55919600-55919907	HepG2	liver:	n/a	chr4:55919786-55919797
3	CEBPB	chr4:55904245-55904798	ECC-1	luminal epithelium:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
4	CEBPB	chr4:55904308-55904710	MCF-7	breast:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
5	CEBPB	chr4:55904365-55904663	Hela-S3	cervix:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
6	CEBPB	chr4:55904367-55904648	H1-hESC	embryonic stem cell:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
7	CEBPB	chr4:55904349-55904657	K562	blood:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
8	CEBPB	chr4:55919597-55919887	IMR90	lung:	n/a	chr4:55919786-55919797
9	CEBPB	chr4:55900557-55900780	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:55895720-55895747	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:55904325-55904680	IMR90	lung:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
12	CEBPB	chr4:55904331-55904664	HepG2	liver:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
13	CEBPB	chr4:55904342-55904677	A549	lung:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
14	CEBPB	chr4:55904296-55904661	MCF-7	breast:	n/a	chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904496-55904509 chr4:55904496-55904507 chr4:55904498-55904507 chr4:55904498-55904507 chr4:55904498-55904509 chr4:55904496-55904509
15	CEBPD	chr4:55899919-55900320	K562	blood:	n/a	n/a
16	CHD2	chr4:55919222-55919442	K562	blood:	n/a	n/a
17	CTCF	chr4:55896553-55896588	Lung_OC	lung:	n/a	n/a
18	CTCF	chr4:55891875-55891882	LNCaP	prostate:	n/a	n/a
19	CTCF	chr4:55907920-55908070	GM12873	blood:	n/a	n/a
20	CTCF	chr4:55908929-55909019	Lung_OC	lung:	n/a	n/a
21	EP300	chr4:55904172-55904919	ECC-1	luminal epithelium:	n/a	n/a
22	FOS	chr4:55896957-55897157	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr4:55919680-55919914	MCF10A-Er-Src	breast:	n/a	chr4:55919783-55919795
24	FOS	chr4:55904403-55904837	MCF10A-Er-Src	breast:	n/a	chr4:55904453-55904465
25	FOS	chr4:55904393-55904624	MCF10A-Er-Src	breast:	n/a	chr4:55904453-55904465
26	FOS	chr4:55899525-55899860	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:55904356-55904735	MCF10A-Er-Src	breast:	n/a	chr4:55904453-55904465
28	FOS	chr4:55919600-55919890	MCF10A-Er-Src	breast:	n/a	chr4:55919783-55919795
29	FOS	chr4:55897464-55897674	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:55896948-55897254	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr4:55899560-55899784	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:55899266-55899860	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:55896935-55897234	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:55897569-55897907	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:55903613-55903930	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:55899541-55899824	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:55899018-55899254	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:55904276-55904676	MCF10A-Er-Src	breast:	n/a	chr4:55904453-55904465
39	FOS	chr4:55903606-55903898	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:55919632-55919880	MCF10A-Er-Src	breast:	n/a	chr4:55919783-55919795
41	FOS	chr4:55902115-55902430	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA2	chr4:55907732-55908082	A549	lung:	n/a	n/a
43	GATA2	chr4:55896757-55897105	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr4:55896891-55897155	SH-SY5Y	brain:	n/a	n/a
45	HEY1	chr4:55894981-55895150	HepG2	liver:	n/a	n/a
46	HEY1	chr4:55894902-55895168	K562	blood:	n/a	n/a
47	HEY1	chr4:55894820-55895283	HepG2	liver:	n/a	n/a
48	HEY1	chr4:55894951-55895207	K562	blood:	n/a	n/a
49	IRF1	chr4:55906610-55906654	K562	blood:	n/a	n/a
50	JUND	chr4:55893442-55893592	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55896358-55896408	HCPEpiC	choroid plexus:	n/a
2	chr4:55896358-55896408	Hela-S3	cervix:	n/a
3	chr4:55896358-55896408	Jurkat	blood:	n/a
4	chr4:55896358-55896408	GM12892	blood:	n/a
5	chr4:55896358-55896408	SKMC	muscle:	n/a
6	chr4:55896358-55896408	CMK	blood:	n/a
7	chr4:55896358-55896408	LNCaP	prostate:	n/a
8	chr4:55896358-55896408	AoSMC	blood vessel:	n/a
9	chr4:55896358-55896408	HIPEpiC	eye:	n/a
10	chr4:55896358-55896408	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:55896358-55896408	K562	blood:	n/a
12	chr4:55896358-55896408	HEEpiC	esophagus:	n/a
13	chr4:55896358-55896408	HCT-116	colon:	n/a
14	chr4:55896358-55896408	PANC-1	pancreas:	n/a
15	chr4:55896358-55896408	ProgFib	skin:	n/a
16	chr4:55896358-55896408	GM19239	blood:	n/a
17	chr4:55896358-55896408	HCF	heart:	n/a
18	chr4:55896358-55896408	RPTEC	kidney:	n/a
19	chr4:55896358-55896408	AG04450	lung:	fetal
20	chr4:55896358-55896408	PrEC	prostate:	n/a
21	chr4:55896358-55896408	AG09319	gingival:	n/a
22	chr4:55896358-55896408	HCM	heart:	n/a
23	chr4:55896358-55896408	GM06990	blood:	n/a
