Variant report

Variant	nsv878548
Chromosome Location	chr4:7295154-7333152
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	ATF3	chr4:7325569-7325906	A549	lung:	n/a	n/a
2	ATF3	chr4:7325347-7326029	A549	lung:	n/a	n/a
3	BCL3	chr4:7309477-7309799	GM12878	blood:	n/a	n/a
4	BCL3	chr4:7309436-7309751	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:7297759-7297998	K562	blood:	n/a	chr4:7297811-7297827
6	BHLHE40	chr4:7332888-7333034	K562	blood:	n/a	chr4:7332974-7332983 chr4:7332968-7332989 chr4:7332975-7332984 chr4:7332974-7332983 chr4:7332972-7332985
7	BHLHE40	chr4:7326359-7326668	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:7297755-7297955	GM12878	blood:	n/a	chr4:7297811-7297827
9	BRCA1	chr4:7297940-7298009	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr4:7297835-7297868	GM12878	blood:	n/a	n/a
11	CEBPB	chr4:7314977-7315349	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
12	CEBPB	chr4:7314983-7315346	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
13	CEBPB	chr4:7314937-7315345	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
14	CEBPB	chr4:7315008-7315270	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
15	CEBPB	chr4:7314956-7315381	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
16	CEBPB	chr4:7314975-7315351	IMR90	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
17	CEBPB	chr4:7324654-7324913	IMR90	lung:	n/a	chr4:7324854-7324865
18	CEBPB	chr4:7314905-7315396	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
19	CEBPB	chr4:7314975-7315352	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
20	CEBPB	chr4:7314946-7315363	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
21	CEBPB	chr4:7314977-7315363	H1-hESC	embryonic stem cell:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
22	CEBPB	chr4:7324731-7324857	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:7315082-7315202	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
24	CEBPB	chr4:7314974-7315334	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
25	CEBPB	chr4:7315029-7315275	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
26	CEBPB	chr4:7315017-7315331	Hela-S3	cervix:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
27	CTCF	chr4:7325780-7325930	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:7297661-7298039	K562	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
29	CTCF	chr4:7297759-7297919	A549	lung:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
30	CTCF	chr4:7297638-7298037	H1-hESC	embryonic stem cell:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
31	CTCF	chr4:7297780-7297930	HPF	lung:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
32	CTCF	chr4:7297820-7297970	GM12869	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
33	CTCF	chr4:7325710-7325910	LNCaP	prostate:	n/a	n/a
34	CTCF	chr4:7297780-7297930	HMF	breast:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
35	CTCF	chr4:7325780-7325930	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:7325743-7325913	K562	blood:	n/a	n/a
37	CTCF	chr4:7297820-7297970	GM12866	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
38	CTCF	chr4:7297760-7297910	GM06990	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
39	CTCF	chr4:7297760-7297910	GM12871	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
40	CTCF	chr4:7297800-7297950	AG09319	gingival:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
41	CTCF	chr4:7331660-7331810	GM12871	blood:	n/a	n/a
42	CTCF	chr4:7297880-7298030	HVMF	connective:	n/a	n/a
43	CTCF	chr4:7297880-7298030	HCM	heart:	n/a	n/a
44	CTCF	chr4:7309020-7309170	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:7325796-7325827	IMR90	lung:	n/a	n/a
46	CTCF	chr4:7297800-7297950	GM12873	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
47	CTCF	chr4:7297737-7297993	GM12878	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
48	CTCF	chr4:7297780-7297930	GM12874	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
49	CTCF	chr4:7297780-7297930	AG09319	gingival:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
50	CTCF	chr4:7309100-7309250	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7300999-7301049	HCM	heart:	n/a
2	chr4:7300999-7301049	HCM	heart:	n/a
3	chr4:7301594-7301644	BJ	skin:	n/a
4	chr4:7301529-7301579	Jurkat	blood:	n/a
5	chr4:7301491-7301541	AG04449	skin:	fetal
6	chr4:7330616-7330666	AG04449	skin:	fetal
7	chr4:7301594-7301644	PFSK-1	brain:	n/a
8	chr4:7304739-7304789	GM19239	blood:	n/a
9	chr4:7301529-7301579	AoSMC	blood vessel:	n/a
10	chr4:7301854-7301904	BJ	skin:	n/a
11	chr4:7330616-7330666	NT2-D1	testis:	n/a
12	chr4:7304777-7304827	HRE	kidney:	n/a
13	chr4:7300999-7301049	HCPEpiC	choroid plexus:	n/a
14	chr4:7301491-7301541	IMR90	lung:	fetal
15	chr4:7300999-7301049	HEK293	kidney:	embryo
16	chr4:7300999-7301049	AG04450	lung:	fetal
17	chr4:7300999-7301049	PFSK-1	brain:	n/a
18	chr4:7300999-7301049	HepG2	liver:	n/a
19	chr4:7304777-7304827	HCPEpiC	choroid plexus:	n/a
20	chr4:7301594-7301644	HAEpiC	amniotic membrane:	n/a
21	chr4:7300999-7301049	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:7301491-7301541	HEEpiC	esophagus:	n/a
