Variant report

Variant	esv14217
Chromosome Location	chr7:32999213-33053044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:33018936-33019182	K562	blood:	n/a	n/a
2	BATF	chr7:33004344-33004651	GM12878	blood:	n/a	n/a
3	BATF	chr7:33013146-33013310	GM12878	blood:	n/a	n/a
4	BATF	chr7:33013068-33013309	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:33004460-33004702	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:33027956-33028178	HepG2	liver:	n/a	n/a
7	CBX3	chr7:33037995-33038493	K562	blood:	n/a	n/a
8	CEBPB	chr7:33032833-33033019	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:33011231-33011349	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:33016891-33017017	HepG2	liver:	n/a	chr7:33016937-33016948
11	CEBPB	chr7:33032892-33033009	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:33016866-33017097	A549	lung:	n/a	chr7:33016937-33016948
13	CEBPB	chr7:33018898-33019225	IMR90	lung:	n/a	chr7:33019062-33019075
14	CEBPB	chr7:33027942-33028079	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:33012682-33013047	Hela-S3	cervix:	n/a	chr7:33012846-33012857 chr7:33012846-33012857
16	CEBPB	chr7:33012027-33012222	Hela-S3	cervix:	n/a	chr7:33012145-33012156 chr7:33012083-33012096
17	CEBPB	chr7:33045047-33045051	K562	blood:	n/a	n/a
18	CEBPB	chr7:33016815-33017087	Hela-S3	cervix:	n/a	chr7:33016937-33016948
19	CEBPB	chr7:33032827-33033008	K562	blood:	n/a	n/a
20	CEBPB	chr7:33006795-33007049	IMR90	lung:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
21	CEBPB	chr7:33006777-33007058	HepG2	liver:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
22	CEBPB	chr7:33018876-33019216	K562	blood:	n/a	chr7:33019062-33019075
23	CEBPB	chr7:33018925-33019185	A549	lung:	n/a	chr7:33019062-33019075
24	CEBPB	chr7:33044969-33045200	HepG2	liver:	n/a	chr7:33045054-33045065
25	CEBPB	chr7:33006792-33006999	Hela-S3	cervix:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
26	CEBPB	chr7:33006754-33007063	K562	blood:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
27	CEBPB	chr7:33006797-33007009	A549	lung:	n/a	chr7:33006947-33006958 chr7:33006917-33006928
28	CEBPB	chr7:33032788-33033110	K562	blood:	n/a	n/a
29	CEBPB	chr7:33018906-33019175	K562	blood:	n/a	chr7:33019062-33019075
30	CEBPB	chr7:33032846-33033019	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:33018921-33019124	H1-hESC	embryonic stem cell:	n/a	chr7:33019062-33019075
32	CEBPB	chr7:33018853-33019276	Hela-S3	cervix:	n/a	chr7:33019062-33019075
33	CHD2	chr7:33018941-33019169	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr7:33038220-33038370	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr7:33004343-33004626	GM10266	blood:	n/a	n/a
36	CTCF	chr7:33004520-33004670	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr7:33004620-33004770	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr7:33004140-33004430	GM06990	blood:	n/a	n/a
39	CTCF	chr7:33004640-33004790	GM12873	blood:	n/a	n/a
40	CTCF	chr7:33004280-33004430	HMEC	breast:	n/a	n/a
41	CTCF	chr7:33004620-33004770	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:33004280-33004430	AG09309	skin:	n/a	n/a
43	CTCF	chr7:33004342-33004633	GM19240	blood:	n/a	n/a
44	CTCF	chr7:33004620-33004770	RPTEC	kidney:	n/a	n/a
45	CTCF	chr7:33004359-33004628	A549	lung:	n/a	n/a
46	CTCF	chr7:33043885-33043976	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:33027321-33027333	Lung_OC	lung:	n/a	n/a
48	CTCF	chr7:33004314-33004615	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr7:33004363-33004597	GM10248	blood:	n/a	n/a
50	CTCF	chr7:33004600-33004750	BJ	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33001327-33001377	NH-A	brain:	n/a
2	chr7:33001327-33001377	HEK293	kidney:	embryo
3	chr7:33001327-33001377	H1-hESC	embryonic stem cell:	embryo
4	chr7:33046274-33046324	NH-A	brain:	n/a
5	chr7:33046274-33046324	MCF10A-Er-Src	breast:	n/a
6	chr7:33046274-33046324	ovcar-3	ovarian:	n/a
7	chr7:33046274-33046324	HNPCEpiC	eye:	n/a
8	chr7:33001327-33001377	Hela-S3	cervix:	n/a
9	chr7:33046274-33046324	SK-N-SH	brain:	n/a
10	chr7:33046274-33046324	AG09309	skin:	n/a
11	chr7:33001327-33001377	HepG2	liver:	n/a
12	chr7:33001327-33001377	NHBE	bronchial:	n/a
13	chr7:33001327-33001377	Hepatocyte	liver:	n/a
14	chr7:33046274-33046324	K562	blood:	n/a
15	chr7:33046274-33046324	HUVEC	blood vessel:	n/a
16	chr7:33001327-33001377	SK-N-SH_RA	brain:	n/a
17	chr7:33046274-33046324	GM12892	blood:	n/a
18	chr7:33001327-33001377	HCPEpiC	choroid plexus:	n/a
19	chr7:33001327-33001377	SK-N-MC	brain:	n/a
20	chr7:33001327-33001377	HCM	heart:	n/a
21	chr7:33046274-33046324	NHBE	bronchial:	n/a
22	chr7:33001327-33001377	HRCEpiC	kidney:	n/a
23	chr7:33046274-33046324	GM19239	blood:	n/a
24	chr7:33046274-33046324	HEK293	kidney:	embryo
25	chr7:33046274-33046324	AG04450	lung:	fetal
26	chr7:33001327-33001377	HCT-116	colon:	n/a
27	chr7:33001327-33001377	RPTEC	kidney:	n/a
28	chr7:33001327-33001377	HCF	heart:	n/a
29	chr7:33046274-33046324	U87	brain:	n/a
30	chr7:33001327-33001377	Caco-2	colon:	n/a
31	chr7:33001327-33001377	PFSK-1	brain:	n/a
32	chr7:33046274-33046324	AG09319	gingival:	n/a
33	chr7:33001327-33001377	GM19239	blood:	n/a
34	chr7:33001327-33001377	GM12892	blood:	n/a
35	chr7:33046274-33046324	MCF-7	breast:	n/a
36	chr7:33001327-33001377	HEEpiC	esophagus:	n/a
37	chr7:33001327-33001377	HUVEC	blood vessel:	n/a
