Variant report

Variant	esv3398378
Chromosome Location	chr3:69240573-69271936
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	chr3:69262774-69262889	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:69248519-69248954	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:69261654-69261909	K562	blood:	n/a	n/a
4	ARID3A	chr3:69249635-69250318	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:69261579-69262229	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:69253497-69253930	HepG2	liver:	n/a	n/a
7	ATF1	chr3:69261611-69261887	K562	blood:	n/a	n/a
8	ATF1	chr3:69249683-69250230	K562	blood:	n/a	n/a
9	ATF2	chr3:69255483-69255825	GM12878	blood:	n/a	n/a
10	ATF2	chr3:69253369-69253827	GM12878	blood:	n/a	n/a
11	ATF2	chr3:69255408-69255902	GM12878	blood:	n/a	n/a
12	ATF2	chr3:69253344-69253849	GM12878	blood:	n/a	n/a
13	BATF	chr3:69261561-69261866	GM12878	blood:	n/a	chr3:69261768-69261779
14	BATF	chr3:69256238-69256448	GM12878	blood:	n/a	n/a
15	BATF	chr3:69268541-69268729	GM12878	blood:	n/a	n/a
16	BATF	chr3:69261596-69261897	GM12878	blood:	n/a	chr3:69261768-69261779
17	BATF	chr3:69256236-69256458	GM12878	blood:	n/a	n/a
18	BATF	chr3:69253405-69253989	GM12878	blood:	n/a	n/a
19	BATF	chr3:69253444-69253731	GM12878	blood:	n/a	n/a
20	BATF	chr3:69255492-69255819	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:69255489-69255831	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:69253448-69253667	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:69253399-69253773	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:69248612-69248839	GM12878	blood:	n/a	n/a
25	BCL3	chr3:69253380-69253684	GM12878	blood:	n/a	n/a
26	BCL3	chr3:69255475-69255862	GM12878	blood:	n/a	n/a
27	BCL3	chr3:69261579-69262367	A549	lung:	n/a	chr3:69261617-69261626
28	BRCA1	chr3:69261618-69262173	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:69249476-69250501	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr3:69250078-69250190	K562	blood:	n/a	n/a
31	CEBPB	chr3:69247128-69247329	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:69242987-69243172	IMR90	lung:	n/a	chr3:69243083-69243094 chr3:69243084-69243093
33	CEBPB	chr3:69267231-69267613	K562	blood:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
34	CEBPB	chr3:69267338-69267494	K562	blood:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267419-69267428 chr3:69267417-69267428
35	CEBPB	chr3:69248851-69248978	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:69267247-69267607	H1-hESC	embryonic stem cell:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
37	CEBPB	chr3:69255405-69255977	GM12878	blood:	n/a	chr3:69255598-69255611 chr3:69255597-69255614
38	CEBPB	chr3:69267234-69267585	Hela-S3	cervix:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
39	CEBPB	chr3:69261638-69261946	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:69267310-69267522	K562	blood:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
41	CEBPB	chr3:69261549-69262343	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:69267248-69267603	IMR90	lung:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
43	CEBPB	chr3:69261597-69262217	A549	lung:	n/a	n/a
44	CEBPB	chr3:69249476-69250305	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr3:69247109-69247372	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:69267157-69267703	A549	lung:	n/a	chr3:69267419-69267428 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267418-69267429 chr3:69267417-69267430 chr3:69267417-69267430 chr3:69267419-69267428 chr3:69267334-69267345 chr3:69267419-69267428 chr3:69267417-69267428
47	CEBPB	chr3:69261559-69262325	MCF-7	breast:	n/a	n/a
48	CEBPB	chr3:69249544-69250251	MCF-7	breast:	n/a	n/a
49	CEBPB	chr3:69261601-69261914	K562	blood:	n/a	n/a
50	CEBPB	chr3:69261531-69262372	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69249276-69249326	HRE	kidney:	n/a
2	chr3:69249276-69249326	HNPCEpiC	eye:	n/a
3	chr3:69249276-69249326	A549	lung:	n/a
4	chr3:69249276-69249326	NT2-D1	testis:	n/a
5	chr3:69249276-69249326	HCT-116	colon:	n/a
6	chr3:69249276-69249326	HRCEpiC	kidney:	n/a
7	chr3:69249276-69249326	SAEC	small airway:	n/a
8	chr3:69249276-69249326	AoSMC	blood vessel:	n/a
9	chr3:69249276-69249326	NB4	blood:	n/a
10	chr3:69249276-69249326	SKMC	muscle:	n/a
11	chr3:69249276-69249326	NHBE	bronchial:	n/a
12	chr3:69249276-69249326	BE2_C	brain:	n/a
13	chr3:69249276-69249326	GM12892	blood:	n/a
14	chr3:69249276-69249326	HMEC	breast:	n/a
15	chr3:69249276-69249326	HepG2	liver:	n/a
16	chr3:69249276-69249326	U87	brain:	n/a
17	chr3:69249276-69249326	AG10803	skin:	n/a
18	chr3:69249276-69249326	BJ	skin:	n/a
19	chr3:69249276-69249326	ProgFib	skin:	n/a
20	chr3:69249276-69249326	HAEpiC	amniotic membrane:	n/a
21	chr3:69249276-69249326	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:69249276-69249326	MCF-7	breast:	n/a
23	chr3:69249276-69249326	HCPEpiC	choroid plexus:	n/a
24	chr3:69249276-69249326	SK-N-SH_RA	brain:	n/a
25	chr3:69249276-69249326	HCF	heart:	n/a
