Variant report

Variant	nsv1019205
Chromosome Location	chr4:148524852-148576265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:733)
CpG islands
(count:915)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:148538402-148538707	K562	blood:	n/a	n/a
2	ARID3A	chr4:148528625-148528960	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:148538271-148539211	HepG2	liver:	n/a	n/a
4	ATF2	chr4:148538097-148538919	GM12878	blood:	n/a	n/a
5	ATF2	chr4:148538188-148538604	GM12878	blood:	n/a	n/a
6	BACH1	chr4:148548031-148548423	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:148538218-148538481	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr4:148538244-148539306	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:148535176-148535480	K562	blood:	n/a	n/a
10	BHLHE40	chr4:148538233-148539032	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:148538234-148538991	K562	blood:	n/a	n/a
12	BHLHE40	chr4:148560196-148560321	GM12878	blood:	n/a	n/a
13	BRCA1	chr4:148538476-148538636	HepG2	liver:	n/a	n/a
14	CBX3	chr4:148538144-148538965	K562	blood:	n/a	n/a
15	CCNT2	chr4:148538212-148538959	K562	blood:	n/a	chr4:148538420-148538429
16	CEBPB	chr4:148538322-148538539	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:148544957-148545208	HepG2	liver:	n/a	chr4:148545060-148545071
18	CEBPB	chr4:148538154-148538792	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr4:148538169-148538758	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:148538205-148538573	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr4:148538090-148538601	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:148538222-148538732	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:148538320-148538475	K562	blood:	n/a	n/a
24	CEBPB	chr4:148538172-148538675	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr4:148528661-148529047	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:148544939-148545170	IMR90	lung:	n/a	chr4:148545060-148545071
27	CEBPB	chr4:148538237-148538575	K562	blood:	n/a	n/a
28	CEBPB	chr4:148538179-148538683	K562	blood:	n/a	n/a
29	CEBPB	chr4:148538247-148538564	A549	lung:	n/a	n/a
30	CEBPB	chr4:148569392-148569517	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:148538242-148538717	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPD	chr4:148538316-148538556	HepG2	liver:	n/a	n/a
33	CEBPZ	chr4:148538344-148538542	HepG2	liver:	n/a	n/a
34	CHD2	chr4:148538223-148538721	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:148538167-148539207	GM12878	blood:	n/a	n/a
36	CHD2	chr4:148538169-148538797	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr4:148538229-148538936	K562	blood:	n/a	n/a
38	CHD2	chr4:148537595-148537597	GM12878	blood:	n/a	n/a
39	CHD2	chr4:148538316-148538807	HepG2	liver:	n/a	n/a
40	CREB1	chr4:148538133-148538897	HepG2	liver:	n/a	n/a
41	CREB1	chr4:148538265-148538720	A549	lung:	n/a	n/a
42	CREB1	chr4:148538149-148539089	GM12878	blood:	n/a	n/a
43	CTCF	chr4:148538660-148538810	Caco-2	colon:	n/a	n/a
44	CTCF	chr4:148538860-148539010	HVMF	connective:	n/a	chr4:148538958-148538971
45	CTCF	chr4:148538660-148538810	GM12875	blood:	n/a	n/a
46	CTCF	chr4:148538560-148538710	GM12871	blood:	n/a	n/a
47	CTCF	chr4:148538416-148538848	IMR90	lung:	n/a	chr4:148538803-148538816
48	CTCF	chr4:148538344-148538643	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr4:148538680-148538830	NHDF-neo	bronchial:	n/a	chr4:148538803-148538816
50	CTCF	chr4:148538660-148538810	SK-N-SH_RA	brain:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148535164-148535214	HRPEpiC	eye:	n/a
2	chr4:148538521-148538571	SK-N-SH	brain:	n/a
3	chr4:148559892-148559942	AG04450	lung:	fetal
4	chr4:148542561-148542611	ProgFib	skin:	n/a
5	chr4:148559892-148559942	NHDF-neo	bronchial:	n/a
6	chr4:148538641-148538691	HMEC	breast:	n/a
7	chr4:148535164-148535214	GM19239	blood:	n/a
8	chr4:148538527-148538577	HEK293	kidney:	embryo
9	chr4:148559892-148559942	SK-N-SH_RA	brain:	n/a
10	chr4:148559892-148559942	GM06990	blood:	n/a
11	chr4:148538817-148538867	HCF	heart:	n/a
12	chr4:148538527-148538577	RPTEC	kidney:	n/a
13	chr4:148538954-148539004	MCF-7	breast:	n/a
