Variant report

Variant	nsv881416
Chromosome Location	chr4:187903476-187943614
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	BACH1	chr4:187938365-187938620	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:187923294-187923654	IMR90	lung:	n/a	chr4:187923465-187923476
3	CEBPB	chr4:187923410-187923599	H1-hESC	embryonic stem cell:	n/a	chr4:187923465-187923476
4	CEBPB	chr4:187927557-187927886	IMR90	lung:	n/a	chr4:187927733-187927746
5	CEBPB	chr4:187923364-187923655	A549	lung:	n/a	chr4:187923465-187923476
6	CEBPB	chr4:187923457-187923475	K562	blood:	n/a	n/a
7	CEBPB	chr4:187930239-187930492	HepG2	liver:	n/a	chr4:187930359-187930370
8	CEBPB	chr4:187923422-187923659	HepG2	liver:	n/a	chr4:187923465-187923476
9	CTCF	chr4:187913446-187913502	Spleen_OC	spleen:	n/a	n/a
10	CTCF	chr4:187909000-187909081	GM20000	blood:	n/a	n/a
11	E2F4	chr4:187938334-187938602	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr4:187927430-187927884	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F6	chr4:187940904-187941499	H1-hESC	embryonic stem cell:	n/a	n/a
14	FOS	chr4:187931333-187931467	MCF10A-Er-Src	breast:	n/a	chr4:187931446-187931457
15	FOS	chr4:187931293-187931552	MCF10A-Er-Src	breast:	n/a	chr4:187931446-187931457
16	FOS	chr4:187927249-187927608	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr4:187938406-187938553	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr4:187927269-187927830	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:187938383-187938466	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:187927203-187927803	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr4:187931300-187931462	MCF10A-Er-Src	breast:	n/a	chr4:187931446-187931457
22	FOS	chr4:187927279-187927702	MCF10A-Er-Src	breast:	n/a	n/a
23	FOXP2	chr4:187941153-187941327	PFSK-1	brain:	n/a	n/a
24	GATA2	chr4:187935787-187936043	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr4:187935791-187936079	T-47D	breast:	n/a	chr4:187936045-187936058
26	GATA3	chr4:187924223-187924454	T-47D	breast:	n/a	n/a
27	GATA3	chr4:187935737-187936035	T-47D	breast:	n/a	n/a
28	JUN	chr4:187941381-187941412	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr4:187915553-187915604	HepG2	liver:	n/a	chr4:187915581-187915592 chr4:187915584-187915591 chr4:187915583-187915591 chr4:187915582-187915592 chr4:187915583-187915592
30	JUND	chr4:187941252-187941539	H1-hESC	embryonic stem cell:	n/a	n/a
31	JUND	chr4:187925213-187925489	HepG2	liver:	n/a	n/a
32	KAP1	chr4:187941011-187941530	U2OS	brain:	n/a	n/a
33	KAP1	chr4:187940870-187941514	HEK293	kidney:	n/a	n/a
34	MAFF	chr4:187938329-187938585	HepG2	liver:	n/a	n/a
35	MAFK	chr4:187916115-187916295	HepG2	liver:	n/a	chr4:187916191-187916202 chr4:187916186-187916202
36	MAFK	chr4:187915456-187915459	HepG2	liver:	n/a	n/a
37	MAFK	chr4:187907112-187907354	IMR90	lung:	n/a	n/a
38	MAFK	chr4:187938379-187938584	HepG2	liver:	n/a	chr4:187938460-187938471 chr4:187938460-187938471 chr4:187938455-187938470 chr4:187938455-187938471 chr4:187938459-187938470
39	MAFK	chr4:187938334-187938588	H1-hESC	embryonic stem cell:	n/a	chr4:187938460-187938471 chr4:187938460-187938471 chr4:187938455-187938470 chr4:187938455-187938471 chr4:187938459-187938470
40	MAFK	chr4:187906927-187907360	HepG2	liver:	n/a	n/a
41	MAFK	chr4:187938414-187938597	Hela-S3	cervix:	n/a	chr4:187938460-187938471 chr4:187938460-187938471 chr4:187938455-187938470 chr4:187938455-187938471 chr4:187938459-187938470
42	MAFK	chr4:187938300-187938623	HepG2	liver:	n/a	chr4:187938460-187938471 chr4:187938460-187938471 chr4:187938455-187938470 chr4:187938455-187938471 chr4:187938459-187938470
43	MAX	chr4:187940961-187941432	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr4:187940978-187941452	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr4:187941037-187941410	H1-hESC	embryonic stem cell:	n/a	n/a
46	MYC	chr4:187941144-187941258	H1-hESC	embryonic stem cell:	n/a	n/a
47	MYC	chr4:187927485-187927830	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr4:187927337-187927838	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr4:187938286-187938512	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr4:187938543-187938706	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187927166-187927216	NHBE	bronchial:	n/a
2	chr4:187927166-187927216	NHBE	bronchial:	n/a
3	chr4:187927166-187927216	NT2-D1	testis:	n/a
4	chr4:187927166-187927216	HCT-116	colon:	n/a
5	chr4:187927166-187927216	U87	brain:	n/a
6	chr4:187927166-187927216	NHDF-neo	bronchial:	n/a
7	chr4:187927166-187927216	H1-hESC	embryonic stem cell:	embryo
8	chr4:187927166-187927216	RPTEC	kidney:	n/a
9	chr4:187927166-187927216	HNPCEpiC	eye:	n/a
10	chr4:187927166-187927216	AG09319	gingival:	n/a
11	chr4:187927166-187927216	Hepatocyte	liver:	n/a
12	chr4:187927166-187927216	HepG2	liver:	n/a
13	chr4:187927166-187927216	MCF10A-Er-Src	breast:	n/a
14	chr4:187927166-187927216	IMR90	lung:	fetal
15	chr4:187927166-187927216	T-47D	breast:	n/a
16	chr4:187927166-187927216	HUVEC	blood vessel:	n/a
17	chr4:187927166-187927216	SK-N-MC	brain:	n/a
18	chr4:187927166-187927216	SAEC	small airway:	n/a
