Variant report

Variant	nsv830143
Chromosome Location	chr4:167386232-167538014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:688)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:167422943-167423479	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:167402837-167403336	GM12878	blood:	n/a	n/a
3	ATF2	chr4:167402894-167403312	GM12878	blood:	n/a	n/a
4	ATF3	chr4:167423063-167423487	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:167423072-167423419	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:167489118-167489236	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:167423095-167423380	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:167402811-167403225	GM12878	blood:	n/a	chr4:167402976-167402987
9	BATF	chr4:167448712-167449039	GM12878	blood:	n/a	n/a
10	BATF	chr4:167402235-167402454	GM12878	blood:	n/a	n/a
11	BATF	chr4:167402867-167403200	GM12878	blood:	n/a	chr4:167402976-167402987
12	BCL11A	chr4:167402857-167403289	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:167448711-167449006	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:167448647-167448992	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:167501286-167501687	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:167402945-167403257	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:167501050-167501864	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:167421014-167421210	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:167423134-167423289	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr4:167515545-167515688	HepG2	liver:	n/a	n/a
21	CBX3	chr4:167515547-167515801	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:167423056-167423452	H1-hESC	embryonic stem cell:	n/a	chr4:167423248-167423259
23	CEBPB	chr4:167423070-167423403	HepG2	liver:	n/a	chr4:167423248-167423259
24	CEBPB	chr4:167403932-167404195	HepG2	liver:	n/a	chr4:167404015-167404026 chr4:167404017-167404028
25	CEBPB	chr4:167423135-167423385	Hela-S3	cervix:	n/a	chr4:167423248-167423259
26	CEBPB	chr4:167423138-167423262	HepG2	liver:	n/a	chr4:167423248-167423259
27	CEBPB	chr4:167441123-167441447	HepG2	liver:	n/a	chr4:167441263-167441274
28	CEBPB	chr4:167423114-167423505	MCF-7	breast:	n/a	chr4:167423248-167423259
29	CHD1	chr4:167448698-167448793	GM12878	blood:	n/a	n/a
30	CHD1	chr4:167430551-167430554	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr4:167422992-167423565	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:167402969-167403233	GM12878	blood:	n/a	n/a
33	CHD2	chr4:167423890-167423906	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr4:167422927-167423519	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr4:167423094-167423513	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:167515560-167515710	HAc	cerebellar:	n/a	n/a
37	CTCF	chr4:167423055-167423333	K562	blood:	n/a	n/a
38	CTCF	chr4:167515560-167515710	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr4:167515580-167515730	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:167515620-167515770	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr4:167515620-167515770	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr4:167515600-167515750	GM06990	blood:	n/a	n/a
43	CTCF	chr4:167515780-167515930	A549	lung:	n/a	n/a
44	CTCF	chr4:167423100-167423250	HPF	lung:	n/a	n/a
45	CTCF	chr4:167515620-167515770	AG04450	lung:	n/a	n/a
46	CTCF	chr4:167515680-167515830	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr4:167515640-167515790	GM12865	blood:	n/a	n/a
48	CTCF	chr4:167423112-167423345	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:167515580-167515730	GM12873	blood:	n/a	n/a
50	CTCF	chr4:167501440-167501505	Pancreas_OC	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:167448796-167448846	GM19239	blood:	n/a
2	chr4:167448796-167448846	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:167448796-167448846	RPTEC	kidney:	n/a
4	chr4:167448796-167448846	GM12892	blood:	n/a
5	chr4:167448796-167448846	GM12878	blood:	n/a
6	chr4:167448796-167448846	HL-60	blood:	n/a
7	chr4:167448796-167448846	GM06990	blood:	n/a
8	chr4:167448796-167448846	NHDF-neo	bronchial:	n/a
9	chr4:167448796-167448846	ECC-1	luminal epithelium:	n/a
10	chr4:167448796-167448846	PANC-1	pancreas:	n/a
11	chr4:167448796-167448846	SAEC	small airway:	n/a
12	chr4:167448796-167448846	MCF-7	breast:	n/a
13	chr4:167448796-167448846	AG04449	skin:	fetal
14	chr4:167448796-167448846	CMK	blood:	n/a
15	chr4:167448796-167448846	SKMC	muscle:	n/a
16	chr4:167448796-167448846	SK-N-MC	brain:	n/a
17	chr4:167448796-167448846	NT2-D1	testis:	n/a
18	chr4:167448796-167448846	HAEpiC	amniotic membrane:	n/a
19	chr4:167448796-167448846	HEEpiC	esophagus:	n/a
20	chr4:167448796-167448846	Hepatocyte	liver:	n/a
21	chr4:167448796-167448846	LNCaP	prostate:	n/a
22	chr4:167448796-167448846	AG04450	lung:	fetal
23	chr4:167448796-167448846	HIPEpiC	eye:	n/a
24	chr4:167448796-167448846	HNPCEpiC	eye:	n/a
25	chr4:167448796-167448846	A549	lung:	n/a
26	chr4:167448796-167448846	HUVEC	blood vessel:	n/a
27	chr4:167448796-167448846	GM12891	blood:	n/a
28	chr4:167448796-167448846	ProgFib	skin:	n/a
29	chr4:167448796-167448846	MCF10A-Er-Src	breast:	n/a
30	chr4:167448796-167448846	HRPEpiC	eye:	n/a
31	chr4:167448796-167448846	NHBE	bronchial:	n/a
