Variant report

Variant	nsv870229
Chromosome Location	chr4:152114410-152161072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:438)
CpG islands
(count:427)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:152126195-152127277	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:152127772-152127935	HepG2	liver:	n/a	n/a
3	CCNT2	chr4:152136410-152136901	K562	blood:	n/a	n/a
4	CEBPB	chr4:152136678-152136872	MCF-7	breast:	n/a	n/a
5	CEBPB	chr4:152126139-152126588	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:152138809-152139024	A549	lung:	n/a	chr4:152138884-152138895
7	CEBPB	chr4:152149546-152149829	K562	blood:	n/a	chr4:152149719-152149728 chr4:152149719-152149728 chr4:152149717-152149728 chr4:152149719-152149728 chr4:152149719-152149728
8	CEBPB	chr4:152136675-152136912	K562	blood:	n/a	n/a
9	CEBPB	chr4:152123580-152123908	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:152147501-152148330	IMR90	lung:	n/a	chr4:152148168-152148181
11	CEBPB	chr4:152152369-152152378	K562	blood:	n/a	n/a
12	CEBPB	chr4:152126151-152126612	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:152126231-152126464	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:152126299-152126503	A549	lung:	n/a	n/a
15	CEBPB	chr4:152136649-152137059	MCF-7	breast:	n/a	n/a
16	CEBPB	chr4:152138739-152138989	IMR90	lung:	n/a	chr4:152138884-152138895
17	CEBPB	chr4:152149579-152149826	HepG2	liver:	n/a	chr4:152149719-152149728 chr4:152149719-152149728 chr4:152149717-152149728 chr4:152149719-152149728 chr4:152149719-152149728
18	CEBPB	chr4:152123580-152123872	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:152149531-152150187	IMR90	lung:	n/a	chr4:152149719-152149728 chr4:152149719-152149728 chr4:152149717-152149728 chr4:152149719-152149728 chr4:152149719-152149728
20	CEBPB	chr4:152123649-152123849	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:152138761-152138984	HepG2	liver:	n/a	chr4:152138884-152138895
22	CEBPB	chr4:152118487-152118693	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:152148139-152148334	K562	blood:	n/a	chr4:152148168-152148181
24	CHD2	chr4:152126352-152126598	HepG2	liver:	n/a	n/a
25	CTCF	chr4:152159807-152159924	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:152120800-152120950	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr4:152120700-152120850	BJ	skin:	n/a	n/a
28	CTCF	chr4:152159780-152159930	HMF	breast:	n/a	n/a
29	CTCF	chr4:152159760-152159910	AG04449	skin:	n/a	chr4:152159764-152159777
30	CTCF	chr4:152159759-152159956	HUVEC	blood vessel:	n/a	chr4:152159764-152159777
31	CTCF	chr4:152159740-152159890	HAc	cerebellar:	n/a	chr4:152159764-152159777
32	CTCF	chr4:152159720-152159870	NHLF	lung:	n/a	chr4:152159764-152159777
33	CTCF	chr4:152159760-152159910	HUVEC	blood vessel:	n/a	chr4:152159764-152159777
34	CTCF	chr4:152159780-152159930	AG09319	gingival:	n/a	n/a
35	CTCF	chr4:152159780-152159930	AG10803	skin:	n/a	n/a
36	CTCF	chr4:152116560-152116710	AG10803	skin:	n/a	n/a
37	CTCF	chr4:152159740-152159890	HRPEpiC	eye:	n/a	chr4:152159764-152159777
38	CTCF	chr4:152117400-152117550	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:152120800-152120950	AG09319	gingival:	n/a	n/a
40	CTCF	chr4:152117360-152117510	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:152159780-152159930	HCM	heart:	n/a	n/a
42	CTCF	chr4:152148840-152148990	AG09319	gingival:	n/a	n/a
43	CTCF	chr4:152159760-152159910	BE2_C	brain:	n/a	chr4:152159764-152159777
44	CTCF	chr4:152159780-152159930	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr4:152159721-152159916	GM12878	blood:	n/a	chr4:152159764-152159777
46	CTCF	chr4:152159740-152159890	MCF-7	breast:	n/a	chr4:152159764-152159777
47	CTCF	chr4:152134675-152134731	GM13977	blood:	n/a	n/a
48	CTCF	chr4:152159780-152159930	HRE	kidney:	n/a	n/a
49	CTCF	chr4:152159820-152159970	HMEC	breast:	n/a	n/a
50	CTCF	chr4:152120640-152120790	AG09319	gingival:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152147803-152147853	HL-60	blood:	n/a
2	chr4:152148822-152148872	PANC-1	pancreas:	n/a
3	chr4:152147390-152147440	ECC-1	luminal epithelium:	n/a
4	chr4:152147390-152147440	AG10803	skin:	n/a
5	chr4:152157274-152157324	ProgFib	skin:	n/a
6	chr4:152147803-152147853	AoSMC	blood vessel:	n/a
7	chr4:152157462-152157512	PrEC	prostate:	n/a
8	chr4:152148822-152148872	SKMC	muscle:	n/a
9	chr4:152120720-152120770	HMEC	breast:	n/a
10	chr4:152148822-152148872	HCM	heart:	n/a
11	chr4:152157274-152157324	PrEC	prostate:	n/a
12	chr4:152157274-152157324	K562	blood:	n/a
13	chr4:152157462-152157512	RPTEC	kidney:	n/a
14	chr4:152157274-152157324	Caco-2	colon:	n/a
15	chr4:152147803-152147853	CMK	blood:	n/a
16	chr4:152148822-152148872	AG09319	gingival:	n/a
17	chr4:152149064-152149114	SK-N-SH_RA	brain:	n/a
18	chr4:152157462-152157512	HAEpiC	amniotic membrane:	n/a
19	chr4:152148822-152148872	SK-N-MC	brain:	n/a
20	chr4:152157274-152157324	HCF	heart:	n/a
21	chr4:152147803-152147853	MCF10A-Er-Src	breast:	n/a
22	chr4:152147803-152147853	HIPEpiC	eye:	n/a
23	chr4:152147803-152147853	AG04450	lung:	fetal
24	chr4:152147390-152147440	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:152157462-152157512	GM06990	blood:	n/a
26	chr4:152120720-152120770	SKMC	muscle:	n/a
27	chr4:152148822-152148872	SK-N-SH	brain:	n/a
