Variant report

Variant	nsv470050
Chromosome Location	chr4:88186509-88228228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:453 , 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	ARID3A	chr4:88196507-88196704	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:88195615-88195678	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:88199339-88199978	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:88191313-88191649	HepG2	liver:	n/a	n/a
5	ATF2	chr4:88227105-88227643	GM12878	blood:	n/a	n/a
6	ATF2	chr4:88227219-88227557	GM12878	blood:	n/a	n/a
7	ATF3	chr4:88223744-88223892	K562	blood:	n/a	n/a
8	ATF3	chr4:88199339-88199930	HepG2	liver:	n/a	n/a
9	ATF3	chr4:88199549-88199769	HepG2	liver:	n/a	n/a
10	BACH1	chr4:88191402-88191656	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:88228029-88228308	GM12878	blood:	n/a	n/a
12	BATF	chr4:88227243-88227499	GM12878	blood:	n/a	chr4:88227386-88227397
13	BCL3	chr4:88225796-88226325	A549	lung:	n/a	n/a
14	BCL3	chr4:88227213-88227544	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:88199420-88199720	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:88199328-88199876	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:88199507-88199750	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:88225715-88226363	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:88191281-88191673	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr4:88207920-88208188	K562	blood:	n/a	n/a
21	CBX3	chr4:88215016-88215405	K562	blood:	n/a	n/a
22	CEBPB	chr4:88222910-88223189	K562	blood:	n/a	chr4:88223035-88223046
23	CEBPB	chr4:88222884-88223200	IMR90	lung:	n/a	chr4:88223035-88223046
24	CEBPB	chr4:88222901-88223173	A549	lung:	n/a	chr4:88223035-88223046
25	CEBPB	chr4:88197413-88197511	HepG2	liver:	n/a	chr4:88197420-88197431
26	CEBPB	chr4:88222879-88223179	HepG2	liver:	n/a	chr4:88223035-88223046
27	CEBPB	chr4:88195585-88195771	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:88225700-88226496	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:88226731-88227502	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:88225791-88226474	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:88199523-88199974	HepG2	liver:	n/a	n/a
32	CREB1	chr4:88227197-88227666	GM12878	blood:	n/a	n/a
33	CTCF	chr4:88191460-88191610	HCM	heart:	n/a	n/a
34	CTCF	chr4:88191440-88191590	AG04450	lung:	n/a	n/a
35	CTCF	chr4:88191392-88191595	Fibrobl	skin:	n/a	n/a
36	CTCF	chr4:88191394-88191598	GM12878	blood:	n/a	n/a
37	CTCF	chr4:88191454-88191547	GM12892	blood:	n/a	n/a
38	CTCF	chr4:88191380-88191530	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr4:88191440-88191590	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr4:88191480-88191630	GM12869	blood:	n/a	n/a
41	CTCF	chr4:88191400-88191550	A549	lung:	n/a	n/a
42	CTCF	chr4:88191460-88191610	GM12870	blood:	n/a	n/a
43	CTCF	chr4:88191440-88191590	HAc	cerebellar:	n/a	n/a
44	CTCF	chr4:88191420-88191570	GM12867	blood:	n/a	n/a
45	CTCF	chr4:88191400-88191550	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr4:88191380-88191530	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:88191377-88191608	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr4:88191480-88191630	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:88191373-88191618	HepG2	liver:	n/a	n/a