32	chr4:167448796-167448846	HRCEpiC	kidney:	n/a
33	chr4:167448796-167448846	U87	brain:	n/a
34	chr4:167448796-167448846	Hela-S3	cervix:	n/a
35	chr4:167448796-167448846	BE2_C	brain:	n/a
36	chr4:167448796-167448846	IMR90	lung:	fetal
37	chr4:167448796-167448846	Caco-2	colon:	n/a
38	chr4:167448796-167448846	HEK293	kidney:	embryo
39	chr4:167448796-167448846	HepG2	liver:	n/a
40	chr4:167448796-167448846	SK-N-SH	brain:	n/a
41	chr4:167448796-167448846	ovcar-3	ovarian:	n/a
42	chr4:167448796-167448846	HCM	heart:	n/a
43	chr4:167448796-167448846	HCT-116	colon:	n/a
44	chr4:167448796-167448846	HCPEpiC	choroid plexus:	n/a
45	chr4:167448796-167448846	AG09319	gingival:	n/a
46	chr4:167448796-167448846	BJ	skin:	n/a
47	chr4:167448796-167448846	AG10803	skin:	n/a
48	chr4:167448796-167448846	T-47D	breast:	n/a
49	chr4:167448796-167448846	NB4	blood:	n/a
50	chr4:167448796-167448846	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:167484390..167486125-chr4:167489099..167491015,2	MCF-7	breast:
2	chr4:167086761..167087587-chr4:167515275..167516081,4	MCF-7	breast:
3	chr4:167423153..167423656-chr4:167515182..167515903,2	MCF-7	breast:
4	chr4:167524991..167527331-chr4:167531005..167532808,2	K562	blood:
5	chr4:167245228..167246184-chr4:167515396..167516066,3	MCF-7	breast:
6	chr4:167484390..167486125-chr4:167489099..167491015,2	MCF-7	breast:
7	chr4:167407304..167409099-chr4:167497184..167500129,2	K562	blood:
8	chr4:167407304..167409099-chr4:167497184..167500129,2	K562	blood:
9	chr4:167524991..167527331-chr4:167531005..167532808,2	K562	blood:
10	chr4:167090069..167090971-chr4:167515205..167515895,2	MCF-7	breast:
11	chr4:167423153..167423656-chr4:167515182..167515903,2	MCF-7	breast:
12	chr4:167244994..167245863-chr4:167515216..167516030,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000249675	TF binding region
ENSG00000249675	CpG island

Extended variants
information (count: 2750 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571298111	chr4:167402219-167402220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2322567	chr4:167402221-167402222	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574082315	chr4:167402228-167402229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543083631	chr4:167402329-167402330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561908522	chr4:167402347-167402348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548042296	chr4:167402362-167402363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566254147	chr4:167402376-167402377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536814880	chr4:167402393-167402394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11731744	chr4:167402443-167402444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548059941	chr4:167402472-167402473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2322566	chr4:167402513-167402514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368655455	chr4:167402517-167402518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190453576	chr4:167402521-167402522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372209377	chr4:167402594-167402595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183059452	chr4:167402641-167402642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141273337	chr4:167402645-167402646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74767395	chr4:167402648-167402649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368251863	chr4:167402706-167402707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567544246	chr4:167402715-167402716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542766537	chr4:167402746-167402747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188876570	chr4:167402757-167402758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531630709	chr4:167402761-167402762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549549292	chr4:167402811-167402812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193111313	chr4:167402854-167402855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs28887807	chr4:167402903-167402904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145014740	chr4:167402971-167402972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565748514	chr4:167402980-167402981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187671411	chr4:167402988-167402989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199792354	chr4:167402991-167402992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs56185534	chr4:167403005-167403006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570300359	chr4:167403013-167403014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537741373	chr4:167403019-167403020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143402868	chr4:167403098-167403099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375022496	chr4:167403099-167403100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111893536	chr4:167403118-167403119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535065793	chr4:167403138-167403139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142610190	chr4:167403150-167403151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534663057	