28	chr4:152157462-152157512	HUVEC	blood vessel:	n/a
29	chr4:152149064-152149114	T-47D	breast:	n/a
30	chr4:152148822-152148872	CMK	blood:	n/a
31	chr4:152157462-152157512	MCF10A-Er-Src	breast:	n/a
32	chr4:152157462-152157512	AG09309	skin:	n/a
33	chr4:152157274-152157324	HCPEpiC	choroid plexus:	n/a
34	chr4:152120720-152120770	ECC-1	luminal epithelium:	n/a
35	chr4:152148822-152148872	GM12878	blood:	n/a
36	chr4:152149064-152149114	HEK293	kidney:	embryo
37	chr4:152149064-152149114	SK-N-MC	brain:	n/a
38	chr4:152149064-152149114	HCT-116	colon:	n/a
39	chr4:152147803-152147853	BJ	skin:	n/a
40	chr4:152157462-152157512	HCM	heart:	n/a
41	chr4:152147390-152147440	HRPEpiC	eye:	n/a
42	chr4:152157462-152157512	AG10803	skin:	n/a
43	chr4:152157274-152157324	SKMC	muscle:	n/a
44	chr4:152157462-152157512	CMK	blood:	n/a
45	chr4:152120720-152120770	SAEC	small airway:	n/a
46	chr4:152147390-152147440	HAEpiC	amniotic membrane:	n/a
47	chr4:152148822-152148872	SAEC	small airway:	n/a
48	chr4:152157274-152157324	GM19239	blood:	n/a
49	chr4:152157462-152157512	PANC-1	pancreas:	n/a
50	chr4:152157462-152157512	HRPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:152124247..152127110-chr4:152129155..152131001,2	MCF-7	breast:
2	chr4:152108334..152110110-chr4:152112946..152114914,2	MCF-7	breast:
3	chr4:152116628..152118796-chr4:152119298..152121521,2	MCF-7	breast:
4	chr4:152159933..152162263-chr4:152163504..152165739,2	MCF-7	breast:
5	chr4:152125993..152128805-chr4:152246228..152247794,2	MCF-7	breast:
6	chr4:152124247..152127110-chr4:152129155..152131001,2	MCF-7	breast:
7	chr4:152114893..152116917-chr4:152120832..152122649,2	K562	blood:
8	chr4:152120488..152122139-chr4:152131128..152132730,2	K562	blood:
9	chr4:152111558..152113279-chr4:152114907..152117162,2	MCF-7	breast:
10	chr4:152120488..152122139-chr4:152131128..152132730,2	K562	blood:
11	chr4:152118284..152119881-chr4:152128835..152131528,2	K562	blood:
12	chr4:152116628..152118796-chr4:152119298..152121521,2	MCF-7	breast:
13	chr4:152114893..152116917-chr4:152120832..152122649,2	K562	blood:
14	chr4:152118284..152119881-chr4:152128835..152131528,2	K562	blood:

No data

Variant related genes	Relation type
SH3D19	TF binding region
SH3D19	CpG island
ENSG00000109686	chromatin interactions

Extended variants
information (count: 1669 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60067480	chr4:152114422-152114423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185889175	chr4:152114433-152114434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145151635	chr4:152114470-152114471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138968038	chr4:152114572-152114573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371491799	chr4:152114641-152114642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75487975	chr4:152114693-152114694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77904700	chr4:152114695-152114696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77208488	chr4:152114696-152114697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75536539	chr4:152114697-152114698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549845242	chr4:152114725-152114726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188397885	chr4:152114742-152114743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564488655	chr4:152114749-152114750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528983666	chr4:152114764-152114765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181172928	chr4:152114798-152114799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577043090	chr4:152114837-152114838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374088321	chr4:152114873-152114874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565753217	chr4:152114972-152114973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539654463	chr4:152114989-152114990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551258408	chr4:152115092-152115093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72723756	chr4:152115124-152115125	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs28585496	chr4:152115141-152115142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75379272	chr4:152115157-152115158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143051951	chr4:152115159-152115160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201719037	chr4:152115169-152115170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576185762	chr4:152115198-152115199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574048262	chr4:152115229-152115230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534821231	chr4:152115247-152115248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78296340	chr4:152115280-152115281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13125574	chr4:152115283-152115284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs200565393	chr4:152115286-152115287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545666489	chr4:152115322-152115323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190949329	chr4:152115326-152115327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576019568	