Variant report

Variant	nsv537432
Chromosome Location	chr4:187004240-187073316
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	ARID3A	chr4:187058552-187058902	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187058644-187058864	K562	blood:	n/a	n/a
3	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
4	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:187071057-187071421	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
7	BACH1	chr4:187066156-187066584	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:187058431-187058728	GM12878	blood:	n/a	n/a
11	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
12	BATF	chr4:187058420-187058694	GM12878	blood:	n/a	n/a
13	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
15	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
16	BCL3	chr4:187059720-187060074	GM12878	blood:	n/a	n/a
17	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
20	BHLHE40	chr4:187055496-187055825	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:187059455-187059456	GM12878	blood:	n/a	n/a
22	CEBPB	chr4:187037849-187038207	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
23	CEBPB	chr4:187058612-187058894	A549	lung:	n/a	n/a
24	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
25	CEBPB	chr4:187067232-187067556	H1-hESC	embryonic stem cell:	n/a	chr4:187067399-187067412
26	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
27	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
28	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
29	CEBPB	chr4:187037874-187038237	H1-hESC	embryonic stem cell:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
30	CEBPB	chr4:187058752-187058939	K562	blood:	n/a	n/a
31	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
32	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
33	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
34	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
35	CEBPB	chr4:187059932-187059959	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:187037847-187038225	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
37	CEBPB	chr4:187009826-187010155	HepG2	liver:	n/a	chr4:187009905-187009916
38	CHD1	chr4:187059861-187059865	GM12878	blood:	n/a	n/a
39	CHD1	chr4:187026105-187026212	H1-hESC	embryonic stem cell:	n/a	chr4:187026142-187026152
40	CHD2	chr4:187055449-187055790	GM12878	blood:	n/a	n/a
41	CHD2	chr4:187071137-187071471	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTBP2	chr4:187065194-187065977	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr4:187025588-187026455	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:187065420-187065570	HCM	heart:	n/a	n/a
45	CTCF	chr4:187071215-187071344	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:187065380-187065530	GM12873	blood:	n/a	n/a
47	CTCF	chr4:187018397-187018436	GM12878	blood:	n/a	n/a
48	CTCF	chr4:187071220-187071370	GM12867	blood:	n/a	n/a
49	CTCF	chr4:187065440-187065590	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr4:187054060-187054210	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187065713-187065763	AG04449	skin:	fetal
2	chr4:187065831-187065881	T-47D	breast:	n/a
3	chr4:187065831-187065881	SAEC	small airway:	n/a
4	chr4:187065713-187065763	AG04449	skin:	fetal
5	chr4:187065831-187065881	T-47D	breast:	n/a
6	chr4:187065831-187065881	SAEC	small airway:	n/a
7	chr4:187063756-187063806	ovcar-3	ovarian:	n/a
8	chr4:187026710-187026760	GM12878	blood:	n/a
9	chr4:187053574-187053624	PrEC	prostate:	n/a
10	chr4:187026225-187026275	LNCaP	prostate:	n/a
11	chr4:187065516-187065566	AG04449	skin:	fetal
12	chr4:187066430-187066480	HEK293	kidney:	embryo
13	chr4:187071162-187071212	HMEC	breast:	n/a
14	chr4:187037256-187037306	NHDF-neo	bronchial:	n/a
15	chr4:187053574-187053624	NT2-D1	testis:	n/a
16	chr4:187066430-187066480	HEEpiC	esophagus:	n/a
17	chr4:187066505-187066555	HRPEpiC	eye:	n/a
18	chr4:187065417-187065467	GM12891	blood:	n/a
19	chr4:187037256-187037306	SK-N-SH_RA	brain:	n/a
20	chr4:187023193-187023243	LNCaP	prostate:	n/a
21	chr4:187065713-187065763	AG10803	skin:	n/a
22	chr4:187069057-187069107	HEEpiC	esophagus:	n/a
23	chr4:187065516-187065566	GM12891	blood:	n/a
24	chr4:187066279-187066329	NT2-D1	testis:	n/a
25	chr4:187066430-187066480	MCF-7	breast:	n/a
26	chr4:187063756-187063806	SK-N-SH_RA	brain:	n/a
27	chr4:187026710-187026760	NH-A	brain:	n/a
28	chr4:187069057-187069107	Caco-2	colon:	n/a
29	chr4:187025654-187025704	BE2_C	brain:	n/a
30	chr4:187066279-187066329	HRCEpiC	kidney:	n/a
31	chr4:187066279-187066329	IMR90	lung:	fetal
32	chr4:187065955-187066005	K562	blood:	n/a
33	chr4:187065846-187065896	GM12892	blood:	n/a
34	chr4:187025654-187025704	HRCEpiC	kidney:	n/a
35	chr4:187023193-187023243	NHBE	bronchial:	n/a
36	chr4:187070303-187070353	T-47D	breast:	n/a
37	chr4:187025654-187025704	T-47D	breast:	n/a
38	chr4:187025420-187025470	PFSK-1	brain:	n/a
39	chr4:187065713-187065763	CMK	blood:	n/a
40	chr4:187025886-187025936	HCPEpiC	choroid plexus:	n/a
41	chr4:187065950-187066000	RPTEC	kidney:	n/a
42	chr4:187070357-187070407	IMR90	lung:	fetal
43	chr4:187053574-187053624	HRPEpiC	eye:	n/a