chr4:167403298-167403299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11737269	chr4:167403307-167403308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553059627	chr4:167403396-167403397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375862432	chr4:167403521-167403522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574545667	chr4:167403523-167403524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191537941	chr4:167403539-167403540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3920008	chr4:167403606-167403607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184110285	chr4:167403607-167403608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553680941	chr4:167403700-167403701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10612714	chr4:167403714-167403715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs398108277	chr4:167403715-167403716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35656991	chr4:167403717-167403718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542601005	chr4:167403718-167403719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	17603634	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	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
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
Congenital diaphragmatic hernia	21085971	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
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Epilepsy	21635232	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167402200-167402600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:167402400-167402600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:167402400-167402800	Enhancers	GM12878-XiMat	blood
4	chr4:167402400-167403000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:167402400-167403000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:167402400-167403400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:167403000-167404000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:167403400-167404600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:167404000-167404400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:167404000-167404800	Enhancers	Primary hematopoietic stem cells	blood
11	chr4:167406600-167408200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr4:167407200-167408800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:167407600-167408600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:167408600-167415000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:167408600-167415200	Weak transcription	Fetal Intestine Small	intestine
16	chr4:167409600-167409800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:167409600-167409800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:167412800-167413200	Enhancers	Fetal Intestine Large	intestine
19	chr4:167413200-167414200	Weak transcription	Fetal Intestine Large	intestine
20	chr4:167414200-167416000	Enhancers	Fetal Intestine Large	intestine
21	chr4:167415000-167415400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:167415000-167415400	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:167415000-167415600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:167415000-167415800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:167415000-167415800	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr4:167415200-167416400	Enhancers	Fetal Intestine Small	intestine
27	chr4:167415400-167415800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:167415600-167416000	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:167415600-167420400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:167415800-167416400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:167416000-167419000	Weak transcription	Fetal Intestine Large	intestine
32	chr4:167416400-167418200	Weak transcription	Fetal Intestine Small	intestine
33	chr4:167417200-167417400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:167418200-167418800	Enhancers	Fetal Intestine Small	intestine
35	chr4:167418800-167419400	Weak transcription	Fetal Intestine Small	intestine
36	chr4:167419000-167420000	Enhancers	Fetal Intestine Large	intestine
37	chr4:167419200-167419600	Enhancers	Fetal Brain Male	brain
38	chr4:167419200-167420000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:167419200-167420400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr4:167419400-167419600	Enhancers	Fetal Intestine Small	intestine
41	chr4:167419400-167419800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:167419400-167420000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr4:167419400-167420000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:167419400-167420000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr4:167419600-167420000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:167419600-167420000	Enhancers	Brain Hippocampus Middle	brain
47	chr4:167419600-167420600	Enhancers	Fetal Stomach	stomach
48	chr4:167419600-167420800	Weak transcription	Fetal Brain Male	brain
49	chr4:167419800-167420000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr4:167420000-167421200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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