26	chr3:69249276-69249326	AG09309	skin:	n/a
27	chr3:69249276-69249326	AG04449	skin:	fetal
28	chr3:69249276-69249326	SK-N-SH	brain:	n/a
29	chr3:69249276-69249326	ovcar-3	ovarian:	n/a
30	chr3:69249276-69249326	NHDF-neo	bronchial:	n/a
31	chr3:69249276-69249326	CMK	blood:	n/a
32	chr3:69249276-69249326	HEK293	kidney:	embryo
33	chr3:69249276-69249326	GM19239	blood:	n/a
34	chr3:69249276-69249326	Hela-S3	cervix:	n/a
35	chr3:69249276-69249326	HRPEpiC	eye:	n/a
36	chr3:69249276-69249326	H1-hESC	embryonic stem cell:	embryo
37	chr3:69249276-69249326	Jurkat	blood:	n/a
38	chr3:69249276-69249326	PFSK-1	brain:	n/a
39	chr3:69249276-69249326	PrEC	prostate:	n/a
40	chr3:69249276-69249326	Caco-2	colon:	n/a
41	chr3:69249276-69249326	MCF10A-Er-Src	breast:	n/a
42	chr3:69249276-69249326	GM06990	blood:	n/a
43	chr3:69249276-69249326	SK-N-MC	brain:	n/a
44	chr3:69249276-69249326	NH-A	brain:	n/a
45	chr3:69249276-69249326	K562	blood:	n/a
46	chr3:69249276-69249326	HL-60	blood:	n/a
47	chr3:69249276-69249326	GM12878	blood:	n/a
48	chr3:69249276-69249326	T-47D	breast:	n/a
49	chr3:69249276-69249326	HUVEC	blood vessel:	n/a
50	chr3:69249276-69249326	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:69243953..69247149-chr3:69247614..69251113,3	MCF-7	breast:
2	chr3:69249207..69251218-chr3:69257048..69259660,2	MCF-7	breast:
3	chr3:69242995..69248050-chr3:69248288..69251594,5	MCF-7	breast:
4	chr3:69271768..69274528-chr3:69280335..69282349,2	MCF-7	breast:
5	chr3:69250039..69253834-chr3:69260660..69262607,3	MCF-7	breast:
6	chr3:69237366..69240116-chr3:69241157..69243942,2	MCF-7	breast:
7	chr3:69261818..69263974-chr3:69274999..69277615,2	MCF-7	breast:
8	chr3:69241267..69243514-chr3:69247620..69250040,3	MCF-7	breast:

Variant related genes	Relation type
FRMD4B	TF binding region
FRMD4B	CpG island
ENSG00000114541	chromatin interactions

Extended variants
information (count: 1490 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1490 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139554201	chr3:69240574-69240575	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs386662070	chr3:69240583-69240584	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201240530	chr3:69240594-69240595	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60163276	chr3:69240601-69240602	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73835776	chr3:69240610-69240611	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557253542	chr3:69240652-69240653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181750135	chr3:69240687-69240688	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112943881	chr3:69240708-69240709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113585781	chr3:69240709-69240710	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397975438	chr3:69240710-69240711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115632423	chr3:69240770-69240771	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186937607	chr3:69240776-69240777	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528424706	chr3:69240828-69240829	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75927483	chr3:69240853-69240854	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190089353	chr3:69240875-69240876	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529330514	chr3:69240975-69240976	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571447739	chr3:69240979-69240980	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376823660	chr3:69241027-69241028	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377410562	chr3:69241046-69241047	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181038507	chr3:69241109-69241110	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185507417	chr3:69241120-69241121	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73114364	chr3:69241262-69241263	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567331373	chr3:69241265-69241266	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529926946	chr3:69241313-69241314	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543050840	chr3:69241316-69241317	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs149295580	chr3:69241329-69241330	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566775084	chr3:69241338-69241339	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538596235	chr3:69241362-69241363	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs559486859	chr3:69241371-69241372	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558257187	chr3:69241397-69241398	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115961582	chr3:69241398-69241399	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528812027	chr3:69241431-69241432	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554665092	chr3:69241432-69241433	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146253680	chr3:69241460-69241461	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536454259	chr3:69241497-69241498	