44	chr4:187026970-187027020	HCM	heart:	n/a
45	chr4:187065940-187065990	AG09309	skin:	n/a
46	chr4:187065846-187065896	GM12891	blood:	n/a
47	chr4:187037256-187037306	A549	lung:	n/a
48	chr4:187013536-187013586	HepG2	liver:	n/a
49	chr4:187026710-187026760	HEEpiC	esophagus:	n/a
50	chr4:187037256-187037306	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
2	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
3	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
4	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
5	chr4:187061612..187063617-chr4:187065011..187066705,2	K562	blood:
6	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
7	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
8	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
9	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
10	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
11	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
12	chr4:186953201..186953720-chr4:187058277..187058867,2	MCF-7	breast:
13	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
14	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
15	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
16	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
17	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
18	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
19	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
20	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
21	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
22	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253013	TF binding region
FAM149A	TF binding region
ENSG00000253013	CpG island
FAM149A	CpG island
ENSG00000109794	chromatin interactions
ENSG00000250641	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000204424	chromatin interactions
ENSG00000145476	chromatin interactions

Extended variants
information (count: 2901 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2901 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113275119	chr4:187004243-187004244	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs201792200	chr4:187004327-187004328	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs369886993	chr4:187004329-187004330	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs199658443	chr4:187004357-187004358	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs202066722	chr4:187004368-187004369	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs373400665	chr4:187004411-187004412	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs532943362	chr4:187004418-187004419	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs201222071	chr4:187004425-187004426	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs112666655	chr4:187004474-187004475	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs147873871	chr4:187004484-187004485	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs121434431	chr4:187004500-187004501	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs35617964	chr4:187004517-187004518	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145252794	chr4:187004521-187004522	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs571300094	chr4:187004523-187004524	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs149184129	chr4:187004524-187004525	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs143330461	chr4:187004538-187004539	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs35111588	chr4:187004544-187004545	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs140712645	chr4:187004556-187004557	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs376735334	chr4:187004565-187004566	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs368882892	chr4:187004587-187004588	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs372569709	chr4:187004595-187004596	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs192543136	chr4:187004610-187004611	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184426724	chr4:187004614-187004615	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200785357	chr4:187004619-187004620	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34597061	chr4:187004633-187004634	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114810441	chr4:187004673-187004674	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189369369	chr4:187004685-187004686	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372944756	chr4:187004721-187004722	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201698078	chr4:187004727-187004728	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145921610	chr4:187004730-187004731	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574038103	chr4:187004751-187004752	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138505418	chr4:187004761-187004762	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73025939	chr4:187004767-187004768	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150315296	chr4:187004768-187004769	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137992614	chr4:187004798-187004799	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371265702	