23	chr4:7301854-7301904	K562	blood:	n/a
24	chr4:7326576-7326626	ovcar-3	ovarian:	n/a
25	chr4:7301529-7301579	HMEC	breast:	n/a
26	chr4:7301854-7301904	CMK	blood:	n/a
27	chr4:7330616-7330666	CMK	blood:	n/a
28	chr4:7301594-7301644	LNCaP	prostate:	n/a
29	chr4:7301823-7301873	HCT-116	colon:	n/a
30	chr4:7304739-7304789	PrEC	prostate:	n/a
31	chr4:7301823-7301873	BE2_C	brain:	n/a
32	chr4:7326576-7326626	NHBE	bronchial:	n/a
33	chr4:7304739-7304789	Caco-2	colon:	n/a
34	chr4:7301594-7301644	SK-N-SH	brain:	n/a
35	chr4:7301823-7301873	AG09309	skin:	n/a
36	chr4:7301823-7301873	A549	lung:	n/a
37	chr4:7326576-7326626	HCM	heart:	n/a
38	chr4:7301854-7301904	HMEC	breast:	n/a
39	chr4:7326576-7326626	GM19239	blood:	n/a
40	chr4:7300999-7301049	GM12878	blood:	n/a
41	chr4:7301594-7301644	Caco-2	colon:	n/a
42	chr4:7301529-7301579	SK-N-SH	brain:	n/a
43	chr4:7301491-7301541	HRCEpiC	kidney:	n/a
44	chr4:7301854-7301904	MCF10A-Er-Src	breast:	n/a
45	chr4:7301594-7301644	ProgFib	skin:	n/a
46	chr4:7326576-7326626	ProgFib	skin:	n/a
47	chr4:7301176-7301226	HRPEpiC	eye:	n/a
48	chr4:7330616-7330666	IMR90	lung:	fetal
49	chr4:7326576-7326626	GM12878	blood:	n/a
50	chr4:7304739-7304789	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
2	chr4:7331028..7333099-chr4:7336513..7338486,2	K562	blood:
3	chr4:7195636..7196730-chr4:7297372..7298445,9	MCF-7	breast:
4	chr4:7200738..7202710-chr4:7296032..7298626,2	MCF-7	breast:
5	chr4:7320638..7322307-chr4:7344162..7346358,2	K562	blood:
6	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
7	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
8	chr4:7193728..7194793-chr4:7297053..7298951,15	MCF-7	breast:
9	chr4:7193764..7194622-chr4:7297791..7298316,3	K562	blood:
10	chr4:7153324..7154166-chr4:7297397..7298037,2	MCF-7	breast:
11	chr4:7207636..7209824-chr4:7302272..7304285,2	MCF-7	breast:
12	chr4:7192934..7196110-chr4:7296657..7299976,3	MCF-7	breast:
13	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
14	chr4:7195671..7196829-chr4:7297061..7298292,4	MCF-7	breast:
15	chr4:7193590..7194707-chr4:7297338..7298352,5	MCF-7	breast:
16	chr4:7196173..7199298-chr4:7297617..7300967,3	MCF-7	breast:
17	chr4:7288760..7290651-chr4:7292846..7295423,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4798-3p	chr4:7312223-7312244	MIMAT0019975
hsa-miR-4798-5p	chr4:7312186-7312207	MIMAT0019974

Variant related genes	Relation type
MIR4798	TF binding region
MIR4798	CpG island
ENSG00000184985	chromatin interactions

Extended variants
information (count: 2024 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2024 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7656453	chr4:7295154-7295155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146937871	chr4:7295198-7295199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545228067	chr4:7295209-7295210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560301547	chr4:7295213-7295214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138200008	chr4:7295305-7295306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527993823	chr4:7295408-7295409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547605052	chr4:7295425-7295426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549238480	chr4:7295432-7295433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370021119	chr4:7295434-7295435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115545491	chr4:7295439-7295440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529927207	chr4:7295440-7295441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550301975	chr4:7295447-7295448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568960335	chr4:7295468-7295469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143771156	chr4:7295561-7295562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376613596	chr4:7295588-7295589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577415592	chr4:7295616-7295617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534081688	chr4:7295617-7295618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555593499	chr4:7295622-7295623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548439110	chr4:7295623-7295624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573842361	chr4:7295637-7295638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538286773	chr4:7295638-7295639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567570150	chr4:7295714-7295715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556264385	chr4:7295731-7295732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577752068	chr4:7295739-7295740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150551160	chr4:7295769-7295770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79241102	chr4:7295772-7295773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112616411	chr4:7295783-7295784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60147274	chr4:7295792-7295793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181570365	chr4:7295793-7295794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561671125	