Variant report

Variant	nsv1031814
Chromosome Location	chr4:186986315-187052824
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	chr4:186989219-186989538	HepG2	liver:	n/a	n/a
2	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
3	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
7	CBX3	chr4:186989030-186989622	HCT-116	colon:	n/a	chr4:186989176-186989187
8	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
9	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
10	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
11	CEBPB	chr4:186990084-186990532	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
13	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
14	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
15	CEBPB	chr4:187009826-187010155	HepG2	liver:	n/a	chr4:187009905-187009916
16	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
17	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
18	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
19	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
20	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
21	CHD1	chr4:187026105-187026212	H1-hESC	embryonic stem cell:	n/a	chr4:187026142-187026152
22	CHD2	chr4:187000118-187000352	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:187002365-187002951	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr4:187025588-187026455	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:187021070-187021161	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:186989260-186989410	AG04449	skin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
27	CTCF	chr4:187021040-187021190	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr4:187026080-187026230	GM12873	blood:	n/a	n/a
29	CTCF	chr4:186989320-186989470	GM06990	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
30	CTCF	chr4:187026160-187026310	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr4:187026160-187026310	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr4:186989280-186989430	HFF-Myc	foreskin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
33	CTCF	chr4:186989087-186989592	MCF-7	breast:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
34	CTCF	chr4:186989260-186989410	HL-60	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
35	CTCF	chr4:186989240-186989390	HRE	kidney:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
36	CTCF	chr4:186989232-186989458	Medullo	brain:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
37	CTCF	chr4:186988960-186989110	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr4:186989242-186989372	SK-N-SH_RA	brain:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
39	CTCF	chr4:186989240-186989390	RPTEC	kidney:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
40	CTCF	chr4:186989280-186989430	HBMEC	blood vessel:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
41	CTCF	chr4:187018397-187018436	GM12878	blood:	n/a	n/a
42	CTCF	chr4:186989300-186989450	GM12864	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
43	CTCF	chr4:187026260-187026410	GM12871	blood:	n/a	n/a
44	CTCF	chr4:186989280-186989430	AG04450	lung:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
45	CTCF	chr4:186989260-186989410	HA-sp	spinal cord:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
46	CTCF	chr4:186989260-186989410	HEK293	kidney:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
47	CTCF	chr4:187021020-187021170	A549	lung:	n/a	n/a
48	CTCF	chr4:187026241-187026318	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:187021065-187021164	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr4:186989280-186989430	AG09309	skin:	n/a	chr4:186989349-186989365 chr4:186989348-186989366 chr4:186989351-186989364 chr4:186989350-186989371

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187000846-187000896	GM19239	blood:	n/a
2	chr4:187039516-187039566	H1-hESC	embryonic stem cell:	embryo
3	chr4:187026710-187026760	HRPEpiC	eye:	n/a
4	chr4:187037256-187037306	HCF	heart:	n/a
5	chr4:187025886-187025936	Hepatocyte	liver:	n/a
6	chr4:187000846-187000896	GM19239	blood:	n/a
7	chr4:187039516-187039566	H1-hESC	embryonic stem cell:	embryo
8	chr4:187026710-187026760	HRPEpiC	eye:	n/a
9	chr4:187037256-187037306	HCF	heart:	n/a
10	chr4:187025886-187025936	Hepatocyte	liver:	n/a
11	chr4:186990324-186990374	CMK	blood:	n/a
12	chr4:187025654-187025704	SK-N-SH_RA	brain:	n/a
13	chr4:187026710-187026760	HCT-116	colon:	n/a
14	chr4:187002617-187002667	GM19239	blood:	n/a
15	chr4:187025886-187025936	CMK	blood:	n/a
16	chr4:186990425-186990475	ProgFib	skin:	n/a
17	chr4:187025886-187025936	RPTEC	kidney:	n/a
18	chr4:186990202-186990252	PANC-1	pancreas:	n/a
19	chr4:187013645-187013695	HRPEpiC	eye:	n/a
20	chr4:187003000-187003050	NT2-D1	testis:	n/a
21	chr4:187000846-187000896	MCF10A-Er-Src	breast:	n/a
22	chr4:187037318-187037368	GM12891	blood:	n/a
23	chr4:186990315-186990365	HEEpiC	esophagus:	n/a
24	chr4:187013645-187013695	HMEC	breast:	n/a
25	chr4:187026970-187027020	HUVEC	blood vessel:	n/a
26	chr4:187026970-187027020	MCF-7	breast:	n/a
27	chr4:187003000-187003050	HEEpiC	esophagus:	n/a
28	chr4:187037318-187037368	AG09309	skin:	n/a
29	chr4:187025886-187025936	HepG2	liver:	n/a
30	chr4:187013645-187013695	NH-A	brain:	n/a
31	chr4:187013536-187013586	HAEpiC	amniotic membrane:	n/a
32	chr4:186990315-186990365	RPTEC	kidney:	n/a
33	chr4:187039516-187039566	PANC-1	pancreas:	n/a
34	chr4:187025420-187025470	HCM	heart:	n/a
35	chr4:186990425-186990475	HepG2	liver:	n/a
36	chr4:186990315-186990365	ovcar-3	ovarian:	n/a
37	chr4:187037256-187037306	HepG2	liver:	n/a
38	chr4:187003000-187003050	HL-60	blood:	n/a
39	chr4:187026225-187026275	HCF	heart:	n/a
40	chr4:187039516-187039566	HCF	heart:	n/a
41	chr4:187026225-187026275	ProgFib	skin:	n/a
42	chr4:186990202-186990252	LNCaP	prostate:	n/a
43	chr4:186990315-186990365	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:187037318-187037368	ProgFib	skin:	n/a
45	chr4:187013536-187013586	Hepatocyte	liver:	n/a
46	chr4:187026278-187026328	NB4	blood:	n/a
47	chr4:187025654-187025704	HCT-116	colon:	n/a
48	chr4:187026970-187027020	IMR90	lung:	fetal
49	chr4:187013645-187013695	GM12891	blood:	n/a
50	chr4:187037318-187037368	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
2	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
3	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
4	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
5	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
6	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
7	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
8	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
9	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
10	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
11	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
12	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
13	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
14	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
15	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
16	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253013	TF binding region
FAM149A	TF binding region
TLR3	TF binding region
ENSG00000253013	CpG island
FAM149A	CpG island
TLR3	CpG island
ENSG00000145476	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000204424	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000250641	chromatin interactions

