Variant report

Variant	nsv964737
Chromosome Location	chr4:8467874-8473530
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	chr4:8470490-8470763	K562	blood:	n/a	n/a
2	BACH1	chr4:8470514-8470604	K562	blood:	n/a	n/a
3	BACH1	chr4:8470623-8470714	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:8470370-8470766	K562	blood:	n/a	n/a
5	BHLHE40	chr4:8470457-8470808	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:8470496-8470696	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:8470534-8470889	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr4:8470628-8470762	HepG2	liver:	n/a	n/a
9	CCNT2	chr4:8471937-8471988	K562	blood:	n/a	n/a
10	CEBPB	chr4:8470414-8470764	K562	blood:	n/a	chr4:8470425-8470437
11	CEBPB	chr4:8470422-8470760	MCF-7	breast:	n/a	chr4:8470425-8470437
12	CEBPB	chr4:8470472-8470730	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:8470417-8470839	H1-hESC	embryonic stem cell:	n/a	chr4:8470425-8470437
14	CHD2	chr4:8473428-8473447	K562	blood:	n/a	n/a
15	CHD2	chr4:8470544-8470795	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:8470550-8470806	GM12878	blood:	n/a	n/a
17	CTCF	chr4:8470508-8470814	A549	lung:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
18	CTCF	chr4:8470580-8470730	AG04450	lung:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
19	CTCF	chr4:8470580-8470730	HEEpiC	esophagus:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
20	CTCF	chr4:8470513-8470784	GM10248	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
21	CTCF	chr4:8470513-8470801	H1-hESC	embryonic stem cell:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
22	CTCF	chr4:8470040-8470190	GM12873	blood:	n/a	n/a
23	CTCF	chr4:8470900-8471050	GM12870	blood:	n/a	n/a
24	CTCF	chr4:8470600-8470750	GM12864	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
25	CTCF	chr4:8470372-8471011	K562	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
26	CTCF	chr4:8470580-8470730	GM12869	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
27	CTCF	chr4:8470580-8470730	AG09309	skin:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
28	CTCF	chr4:8470292-8470413	GM13976	blood:	n/a	n/a
29	CTCF	chr4:8470514-8470770	GM13976	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
30	CTCF	chr4:8470481-8470764	ECC-1	luminal epithelium:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
31	CTCF	chr4:8470580-8470730	MCF-7	breast:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
32	CTCF	chr4:8470600-8470750	HRPEpiC	eye:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
33	CTCF	chr4:8470445-8470817	T-47D	breast:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
34	CTCF	chr4:8470506-8470798	K562	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
35	CTCF	chr4:8470460-8470730	HAc	cerebellar:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
36	CTCF	chr4:8470580-8470730	HEK293	kidney:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
37	CTCF	chr4:8470489-8470495	Lung_OC	lung:	n/a	n/a
38	CTCF	chr4:8470580-8470730	HRE	kidney:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
39	CTCF	chr4:8471400-8471550	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr4:8470511-8470816	LNCaP	prostate:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
41	CTCF	chr4:8470580-8470730	HCFaa	heart:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
42	CTCF	chr4:8470600-8470750	WI-38	lung:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
43	CTCF	chr4:8470600-8470750	GM12871	blood:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
44	CTCF	chr4:8470501-8470753	HepG2	liver:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
45	CTCF	chr4:8470388-8471022	HCT-116	colon:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
46	CTCF	chr4:8470560-8470710	HepG2	liver:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
47	CTCF	chr4:8470120-8470144	GM20000	blood:	n/a	n/a
48	CTCF	chr4:8470560-8470710	HEEpiC	esophagus:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
49	CTCF	chr4:8470428-8470779	H1-hESC	embryonic stem cell:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678
50	CTCF	chr4:8470480-8470891	H1-hESC	embryonic stem cell:	n/a	chr4:8470658-8470671 chr4:8470655-8470673 chr4:8470657-8470678