chr4:187004815-187004816	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149490656	chr4:187004826-187004827	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376729108	chr4:187004839-187004840	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144019953	chr4:187004851-187004852	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78758719	chr4:187004855-187004856	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199543128	chr4:187004904-187004905	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540959112	chr4:187004908-187004909	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371358596	chr4:187004969-187004970	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374422592	chr4:187005012-187005013	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377509605	chr4:187005020-187005021	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs5743318	chr4:187005049-187005050	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116269970	chr4:187005057-187005058	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147431766	chr4:187005064-187005065	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142813217	chr4:187005131-187005132	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370090850	chr4:187005168-187005169	Enhancers Weak transcription Strong transcription	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
Metanephric adenoma	20802469	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
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186990600-187006200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:186990600-187006200	Weak transcription	Small Intestine	intestine
3	chr4:186991000-187006200	Weak transcription	Colonic Mucosa	Colon
4	chr4:186991200-187005600	Weak transcription	Right Ventricle	heart
5	chr4:186991200-187007600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:186991200-187009200	Weak transcription	Lung	lung
7	chr4:186991200-187009400	Weak transcription	Brain Anterior Caudate	brain
8	chr4:186991200-187009600	Weak transcription	Fetal Kidney	kidney
9	chr4:186995600-187006400	Weak transcription	Colon Smooth Muscle	Colon
10	chr4:186995800-187009200	Weak transcription	Pancreas	Pancrea
11	chr4:187000600-187005800	Weak transcription	Left Ventricle	heart
12	chr4:187000800-187006200	Weak transcription	Spleen	Spleen
13	chr4:187000800-187006600	Weak transcription	Fetal Stomach	stomach
14	chr4:187001000-187008000	Weak transcription	Ovary	ovary
15	chr4:187001000-187018200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr4:187001200-187006000	Weak transcription	Esophagus	oesophagus
17	chr4:187001200-187017200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr4:187001400-187004600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:187001600-187009000	Weak transcription	Brain Substantia Nigra	brain
20	chr4:187002400-187004600	Strong transcription	Liver	Liver
21	chr4:187002400-187005400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:187002600-187004800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:187002600-187013400	Weak transcription	Psoas Muscle	Psoas
24	chr4:187002800-187006200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr4:187002800-187009600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:187003000-187008200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr4:187003600-187004600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:187003600-187004600	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr4:187003600-187005400	Strong transcription	Placenta	Placenta
30	chr4:187003800-187004600	Strong transcription	Primary hematopoietic stem cells	blood
31	chr4:187003800-187005000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:187003800-187005000	Strong transcription	Adipose Nuclei	Adipose
33	chr4:187003800-187009600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr4:187004000-187004800	Strong transcription	Duodenum Mucosa	Duodenum
35	chr4:187004000-187005000	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr4:187004200-187004600	ZNF genes & repeats	Aorta	Aorta
37	chr4:187004200-187005000	Strong transcription	Fetal Lung	lung
38	chr4:187004600-187005200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:187004600-187005200	Weak transcription	Aorta	Aorta
40	chr4:187004600-187006400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr4:187004600-187007400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr4:187004600-187009600	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr4:187004600-187010600	Weak transcription	Liver	Liver
44	chr4:187004800-187006800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:187004800-187015800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr4:187005000-187006800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr4:187005000-187007000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:187005000-187009200	Weak transcription	Adipose Nuclei	Adipose
49	chr4:187005000-187010400	Weak transcription	Fetal Lung	lung
50	chr4:187005400-187011000	Weak transcription	Placenta	Placenta

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