50	CTCF	chr4:88191460-88191610	WI-38	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88225834-88225884	NHBE	bronchial:	n/a
2	chr4:88225834-88225884	ovcar-3	ovarian:	n/a
3	chr4:88225834-88225884	SK-N-MC	brain:	n/a
4	chr4:88225834-88225884	Hepatocyte	liver:	n/a
5	chr4:88225834-88225884	SAEC	small airway:	n/a
6	chr4:88225834-88225884	Caco-2	colon:	n/a
7	chr4:88225834-88225884	NB4	blood:	n/a
8	chr4:88225834-88225884	HMEC	breast:	n/a
9	chr4:88225834-88225884	H1-hESC	embryonic stem cell:	embryo
10	chr4:88225834-88225884	AG09309	skin:	n/a
11	chr4:88225834-88225884	SK-N-SH_RA	brain:	n/a
12	chr4:88225834-88225884	HEEpiC	esophagus:	n/a
13	chr4:88225834-88225884	PFSK-1	brain:	n/a
14	chr4:88225834-88225884	GM19239	blood:	n/a
15	chr4:88225834-88225884	A549	lung:	n/a
16	chr4:88225834-88225884	GM12878	blood:	n/a
17	chr4:88225834-88225884	HCPEpiC	choroid plexus:	n/a
18	chr4:88225834-88225884	HNPCEpiC	eye:	n/a
19	chr4:88225834-88225884	HRPEpiC	eye:	n/a
20	chr4:88225834-88225884	AG09319	gingival:	n/a
21	chr4:88225834-88225884	NHDF-neo	bronchial:	n/a
22	chr4:88225834-88225884	AG04450	lung:	fetal
23	chr4:88225834-88225884	GM12891	blood:	n/a
24	chr4:88225834-88225884	HCT-116	colon:	n/a
25	chr4:88225834-88225884	AoSMC	blood vessel:	n/a
26	chr4:88225834-88225884	HEK293	kidney:	embryo
27	chr4:88225834-88225884	AG10803	skin:	n/a
28	chr4:88225834-88225884	ECC-1	luminal epithelium:	n/a
29	chr4:88225834-88225884	SK-N-SH	brain:	n/a
30	chr4:88225834-88225884	CMK	blood:	n/a
31	chr4:88225834-88225884	Jurkat	blood:	n/a
32	chr4:88225834-88225884	AG04449	skin:	fetal
33	chr4:88225834-88225884	SKMC	muscle:	n/a
34	chr4:88225834-88225884	BE2_C	brain:	n/a
35	chr4:88225834-88225884	HepG2	liver:	n/a
36	chr4:88225834-88225884	K562	blood:	n/a
37	chr4:88225834-88225884	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:88225834-88225884	RPTEC	kidney:	n/a
39	chr4:88225834-88225884	U87	brain:	n/a
40	chr4:88225834-88225884	NH-A	brain:	n/a
41	chr4:88225834-88225884	HL-60	blood:	n/a
42	chr4:88225834-88225884	HUVEC	blood vessel:	n/a
43	chr4:88225834-88225884	HAEpiC	amniotic membrane:	n/a
44	chr4:88225834-88225884	MCF-7	breast:	n/a
45	chr4:88225834-88225884	HRE	kidney:	n/a
46	chr4:88225834-88225884	IMR90	lung:	fetal
47	chr4:88225834-88225884	BJ	skin:	n/a
48	chr4:88225834-88225884	MCF10A-Er-Src	breast:	n/a
49	chr4:88225834-88225884	ProgFib	skin:	n/a
50	chr4:88225834-88225884	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
2	chr4:88132419..88135036-chr4:88191101..88193543,2	K562	blood:
3	chr10:46970031..46970993-chr4:88194361..88194882,2	MCF-7	breast:
4	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
5	chr4:88140123..88141719-chr4:88189481..88191440,2	MCF-7	breast:
6	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
7	chr4:88183411..88186658-chr4:88187924..88190841,3	K562	blood:
8	chr4:88190901..88191577-chr4:88769909..88770797,2	MCF-7	breast:
9	chr4:88161337..88162947-chr4:88190418..88192890,2	K562	blood:
10	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
11	chr4:88141337..88143545-chr4:88209433..88211061,2	MCF-7	breast:
12	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
13	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AFF1-1	chr4:88199776-88199855	XLOC_003601
2	lnc-AFF1-1	chr4:88192262-88192330	XLOC_003601
3	lnc-AFF1-1	chr4:88198781-88198895	XLOC_003601
4	lnc-HSD17B13-1	chr4:88187887-88187974	XLOC_004009