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8472850-8472900	HL-60	blood:	n/a
2	chr4:8472938-8472988	NHBE	bronchial:	n/a
3	chr4:8468476-8468526	ovcar-3	ovarian:	n/a
4	chr4:8468878-8468928	SKMC	muscle:	n/a
5	chr4:8468179-8468229	HepG2	liver:	n/a
6	chr4:8468476-8468526	AoSMC	blood vessel:	n/a
7	chr4:8473113-8473163	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:8468179-8468229	GM19239	blood:	n/a
9	chr4:8473051-8473101	ProgFib	skin:	n/a
10	chr4:8473113-8473163	Jurkat	blood:	n/a
11	chr4:8472850-8472900	HIPEpiC	eye:	n/a
12	chr4:8468476-8468526	HCT-116	colon:	n/a
13	chr4:8473113-8473163	BJ	skin:	n/a
14	chr4:8469051-8469101	U87	brain:	n/a
15	chr4:8468310-8468360	PrEC	prostate:	n/a
16	chr4:8468878-8468928	HCPEpiC	choroid plexus:	n/a
17	chr4:8473051-8473101	BE2_C	brain:	n/a
18	chr4:8468476-8468526	AG04450	lung:	fetal
19	chr4:8473051-8473101	GM06990	blood:	n/a
20	chr4:8472938-8472988	GM19239	blood:	n/a
21	chr4:8469051-8469101	BJ	skin:	n/a
22	chr4:8473051-8473101	GM12891	blood:	n/a
23	chr4:8473113-8473163	SKMC	muscle:	n/a
24	chr4:8468878-8468928	Caco-2	colon:	n/a
25	chr4:8468476-8468526	AG09319	gingival:	n/a
26	chr4:8473113-8473163	LNCaP	prostate:	n/a
27	chr4:8473051-8473101	AoSMC	blood vessel:	n/a
28	chr4:8472895-8472945	HIPEpiC	eye:	n/a
29	chr4:8473051-8473101	MCF10A-Er-Src	breast:	n/a
30	chr4:8473113-8473163	NH-A	brain:	n/a
31	chr4:8468878-8468928	ProgFib	skin:	n/a
32	chr4:8472895-8472945	ProgFib	skin:	n/a
33	chr4:8468476-8468526	SK-N-MC	brain:	n/a
34	chr4:8468476-8468526	HIPEpiC	eye:	n/a
35	chr4:8468310-8468360	BE2_C	brain:	n/a
36	chr4:8473051-8473101	NHBE	bronchial:	n/a
37	chr4:8468476-8468526	HRCEpiC	kidney:	n/a
38	chr4:8473051-8473101	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:8472850-8472900	GM06990	blood:	n/a
40	chr4:8472895-8472945	NH-A	brain:	n/a
41	chr4:8473113-8473163	GM12891	blood:	n/a
42	chr4:8468878-8468928	GM12891	blood:	n/a
43	chr4:8472938-8472988	U87	brain:	n/a
44	chr4:8472938-8472988	AG09309	skin:	n/a
45	chr4:8468179-8468229	HCF	heart:	n/a
46	chr4:8468476-8468526	H1-hESC	embryonic stem cell:	embryo
47	chr4:8473113-8473163	HEEpiC	esophagus:	n/a
48	chr4:8473113-8473163	U87	brain:	n/a
49	chr4:8472850-8472900	HUVEC	blood vessel:	n/a
50	chr4:8472895-8472945	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8466177..8468891-chr4:8548337..8550041,2	MCF-7	breast:
2	chr4:8470159..8471594-chr4:8587070..8589399,12	MCF-7	breast:
3	chr4:8470474..8471083-chr4:8586784..8587611,2	MCF-7	breast:
4	chr4:8469176..8470794-chr4:8477101..8479273,2	MCF-7	breast:
5	chr4:8470225..8471528-chr4:8595848..8597093,11	K562	blood:
6	chr4:8459420..8461262-chr4:8464896..8467883,3	K562	blood:
7	chr4:8468812..8470313-chr4:8589998..8592913,2	K562	blood:
8	chr4:8473000..8473785-chr4:8548526..8549174,2	MCF-7	breast:
9	chr4:8471024..8473735-chr4:8474244..8476611,2	K562	blood:
10	chr4:8468552..8470312-chr4:8591413..8592935,2	K562	blood:
11	chr4:8243625..8244519-chr4:8470569..8471144,2	MCF-7	breast:
12	chr4:8470170..8471110-chr4:8595421..8596838,7	MCF-7	breast:
13	chr4:8472049..8473735-chr4:8474244..8476711,2	K562	blood:
14	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
15	chr4:8469952..8472230-chr4:8539162..8541122,2	MCF-7	breast:
16	chr4:8473110..8474734-chr4:8594190..8596233,2	MCF-7	breast:
17	chr4:8441944..8444438-chr4:8468508..8471362,2	K562	blood:
18	chr4:8470194..8471378-chr4:8548265..8549392,10	MCF-7	breast:
19	chr4:8470409..8471154-chr4:8548815..8549418,2	MCF-7	breast:
20	chr4:8470336..8471339-chr4:8588024..8588933,6	MCF-7	breast:
21	chr4:8470272..8471640-chr4:8595955..8596822,5	MCF-7	breast:
22	chr4:8470834..8472351-chr4:8587366..8589099,2	MCF-7	breast:
23	chr4:8451706..8454826-chr4:8468396..8471846,3	K562	blood:

Variant related genes	Relation type
TRMT44	TF binding region
TRMT44	CpG island
ENSG00000087008	chromatin interactions
ENSG00000109625	chromatin interactions
ENSG00000155275	chromatin interactions