chr4:7295821-7295822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531888927	chr4:7295852-7295853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149581028	chr4:7295878-7295879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144294506	chr4:7295879-7295880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185674929	chr4:7295891-7295892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79781879	chr4:7295895-7295896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192507206	chr4:7295898-7295899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527521939	chr4:7295929-7295930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10937800	chr4:7295943-7295944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183836500	chr4:7295944-7295945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572727057	chr4:7295949-7295950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140095507	chr4:7295993-7295994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542973504	chr4:7296030-7296031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78673260	chr4:7296065-7296066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571279998	chr4:7296075-7296076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538752145	chr4:7296106-7296107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553810425	chr4:7296126-7296127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79178630	chr4:7296134-7296135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188013727	chr4:7296143-7296144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554847251	chr4:7296146-7296147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111355840	chr4:7296148-7296149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7283400-7297000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:7289200-7296800	Weak transcription	Fetal Brain Male	brain
3	chr4:7290400-7296400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:7291600-7297000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:7291800-7297200	Weak transcription	Liver	Liver
6	chr4:7293600-7300200	Weak transcription	Fetal Lung	lung
7	chr4:7293800-7296400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:7293800-7297000	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:7293800-7297000	Weak transcription	Right Atrium	heart
10	chr4:7293800-7297000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr4:7293800-7297200	Weak transcription	Brain Angular Gyrus	brain
12	chr4:7293800-7297200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:7293800-7304400	Weak transcription	Gastric	stomach
14	chr4:7294000-7295200	Weak transcription	Brain Anterior Caudate	brain
15	chr4:7294000-7297000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:7294000-7297000	Weak transcription	Left Ventricle	heart
17	chr4:7294000-7297000	Weak transcription	Ovary	ovary
18	chr4:7294000-7297200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr4:7294000-7297200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:7294200-7295800	Weak transcription	Brain Substantia Nigra	brain
21	chr4:7294200-7296800	Weak transcription	Right Ventricle	heart
22	chr4:7294200-7297000	Weak transcription	Brain Germinal Matrix	brain
23	chr4:7294200-7297200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr4:7294400-7295400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:7294800-7295400	Weak transcription	Brain Hippocampus Middle	brain
26	chr4:7295200-7295600	Enhancers	Brain Anterior Caudate	brain
27	chr4:7295400-7295600	Enhancers	Brain Hippocampus Middle	brain
28	chr4:7295400-7297000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:7295600-7296000	Enhancers	Fetal Brain Female	brain
30	chr4:7295600-7297000	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:7295600-7297200	Weak transcription	Brain Anterior Caudate	brain
32	chr4:7295800-7296200	Enhancers	Brain Substantia Nigra	brain
33	chr4:7296200-7296400	Bivalent Enhancer	Fetal Stomach	stomach
34	chr4:7296200-7297200	Weak transcription	Brain Substantia Nigra	brain
35	chr4:7296400-7296800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:7296400-7297000	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr4:7296400-7297000	Flanking Active TSS	HSMM	muscle
38	chr4:7296800-7297000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:7296800-7297400	Enhancers	Fetal Brain Male	brain
40	chr4:7296800-7297800	Enhancers	Fetal Stomach	stomach
41	chr4:7296800-7298000	Enhancers	Right Ventricle	heart
42	chr4:7296800-7301800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:7297000-7297200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:7297000-7297200	Enhancers	Brain Germinal Matrix	brain
45	chr4:7297000-7297200	Active TSS	Brain Hippocampus Middle	brain
46	chr4:7297000-7297200	Enhancers	Colonic Mucosa	Colon
47	chr4:7297000-7297200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr4:7297000-7297400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:7297000-7297400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr4:7297000-7297400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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