24	chr4:55896358-55896408	AG09309	skin:	n/a
25	chr4:55896358-55896408	SK-N-SH	brain:	n/a
26	chr4:55896358-55896408	SK-N-MC	brain:	n/a
27	chr4:55896358-55896408	T-47D	breast:	n/a
28	chr4:55896358-55896408	HRPEpiC	eye:	n/a
29	chr4:55896358-55896408	HUVEC	blood vessel:	n/a
30	chr4:55896358-55896408	HepG2	liver:	n/a
31	chr4:55896358-55896408	Hepatocyte	liver:	n/a
32	chr4:55896358-55896408	U87	brain:	n/a
33	chr4:55896358-55896408	IMR90	lung:	fetal
34	chr4:55896358-55896408	MCF10A-Er-Src	breast:	n/a
35	chr4:55896358-55896408	NH-A	brain:	n/a
36	chr4:55896358-55896408	HL-60	blood:	n/a
37	chr4:55896358-55896408	HMEC	breast:	n/a
38	chr4:55896358-55896408	HRCEpiC	kidney:	n/a
39	chr4:55896358-55896408	NT2-D1	testis:	n/a
40	chr4:55896358-55896408	HEK293	kidney:	embryo
41	chr4:55896358-55896408	BJ	skin:	n/a
42	chr4:55896358-55896408	NHDF-neo	bronchial:	n/a
43	chr4:55896358-55896408	AG10803	skin:	n/a
44	chr4:55896358-55896408	Caco-2	colon:	n/a
45	chr4:55896358-55896408	A549	lung:	n/a
46	chr4:55896358-55896408	HRE	kidney:	n/a
47	chr4:55896358-55896408	HNPCEpiC	eye:	n/a
48	chr4:55896358-55896408	ovcar-3	ovarian:	n/a
49	chr4:55896358-55896408	H1-hESC	embryonic stem cell:	embryo
50	chr4:55896358-55896408	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:55882690..55885444-chr4:55890043..55891620,2	K562	blood:
2	chr4:55894023..55896484-chr4:55898174..55900884,2	K562	blood:
3	chr4:55896634..55899178-chr4:55901546..55903412,2	K562	blood:
4	chr4:55896668..55899421-chr4:55901596..55903908,3	MCF-7	breast:
5	chr4:55879488..55881392-chr4:55899514..55901317,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRD5A3-2	chr4:55919227-55919264	ENSG00000250646.1

Variant related genes	Relation type
ENSG00000250646	TF binding region
RNU6-410P	TF binding region
ENSG00000250646	CpG island
RNU6-410P	CpG island
ENSG00000252815	chromatin interactions

Extended variants
information (count: 833 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4241988	chr4:55891531-55891532	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557560996	chr4:55891562-55891563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574262483	chr4:55891568-55891569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34222805	chr4:55891569-55891570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141096201	chr4:55891582-55891583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553553475	chr4:55891646-55891647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146958296	chr4:55891684-55891685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184134346	chr4:55891736-55891737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544631243	chr4:55891745-55891746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188802131	chr4:55891761-55891762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530488421	chr4:55891819-55891820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550280536	chr4:55891846-55891847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567047567	chr4:55891855-55891856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112502348	chr4:55891860-55891861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546428900	chr4:55891885-55891886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4582210	chr4:55891895-55891896	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs180775604	chr4:55891897-55891898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557835954	chr4:55891905-55891906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571640097	chr4:55891916-55891917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369931461	chr4:55891919-55891920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557475382	chr4:55891967-55891968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574227859	chr4:55891988-55891989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572093460	chr4:55891989-55891990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6826761	chr4:55891998-55891999	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78188715	chr4:55892000-55892001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185387947	chr4:55892003-55892004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564697848	chr4:55892009-55892010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539469074	chr4:55892017-55892018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369486700	chr4:55892044-55892045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527406878	chr4:55892084-55892085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543836375	chr4:55892094-55892095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560638597	chr4:55892115-55892116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372255091	chr4:55892120-55892121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546351276	chr4:55892176-55892177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150455856	