Extended variants
information (count: 354 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386671372	chr4:8467883-8467884	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs73213423	chr4:8467884-8467885	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs111457315	chr4:8467887-8467888	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555753132	chr4:8467895-8467896	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs142657876	chr4:8467917-8467918	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs538226161	chr4:8467946-8467947	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs556722277	chr4:8467953-8467954	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs374753710	chr4:8467984-8467985	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377293463	chr4:8467996-8467997	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116302629	chr4:8468006-8468007	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs115369283	chr4:8468033-8468034	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112791693	chr4:8468069-8468070	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573115424	chr4:8468127-8468128	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs540123070	chr4:8468155-8468156	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562003231	chr4:8468162-8468163	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs372476850	chr4:8468169-8468170	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528887970	chr4:8468194-8468195	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs146732323	chr4:8468202-8468203	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs554606815	chr4:8468203-8468204	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs184578361	chr4:8468214-8468215	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs73213424	chr4:8468223-8468224	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs566926152	chr4:8468272-8468273	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs16842333	chr4:8468295-8468296	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549446992	chr4:8468302-8468303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77254399	chr4:8468305-8468306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139284276	chr4:8468306-8468307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371772309	chr4:8468310-8468311	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs562138196	chr4:8468314-8468315	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs577688144	chr4:8468351-8468352	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs545105411	chr4:8468417-8468418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556556931	chr4:8468434-8468435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560076789	chr4:8468466-8468467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574028951	chr4:8468475-8468476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150367038	chr4:8468478-8468479	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs375096829	chr4:8468527-8468528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539105676	chr4:8468549-8468550	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35120669	chr4:8468568-8468569	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529424445	chr4:8468594-8468595	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557946560	chr4:8468624-8468625	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201415281	chr4:8468636-8468637	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150311035	chr4:8468637-8468638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs369164688	chr4:8468667-8468668	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs559125762	chr4:8468705-8468706	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190734479	chr4:8468731-8468732	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181489812	chr4:8468750-8468751	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187015457	chr4:8468806-8468807	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190156753	chr4:8468825-8468826	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77743832	chr4:8468888-8468889	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374980227	chr4:8468894-8468895	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs560178232	chr4:8468969-8468970	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8446400-8473800	Strong transcription	Fetal Stomach	stomach
2	chr4:8446600-8473400	Strong transcription	Dnd41	blood
3	chr4:8446600-8474000	Strong transcription	Fetal Muscle Leg	muscle
4	chr4:8447000-8474400	Strong transcription	Fetal Brain Female	brain
5	chr4:8447000-8475200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:8447000-8480200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:8447200-8473000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:8447200-8480200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr4:8447400-8474000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:8447400-8482200	Strong transcription	Primary T cells from cord blood	blood
11	chr4:8447600-8472200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr4:8447600-8473400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr4:8447800-8472800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:8451200-8473600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:8456000-8469800	Weak transcription	Stomach Mucosa	stomach
16	chr4:8456800-8468600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr4:8457200-8470600	Strong transcription	Fetal Muscle Trunk	muscle
18	chr4:8457800-8470800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr4:8458200-8472000	Weak transcription	Fetal Heart	heart
20	chr4:8459400-8474000	Strong transcription	Fetal Intestine Small	intestine
21	chr4:8459600-8470000	Weak transcription	Fetal Brain Male	brain
22	chr4:8459800-8478800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr4:8460000-8470000	Weak transcription	K562	blood
24	chr4:8460200-8469000	Weak transcription	Small Intestine	intestine
25	chr4:8460200-8470800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:8462400-8472800	Strong transcription	Liver	Liver
27	chr4:8463000-8470600	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr4:8463000-8471600	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr4:8463400-8473800	Weak transcription	Fetal Kidney	kidney
30	chr4:8463600-8469800	Weak transcription	NHDF-Ad	bronchial
31	chr4:8463800-8478800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr4:8464200-8471200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr4:8464400-8471200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr4:8464600-8473200	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr4:8464600-8474000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:8464800-8468000	Strong transcription	Primary B cells from cord blood	blood
37	chr4:8464800-8468800	Strong transcription	HSMMtube	muscle
38	chr4:8464800-8472000	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr4:8464800-8472000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr4:8464800-8473400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr4:8464800-8473600	Strong transcription	Brain Angular Gyrus	brain
42	chr4:8465000-8468000	Strong transcription	HepG2	liver
43	chr4:8465000-8468600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:8465000-8471400	Strong transcription	Left Ventricle	heart
45	chr4:8465200-8468000	Strong transcription	NH-A	brain
46	chr4:8465200-8468200	Genic enhancers	Placenta	Placenta
47	chr4:8465200-8470400	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr4:8465200-8470600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:8465200-8470800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr4:8465200-8471400	Strong transcription	Primary B cells from peripheral blood	blood

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