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533830406	chr3:69241519-69241520	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4508787	chr3:69241585-69241586	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs111288320	chr3:69241603-69241604	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565110734	chr3:69241616-69241617	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112990063	chr3:69241632-69241633	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs57765607	chr3:69241643-69241644	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs79305552	chr3:69241673-69241674	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142683480	chr3:69241674-69241675	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145929653	chr3:69241678-69241679	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs58110267	chr3:69241699-69241700	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs77741737	chr3:69241721-69241722	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs4498053	chr3:69241723-69241724	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs80097137	chr3:69241726-69241727	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554051628	chr3:69241743-69241744	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552479555	chr3:69241749-69241750	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69218400-69247400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr3:69218400-69247800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:69222800-69245400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr3:69226800-69246800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr3:69228400-69246800	Weak transcription	Primary T cells from cord blood	blood
6	chr3:69228600-69248600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr3:69228800-69241200	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr3:69228800-69245800	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr3:69228800-69246000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr3:69229000-69248400	Weak transcription	Primary B cells from cord blood	blood
11	chr3:69229200-69246000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:69229600-69248200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr3:69230600-69243000	Weak transcription	Fetal Kidney	kidney
14	chr3:69230600-69248600	Weak transcription	Aorta	Aorta
15	chr3:69230600-69248600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr3:69230800-69248600	Weak transcription	Ovary	ovary
17	chr3:69231000-69240800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:69231000-69240800	Weak transcription	Esophagus	oesophagus
19	chr3:69231000-69240800	Weak transcription	Spleen	Spleen
20	chr3:69231000-69243600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:69231200-69246800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr3:69231200-69248600	Weak transcription	Left Ventricle	heart
23	chr3:69231200-69248600	Weak transcription	Small Intestine	intestine
24	chr3:69231400-69246400	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr3:69231400-69246600	Weak transcription	Fetal Brain Male	brain
26	chr3:69231400-69248400	Weak transcription	Rectal Smooth Muscle	rectum
27	chr3:69231400-69249600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:69231600-69248600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:69231800-69249600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:69232000-69247400	Weak transcription	Hela-S3	cervix
31	chr3:69232000-69248800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:69232000-69249400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr3:69232000-69275600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:69232200-69248600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr3:69232400-69246600	Strong transcription	Placenta	Placenta
36	chr3:69232400-69247400	Weak transcription	Stomach Mucosa	stomach
37	chr3:69232400-69248400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:69232400-69248400	Weak transcription	Brain Angular Gyrus	brain
39	chr3:69232600-69242800	Weak transcription	HSMMtube	muscle
40	chr3:69232600-69246000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr3:69232800-69249200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:69233200-69247200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:69233200-69247800	Strong transcription	Fetal Intestine Large	intestine
44	chr3:69233400-69242800	Strong transcription	HUVEC	blood vessel
45	chr3:69233400-69246600	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr3:69233600-69241600	Strong transcription	Adipose Nuclei	Adipose
47	chr3:69233600-69247400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr3:69233600-69247800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr3:69234000-69240600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr3:69234000-69246600	Strong transcription	Rectal Mucosa Donor 29	rectum

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