14	chr4:148538641-148538691	Hepatocyte	liver:	n/a
15	chr4:148538521-148538571	AG09319	gingival:	n/a
16	chr4:148559892-148559942	AG09319	gingival:	n/a
17	chr4:148538494-148538544	H1-hESC	embryonic stem cell:	embryo
18	chr4:148538521-148538571	U87	brain:	n/a
19	chr4:148538527-148538577	H1-hESC	embryonic stem cell:	embryo
20	chr4:148542561-148542611	AG09309	skin:	n/a
21	chr4:148538343-148538393	HAEpiC	amniotic membrane:	n/a
22	chr4:148538264-148538314	HEEpiC	esophagus:	n/a
23	chr4:148538494-148538544	HCPEpiC	choroid plexus:	n/a
24	chr4:148538954-148539004	HIPEpiC	eye:	n/a
25	chr4:148538143-148538193	HCF	heart:	n/a
26	chr4:148535164-148535214	MCF10A-Er-Src	breast:	n/a
27	chr4:148538491-148538541	Caco-2	colon:	n/a
28	chr4:148538343-148538393	Hela-S3	cervix:	n/a
29	chr4:148538264-148538314	LNCaP	prostate:	n/a
30	chr4:148538229-148538279	GM12878	blood:	n/a
31	chr4:148555806-148555856	GM06990	blood:	n/a
32	chr4:148538143-148538193	Hela-S3	cervix:	n/a
33	chr4:148538491-148538541	HCPEpiC	choroid plexus:	n/a
34	chr4:148538641-148538691	GM06990	blood:	n/a
35	chr4:148559892-148559942	GM12878	blood:	n/a
36	chr4:148538527-148538577	AG09319	gingival:	n/a
37	chr4:148538491-148538541	CMK	blood:	n/a
38	chr4:148538527-148538577	HRCEpiC	kidney:	n/a
39	chr4:148555806-148555856	HEEpiC	esophagus:	n/a
40	chr4:148538954-148539004	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:148538954-148539004	AG10803	skin:	n/a
42	chr4:148538521-148538571	A549	lung:	n/a
43	chr4:148538527-148538577	SK-N-MC	brain:	n/a
44	chr4:148538143-148538193	NHDF-neo	bronchial:	n/a
45	chr4:148538817-148538867	GM06990	blood:	n/a
46	chr4:148538521-148538571	SKMC	muscle:	n/a
47	chr4:148535164-148535214	PrEC	prostate:	n/a
48	chr4:148538521-148538571	GM12892	blood:	n/a
49	chr4:148538521-148538571	MCF10A-Er-Src	breast:	n/a
50	chr4:148538343-148538393	A549	lung:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:148544238..148546653-chr4:148547718..148550909,3	K562	blood:
2	chr4:148526097..148528506-chr4:148530218..148532114,2	K562	blood:
3	chr4:148541017..148543001-chr4:148604004..148606704,2	MCF-7	breast:
4	chr4:148554354..148557729-chr4:148560321..148563884,3	K562	blood:
5	chr4:148538536..148540743-chr4:148603744..148605353,2	MCF-7	breast:
6	chr4:148547064..148547916-chr4:148787644..148788200,2	MCF-7	breast:
7	chr4:148541060..148543503-chr4:148546785..148549015,2	MCF-7	breast:
8	chr4:148518441..148521336-chr4:148523862..148526303,2	K562	blood:
9	chr16:78160853..78161510-chr4:148527480..148528015,2	MCF-7	breast:
10	chr4:148538383..148539012-chrX:102942533..102943309,2	NB4	blood:
11	chr4:148531636..148535570-chr4:148536355..148539737,5	K562	blood:
12	chr4:148528379..148531648-chr4:148533404..148536404,5	MCF-7	breast:
13	chr4:148538481..148540071-chr4:148540760..148542427,2	MCF-7	breast:
14	chr4:148534491..148537230-chr4:148653257..148655916,2	MCF-7	breast:
15	chr4:148545096..148546653-chr4:148547913..148549905,2	K562	blood:
16	chr4:148537066..148539928-chr4:148545033..148546567,2	MCF-7	breast:
17	chr4:148542240..148544563-chr4:148545277..148546786,2	K562	blood:
18	chr4:148520672..148522853-chr4:148532687..148534632,2	K562	blood:
19	chr4:148541060..148543503-chr4:148546785..148549015,2	MCF-7	breast:
20	chr4:148550854..148553435-chr4:148554989..148557051,2	K562	blood:
21	chr4:148526097..148528506-chr4:148530218..148532114,2	K562	blood:
22	chr4:148550854..148553435-chr4:148554989..148557051,2	K562	blood:
23	chr4:148536735..148540067-chr4:148540690..148544003,4	MCF-7	breast:
24	chr4:148545096..148546653-chr4:148547913..148549905,2	K562	blood:
25	chr4:148533195..148535601-chr4:148603840..148606780,2	K562	blood:
26	chr4:148511550..148513191-chr4:148525701..148528628,2	K562	blood:
27	chr4:148533282..148535358-chr4:148536772..148538526,4	MCF-7	breast:
28	chr4:148528379..148531648-chr4:148533404..148536404,5	MCF-7	breast:
29	chr4:148567324..148568879-chr4:148605345..148606894,2	K562	blood:
30	chr4:148542240..148544563-chr4:148545277..148546786,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRMT10-1	chr4:148530703-148531112	XLOC_004115
2	lnc-PRMT10-1	chr4:148538239-148538396	XLOC_004115