19	chr4:187927166-187927216	HRCEpiC	kidney:	n/a
20	chr4:187927166-187927216	HCPEpiC	choroid plexus:	n/a
21	chr4:187927166-187927216	AoSMC	blood vessel:	n/a
22	chr4:187927166-187927216	CMK	blood:	n/a
23	chr4:187927166-187927216	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:187927166-187927216	HRE	kidney:	n/a
25	chr4:187927166-187927216	BJ	skin:	n/a
26	chr4:187927166-187927216	GM06990	blood:	n/a
27	chr4:187927166-187927216	HIPEpiC	eye:	n/a
28	chr4:187927166-187927216	GM19239	blood:	n/a
29	chr4:187927166-187927216	K562	blood:	n/a
30	chr4:187927166-187927216	PFSK-1	brain:	n/a
31	chr4:187927166-187927216	HEEpiC	esophagus:	n/a
32	chr4:187927166-187927216	SK-N-SH	brain:	n/a
33	chr4:187927166-187927216	AG04449	skin:	fetal
34	chr4:187927166-187927216	HL-60	blood:	n/a
35	chr4:187927166-187927216	HCF	heart:	n/a
36	chr4:187927166-187927216	NH-A	brain:	n/a
37	chr4:187927166-187927216	GM12892	blood:	n/a
38	chr4:187927166-187927216	HRPEpiC	eye:	n/a
39	chr4:187927166-187927216	AG04450	lung:	fetal
40	chr4:187927166-187927216	ovcar-3	ovarian:	n/a
41	chr4:187927166-187927216	SK-N-SH_RA	brain:	n/a
42	chr4:187927166-187927216	HAEpiC	amniotic membrane:	n/a
43	chr4:187927166-187927216	Jurkat	blood:	n/a
44	chr4:187927166-187927216	GM12878	blood:	n/a
45	chr4:187927166-187927216	SKMC	muscle:	n/a
46	chr4:187927166-187927216	ECC-1	luminal epithelium:	n/a
47	chr4:187927166-187927216	HEK293	kidney:	embryo
48	chr4:187927166-187927216	HMEC	breast:	n/a
49	chr4:187927166-187927216	HCM	heart:	n/a
50	chr4:187927166-187927216	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187910556..187913594-chr4:187916872..187920065,3	K562	blood:
2	chr4:187939165..187941494-chr4:187941726..187943652,2	K562	blood:
3	chr4:187910556..187913594-chr4:187916872..187920065,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAT1-1	chr4:187943080-187943127	XLOC_004215
2	lnc-FAT1-1	chr4:187917410-187917592	XLOC_004215

Variant related genes	Relation type
ENSG00000249742	TF binding region
ENSG00000249742	CpG island
ENSG00000249742	chromatin interactions

Extended variants
information (count: 1503 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1503 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6835681	chr4:187903476-187903477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532833754	chr4:187903481-187903482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376474265	chr4:187903521-187903522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139050246	chr4:187903535-187903536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144049212	chr4:187903559-187903560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1030381	chr4:187903568-187903569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs76818274	chr4:187903628-187903629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538072916	chr4:187903659-187903660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550423119	chr4:187903660-187903661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534769833	chr4:187903677-187903678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571848417	chr4:187903686-187903687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558086716	chr4:187903727-187903728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577867220	chr4:187903768-187903769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1030382	chr4:187903782-187903783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs556498963	chr4:187903803-187903804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576327969	chr4:187903807-187903808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4571389	chr4:187903830-187903831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183846115	chr4:187903832-187903833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557824555	chr4:187903853-187903854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572968571	chr4:187903856-187903857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188949804	chr4:187903893-187903894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2375916	chr4:187903923-187903924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs4861733	chr4:187903933-187903934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs192287116	chr4:187903974-187903975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533663967	chr4:187904026-187904027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573744309	chr4:187904032-187904033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549543053	chr4:187904037-187904038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4862750	chr4:187904043-187904044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4862751	chr4:187904050-187904051	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549109471	chr4:187904101-187904102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184303427	chr4:187904175-187904176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76642501	chr4:187904176-187904177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376591336	chr4:187904215-187904216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190527709	