chr4:55892203-55892204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532280386	chr4:55892251-55892252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552425838	chr4:55892279-55892280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569091501	chr4:55892289-55892290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566965657	chr4:55892303-55892304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551042054	chr4:55892348-55892349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567715113	chr4:55892506-55892507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548787765	chr4:55892526-55892527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536751466	chr4:55892567-55892568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553256581	chr4:55892596-55892597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369937540	chr4:55892650-55892651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534362124	chr4:55892667-55892668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577600470	chr4:55892676-55892677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113547439	chr4:55892774-55892775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138344595	chr4:55892789-55892790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191832652	chr4:55892805-55892806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55886400-55893800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:55890600-55892200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:55891000-55892000	Enhancers	HMEC	breast
4	chr4:55891200-55892200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:55891200-55892200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:55891200-55892200	Enhancers	NHEK	skin
7	chr4:55892000-55896800	Weak transcription	HMEC	breast
8	chr4:55892200-55896800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:55892200-55897400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:55893800-55894200	Enhancers	Placenta	Placenta
11	chr4:55893800-55894200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr4:55893800-55897200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr4:55894200-55898600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr4:55895600-55896400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:55895600-55897600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:55895800-55896600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:55895800-55897200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:55895800-55897600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:55895800-55904600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr4:55896000-55896200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:55896000-55896400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr4:55896000-55896400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:55896000-55896400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:55896000-55896600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:55896000-55897400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:55896200-55896400	Enhancers	Right Atrium	heart
27	chr4:55896400-55898600	Weak transcription	Right Atrium	heart
28	chr4:55896400-55898800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr4:55896400-55904400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:55896600-55898800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:55896600-55898800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr4:55896800-55897200	Enhancers	Adipose Nuclei	Adipose
33	chr4:55896800-55897800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:55896800-55905000	Enhancers	HMEC	breast
35	chr4:55897000-55897600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr4:55897200-55898200	Enhancers	Duodenum Mucosa	Duodenum
37	chr4:55897200-55898800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:55897400-55897600	Enhancers	Left Ventricle	heart
39	chr4:55897400-55898000	Enhancers	NHEK	skin
40	chr4:55897400-55898200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:55897400-55898600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:55897600-55898000	Enhancers	Fetal Intestine Small	intestine
43	chr4:55897600-55898200	Weak transcription	Left Ventricle	heart
44	chr4:55897600-55898400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:55897600-55898600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:55897600-55898600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:55897600-55898800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:55897800-55900000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:55898000-55898400	Weak transcription	Fetal Intestine Small	intestine
50	chr4:55898000-55902400	Weak transcription	NHEK	skin

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