No data

Variant related genes	Relation type
TMEM184C	TF binding region
PRMT10	TF binding region
ENSG00000251298	TF binding region
TMEM184C	CpG island
PRMT10	CpG island
ENSG00000251298	CpG island
ENSG00000164169	chromatin interactions
ENSG00000251298	chromatin interactions
ENSG00000164168	chromatin interactions
ENSG00000123562	chromatin interactions

Extended variants
information (count: 1681 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1681 , 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	rs2090424	chr4:148524852-148524853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561629895	chr4:148524857-148524858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530870732	chr4:148524860-148524861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189022553	chr4:148524876-148524877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563724447	chr4:148524941-148524942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545666424	chr4:148524950-148524951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142181900	chr4:148524951-148524952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151195004	chr4:148524965-148524966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181850231	chr4:148524966-148524967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187367243	chr4:148525003-148525004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190537524	chr4:148525018-148525019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35625830	chr4:148525062-148525063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140237181	chr4:148525119-148525120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150312815	chr4:148525129-148525130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537770186	chr4:148525140-148525141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556634944	chr4:148525168-148525169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373110137	chr4:148525181-148525182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539084436	chr4:148525183-148525184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576147846	chr4:148525201-148525202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552644909	chr4:148525239-148525240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34001293	chr4:148525248-148525249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs200362847	chr4:148525318-148525319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536372776	chr4:148525355-148525356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11932755	chr4:148525396-148525397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs376795345	chr4:148525546-148525547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575423579	chr4:148525596-148525597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182423896	chr4:148525600-148525601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555700692	chr4:148525603-148525604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11932883	chr4:148525677-148525678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532541762	chr4:148525684-148525685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552651865	chr4:148525706-148525707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36109476	chr4:148525752-148525753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111232259	chr4:148525822-148525823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115962052	chr4:148525882-148525883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185757952	chr4:148525896-148525897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548770202	chr4:148525908-148525909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189796558	chr4:148525918-148525919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141931067	chr4:148526003-148526004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551243778	chr4:148526008-148526009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571100930	chr4:148526009-148526010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182408234	chr4:148526011-148526012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377409778	chr4:148526012-148526013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370966811	chr4:148526070-148526071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185607482	chr4:148526071-148526072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145499145	chr4:148526073-148526074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374227346	chr4:148526082-148526083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147117887	chr4:148526130-148526131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535197817	chr4:148526151-148526152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74918895	chr4:148526160-148526161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75589646	chr4:148526164-148526165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	20952505	CNVD

Chromatin state (count:1780 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148519200-148538000	Weak transcription	Aorta	Aorta
2	chr4:148521400-148526800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:148521400-148538000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:148521600-148526800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:148521600-148531400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:148522000-148526200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:148522000-148526800	Weak transcription	Osteobl	bone
8	chr4:148525800-148526400	Enhancers	Stomach Smooth Muscle	stomach
9	chr4:148526200-148527200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:148526200-148527200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:148526800-148527000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:148526800-148527000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:148526800-148527200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:148526800-148527200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:148526800-148527200	Enhancers	Osteobl	bone
16	chr4:148527000-148537600	Weak transcription	Brain Anterior Caudate	brain
17	chr4:148527200-148531200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:148527200-148531600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:148527200-148538000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:148528200-148529600	Enhancers	HepG2	liver
21	chr4:148528400-148529400	Enhancers	Fetal Intestine Large	intestine
22	chr4:148528600-148529800	Enhancers	Fetal Intestine Small	intestine
23	chr4:148529600-148537600	Weak transcription	HepG2	liver
24	chr4:148531200-148532200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:148531400-148532400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:148531400-148532600	Enhancers	NHDF-Ad	bronchial
27	chr4:148531400-148532800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:148531600-148532600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:148531800-148532200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:148532600-148537600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:148532800-148538000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:148533600-148534000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:148534000-148537600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr4:148535200-148535400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:148535200-148535400	Enhancers	Pancreas	Pancrea
36	chr4:148535400-148537400	Weak transcription	Pancreas	Pancrea
37	chr4:148535400-148538200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:148537200-148539800	Active TSS	H1 Cell Line	embryonic stem cell
39	chr4:148537400-148537600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:148537400-148537600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:148537400-148537600	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr4:148537400-148537600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:148537400-148537600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr4:148537400-148537600	Enhancers	Fetal Heart	heart
45	chr4:148537400-148537600	Enhancers	Pancreas	Pancrea
46	chr4:148537400-148537600	Active TSS	GM12878-XiMat	blood
47	chr4:148537400-148537600	Active TSS	Hela-S3	cervix
48	chr4:148537400-148537800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:148537400-148537800	Enhancers	A549	lung
50	chr4:148537400-148538000	Enhancers	Fetal Intestine Small	intestine

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