chr4:187904222-187904223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146446072	chr4:187904228-187904229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182269093	chr4:187904367-187904368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537371766	chr4:187904395-187904396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139374191	chr4:187904406-187904407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576392021	chr4:187904480-187904481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186013250	chr4:187904515-187904516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372472656	chr4:187904532-187904533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189293951	chr4:187904561-187904562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111749260	chr4:187904562-187904563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181287262	chr4:187904578-187904579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542195637	chr4:187904594-187904595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369912973	chr4:187904647-187904648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544998557	chr4:187904658-187904659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150032552	chr4:187904670-187904671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578091201	chr4:187904676-187904677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116066918	chr4:187904757-187904758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Oral cancer	17325662	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187901800-187905000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:187902600-187904000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:187902600-187905400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:187902800-187904800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr4:187904000-187906600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:187904000-187909000	Weak transcription	Aorta	Aorta
7	chr4:187904800-187906200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr4:187905000-187906000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:187905400-187906200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:187911800-187942600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:187919800-187920000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:187920800-187921200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:187920800-187921200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:187920800-187921200	Enhancers	NHLF	lung
15	chr4:187920800-187921400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr4:187924000-187925400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr4:187925400-187927000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:187926000-187928200	Enhancers	Fetal Kidney	kidney
19	chr4:187926400-187927800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:187926400-187928200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:187927000-187927400	Enhancers	HMEC	breast
22	chr4:187927000-187927800	Enhancers	Fetal Stomach	stomach
23	chr4:187927000-187928200	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr4:187927000-187928200	Enhancers	Fetal Lung	lung
25	chr4:187927000-187928400	Enhancers	NHEK	skin
26	chr4:187927000-187928800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:187927200-187927800	Enhancers	Rectal Smooth Muscle	rectum
28	chr4:187927200-187928000	Enhancers	Osteobl	bone
29	chr4:187927200-187928200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:187927400-187927800	Flanking Active TSS	HMEC	breast
31	chr4:187927600-187928200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:187927800-187928400	Enhancers	HMEC	breast
33	chr4:187928000-187931200	Weak transcription	Osteobl	bone
34	chr4:187928200-187931000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:187931000-187931800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:187931200-187932000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr4:187931200-187932000	Enhancers	Osteobl	bone
38	chr4:187938000-187938600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:187938200-187938600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:187938200-187938600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:187938200-187938600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:187938200-187938800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:187938200-187939000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:187938400-187938600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:187938400-187938600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:187938400-187938600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:187938600-187939000	Enhancers	Fetal Kidney	kidney
48	chr4:187938600-187941000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:187938600-187941000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr4:187938800-187940800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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