Extended variants
information (count: 2815 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2815 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148981645	chr4:186986474-186986475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77676537	chr4:186986497-186986498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573544413	chr4:186986510-186986511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547603514	chr4:186986528-186986529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145550908	chr4:186986542-186986543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184308476	chr4:186986609-186986610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4862632	chr4:186986617-186986618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189640879	chr4:186986628-186986629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561428319	chr4:186986657-186986658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs36035924	chr4:186986687-186986688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181194157	chr4:186986787-186986788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186702576	chr4:186986826-186986827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373716575	chr4:186986841-186986842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147754271	chr4:186986869-186986870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188595407	chr4:186986896-186986897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571395417	chr4:186986925-186986926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs66818138	chr4:186986933-186986934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142617987	chr4:186986967-186986968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371631871	chr4:186986968-186986969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567340131	chr4:186986973-186986974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112330519	chr4:186986986-186986987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181434088	chr4:186987013-186987014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552975081	chr4:186987051-186987052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567173655	chr4:186987073-186987074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539298484	chr4:186987074-186987075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146896722	chr4:186987085-186987086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535094680	chr4:186987086-186987087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575791718	chr4:186987106-186987107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544767455	chr4:186987179-186987180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115686367	chr4:186987263-186987264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534727432	chr4:186987280-186987281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185889291	chr4:186987296-186987297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148303390	chr4:186987365-186987366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540237014	chr4:186987372-186987373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560076951	chr4:186987401-186987402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546908163	chr4:186987433-186987434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532364888	chr4:186987458-186987459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140425174	chr4:186987535-186987536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150430611	chr4:186987537-186987538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138215534	chr4:186987544-186987545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538997520	chr4:186987545-186987546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190745181	chr4:186987555-186987556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567272833	chr4:186987581-186987582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367713864	chr4:186987594-186987595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201651940	chr4:186987602-186987603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546627675	chr4:186987610-186987611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554388826	chr4:186987613-186987614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142607029	chr4:186987617-186987618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184219312	chr4:186987623-186987624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145994236	chr4:186987631-186987632	Enhancers Weak 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:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186980200-186989200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr4:186985000-186989000	Weak transcription	Left Ventricle	heart
3	chr4:186986800-186987000	Enhancers	HepG2	liver
4	chr4:186987200-186987400	Enhancers	Brain Hippocampus Middle	brain
5	chr4:186987200-186988200	Enhancers	Brain Germinal Matrix	brain
6	chr4:186987200-186988800	Weak transcription	HepG2	liver
7	chr4:186987400-186989000	Weak transcription	Brain Hippocampus Middle	brain
8	chr4:186988200-186989400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:186988200-186989800	Weak transcription	Brain Germinal Matrix	brain
10	chr4:186988400-186988800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:186988400-186989200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:186988800-186989000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:186988800-186989000	Enhancers	Colon Smooth Muscle	Colon
14	chr4:186988800-186989200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:186988800-186989200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:186988800-186989200	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr4:186988800-186989200	Enhancers	HepG2	liver
18	chr4:186988800-186989200	Enhancers	NHDF-Ad	bronchial
19	chr4:186988800-186989400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr4:186988800-186989400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:186989000-186989200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:186989000-186989200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr4:186989000-186989200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
24	chr4:186989000-186989200	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr4:186989000-186989200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:186989000-186989200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:186989000-186989200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:186989000-186989200	Enhancers	Fetal Kidney	kidney
29	chr4:186989000-186989200	Enhancers	Fetal Lung	lung
30	chr4:186989000-186989200	Enhancers	Ovary	ovary
31	chr4:186989000-186989200	Enhancers	Pancreas	Pancrea
32	chr4:186989000-186989200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr4:186989000-186989200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr4:186989000-186989200	Enhancers	Spleen	Spleen
35	chr4:186989000-186989200	Enhancers	Dnd41	blood
36	chr4:186989000-186989200	Bivalent Enhancer	GM12878-XiMat	blood
37	chr4:186989000-186989200	Enhancers	Osteobl	bone
38	chr4:186989000-186989400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:186989000-186989400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr4:186989000-186989400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr4:186989000-186989400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:186989000-186989400	Enhancers	Liver	Liver
43	chr4:186989000-186989400	Flanking Active TSS	Brain Hippocampus Middle	brain
44	chr4:186989000-186989400	Enhancers	Brain Substantia Nigra	brain
45	chr4:186989000-186989400	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr4:186989000-186989400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:186989000-186989400	Enhancers	Fetal Muscle Leg	muscle
48	chr4:186989000-186989400	Enhancers	Fetal Stomach	stomach
49	chr4:186989000-186989400	Enhancers	Left Ventricle	heart
50	chr4:186989000-186989400	Enhancers	Right Ventricle	heart

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