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5705	chr4:88221657-88221679	MIMAT0022499

No data

Variant related genes	Relation type
MIR5705	TF binding region
ENSG00000250572	TF binding region
MIR5705	CpG island
ENSG00000250572	CpG island
ENSG00000204176	chromatin interactions
ENSG00000250572	chromatin interactions
ENSG00000145332	chromatin interactions
CREG1	miRNA target sites

Extended variants
information (count: 1116 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7694379	chr4:88186509-88186510	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs561896900	chr4:88186560-88186561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192803653	chr4:88186578-88186579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185256222	chr4:88186597-88186598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190090225	chr4:88186674-88186675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556425228	chr4:88186705-88186706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182264192	chr4:88186713-88186714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552114547	chr4:88186714-88186715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11723697	chr4:88186722-88186723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185609340	chr4:88186726-88186727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187979905	chr4:88186813-88186814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574385127	chr4:88186820-88186821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535644649	chr4:88186833-88186834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10428496	chr4:88186905-88186906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575967508	chr4:88186906-88186907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545852432	chr4:88186924-88186925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557781602	chr4:88186929-88186930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573000364	chr4:88186946-88186947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114668031	chr4:88186971-88186972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561596214	chr4:88187058-88187059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142089617	chr4:88187062-88187063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544032389	chr4:88187067-88187068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151168306	chr4:88187086-88187087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533049085	chr4:88187139-88187140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542196972	chr4:88187157-88187158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140236704	chr4:88187166-88187167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs180848125	chr4:88187171-88187172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536934051	chr4:88187192-88187193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528598239	chr4:88187270-88187271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552575591	chr4:88187312-88187313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547092874	chr4:88187377-88187378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568414483	chr4:88187409-88187410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375637026	chr4:88187444-88187445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73839168	chr4:88187528-88187529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190067275	chr4:88187595-88187596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181413528	chr4:88187677-88187678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535063051	chr4:88187741-88187742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186880653	chr4:88187746-88187747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569616106	chr4:88187768-88187769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540114208	chr4:88187787-88187788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557818292	chr4:88187854-88187855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143458874	chr4:88187870-88187871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371344398	chr4:88187871-88187872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115025907	chr4:88187879-88187880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201690294	chr4:88187881-88187882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201032236	chr4:88187882-88187883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577973996	chr4:88187883-88187884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs66681228	chr4:88187884-88187885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369828102	chr4:88187888-88187889	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs555444829	chr4:88187927-88187928	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88184600-88191400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:88186200-88187600	Weak transcription	Aorta	Aorta
3	chr4:88187600-88188400	Enhancers	Aorta	Aorta
4	chr4:88187800-88189200	Enhancers	Adipose Nuclei	Adipose
5	chr4:88188000-88188200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:88188000-88188400	Enhancers	Fetal Kidney	kidney
7	chr4:88188200-88188600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:88188400-88188800	Weak transcription	Fetal Kidney	kidney
9	chr4:88188600-88189400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:88188800-88189600	Enhancers	Fetal Kidney	kidney
11	chr4:88188800-88190000	Enhancers	Colon Smooth Muscle	Colon
12	chr4:88189800-88190000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
13	chr4:88190400-88190600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:88190600-88191800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:88191200-88191600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr4:88191200-88192200	Enhancers	Brain Hippocampus Middle	brain
17	chr4:88191400-88192000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:88191600-88192000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr4:88191600-88192200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:88191600-88192200	Enhancers	Brain Anterior Caudate	brain
21	chr4:88191800-88192200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:88191800-88192200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:88191800-88192200	Enhancers	Brain Angular Gyrus	brain
24	chr4:88191800-88192200	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr4:88191800-88192200	Enhancers	Hela-S3	cervix
26	chr4:88191800-88192400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:88191800-88192400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr4:88191800-88192400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:88191800-88192400	Enhancers	Liver	Liver
30	chr4:88191800-88192400	Enhancers	HepG2	liver
31	chr4:88191800-88192600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:88192200-88192400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:88192400-88193200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr4:88192400-88196000	Weak transcription	Liver	Liver
35	chr4:88192600-88193000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:88193000-88193400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:88193400-88193600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr4:88193400-88193600	Enhancers	HepG2	liver
39	chr4:88193400-88194400	Enhancers	Stomach Mucosa	stomach
40	chr4:88193600-88195400	Weak transcription	HepG2	liver
41	chr4:88194400-88196000	Weak transcription	Stomach Mucosa	stomach
42	chr4:88195400-88197000	Enhancers	HepG2	liver
43	chr4:88195800-88196400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:88196000-88196200	Enhancers	Fetal Intestine Large	intestine
45	chr4:88196000-88196400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr4:88196000-88196400	Enhancers	Liver	Liver
47	chr4:88196200-88196400	Enhancers	Stomach Mucosa	stomach
48	chr4:88196200-88196400	Bivalent Enhancer	NHDF-Ad	bronchial
49	chr4:88196200-88196600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr4:88196400-88199200	Weak transcription	Liver	Liver

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