chr4:152115345-152115346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543398093	chr4:152115399-152115400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561551753	chr4:152115470-152115471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148207831	chr4:152115535-152115536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368538753	chr4:152115593-152115594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200928245	chr4:152115629-152115630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375349161	chr4:152115634-152115635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6849352	chr4:152115670-152115671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528948839	chr4:152115671-152115672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375284817	chr4:152115686-152115687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559428445	chr4:152115710-152115711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532949681	chr4:152115716-152115717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182714124	chr4:152115723-152115724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569567586	chr4:152115750-152115751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs367882634	chr4:152115767-152115768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189524018	chr4:152115785-152115786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147395492	chr4:152115850-152115851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138133471	chr4:152115860-152115861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Intellectual disability	22102821	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152088200-152114600	Weak transcription	Psoas Muscle	Psoas
2	chr4:152096600-152118000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:152096800-152120600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr4:152097200-152123600	Weak transcription	Pancreas	Pancrea
5	chr4:152097200-152136600	Weak transcription	Colonic Mucosa	Colon
6	chr4:152097400-152123600	Weak transcription	Aorta	Aorta
7	chr4:152097600-152128800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:152097800-152117200	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:152097800-152120000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr4:152098200-152117000	Weak transcription	Brain Anterior Caudate	brain
11	chr4:152098200-152118400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:152098400-152116600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:152098400-152118400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr4:152098400-152147200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:152100200-152116600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:152100600-152118000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr4:152106600-152115600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr4:152106600-152116600	Weak transcription	NHEK	skin
19	chr4:152106600-152117200	Weak transcription	Left Ventricle	heart
20	chr4:152106800-152116600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:152107200-152116000	Weak transcription	Ovary	ovary
22	chr4:152107200-152120000	Weak transcription	HepG2	liver
23	chr4:152107600-152116600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr4:152111800-152116600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:152112000-152117200	Weak transcription	Lung	lung
26	chr4:152112200-152116600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:152112200-152117200	Weak transcription	Right Atrium	heart
28	chr4:152112200-152120000	Weak transcription	Right Ventricle	heart
29	chr4:152112400-152117200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:152112400-152117200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:152112400-152120600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:152112600-152116000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:152112600-152117200	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr4:152112600-152117400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr4:152112800-152120000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:152113400-152115000	Enhancers	Fetal Heart	heart
37	chr4:152113400-152124400	Weak transcription	Fetal Intestine Small	intestine
38	chr4:152113600-152114800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:152113600-152117200	Weak transcription	Brain Hippocampus Middle	brain
40	chr4:152113800-152114800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:152113800-152114800	Enhancers	Adipose Nuclei	Adipose
42	chr4:152113800-152115800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:152114400-152115000	Enhancers	NHDF-Ad	bronchial
44	chr4:152114400-152117000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr4:152114400-152117000	Weak transcription	HSMM	muscle
46	chr4:152114400-152117200	Weak transcription	Brain Substantia Nigra	brain
47	chr4:152114600-152115000	Enhancers	Psoas Muscle	Psoas
48	chr4:152114600-152115000	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr4:152114600-152115000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr4:152114800-152116600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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