38	chr7:33001327-33001377	K562	blood:	n/a
39	chr7:33046274-33046324	SK-N-MC	brain:	n/a
40	chr7:33046274-33046324	HRPEpiC	eye:	n/a
41	chr7:33001327-33001377	BE2_C	brain:	n/a
42	chr7:33001327-33001377	HNPCEpiC	eye:	n/a
43	chr7:33001327-33001377	MCF-7	breast:	n/a
44	chr7:33001327-33001377	NHDF-neo	bronchial:	n/a
45	chr7:33046274-33046324	LNCaP	prostate:	n/a
46	chr7:33046274-33046324	HEEpiC	esophagus:	n/a
47	chr7:33046274-33046324	BJ	skin:	n/a
48	chr7:33046274-33046324	AoSMC	blood vessel:	n/a
49	chr7:33046274-33046324	PFSK-1	brain:	n/a
50	chr7:33046274-33046324	Jurkat	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:32996093..32998433-chr7:33003522..33005061,2	MCF-7	breast:
2	chr7:33045709..33047720-chr7:33048336..33051213,2	K562	blood:
3	chr7:33049778..33053350-chr7:33054534..33056757,3	K562	blood:
4	chr7:33045709..33047720-chr7:33048336..33051213,2	K562	blood:
5	chr7:33049567..33051486-chr7:33100802..33103413,2	MCF-7	breast:
6	chr7:32997687..32999563-chr7:33147479..33150290,2	K562	blood:
7	chr7:32981007..32984575-chr7:32996149..32999305,3	K562	blood:
8	chr7:33048890..33051956-chr7:33060323..33062339,3	K562	blood:
9	chr7:33004263..33004782-chr7:33090500..33091470,2	MCF-7	breast:
10	chr7:32996766..32998569-chr7:33027965..33030293,2	K562	blood:
11	chr7:32996678..32998583-chr7:33000534..33003060,3	MCF-7	breast:
12	chr7:32982489..32988008-chr7:32995538..32999914,10	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-388P	TF binding region
FKBP9	TF binding region
RNU6-388P	CpG island
FKBP9	CpG island
ENSG00000205763	chromatin interactions
ENSG00000122643	chromatin interactions
ENSG00000122642	chromatin interactions
ENSG00000164610	chromatin interactions

Extended variants
information (count: 2136 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185126595	chr7:32999224-32999225	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547923741	chr7:32999227-32999228	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375953731	chr7:32999243-32999244	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs566146545	chr7:32999278-32999279	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539642627	chr7:32999292-32999293	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs140372292	chr7:32999314-32999315	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112763857	chr7:32999342-32999343	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569196929	chr7:32999379-32999380	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188372928	chr7:32999380-32999381	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554990519	chr7:32999381-32999382	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201685985	chr7:32999419-32999420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573305082	chr7:32999465-32999466	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540583200	chr7:32999472-32999473	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559036183	chr7:32999473-32999474	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577634388	chr7:32999480-32999481	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs10266139	chr7:32999498-32999499	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs78811678	chr7:32999507-32999508	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566960377	chr7:32999544-32999545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs115274482	chr7:32999549-32999550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs13311608	chr7:32999601-32999602	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs369609734	chr7:32999646-32999647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562329600	chr7:32999665-32999666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34736849	chr7:32999719-32999720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs70989910	chr7:32999721-32999722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs398004304	chr7:32999741-32999742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs13311772	chr7:32999810-32999811	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs181363835	chr7:32999819-32999820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10251280	chr7:32999884-32999885	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs566207700	chr7:32999934-32999935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539535607	chr7:32999952-32999953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551594067	chr7:32999958-32999959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569747473	chr7:33000006-33000007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140452990	chr7:33000051-33000052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555251367	chr7:33000082-33000083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573563284	chr7:33000127-33000128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556414433	chr7:33000128-33000129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111977801	chr7:33000136-33000137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71532544	chr7:33000141-33000142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369591991	chr7:33000145-33000146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577700034	chr7:33000154-33000155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544765730	chr7:33000192-33000193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563687211	chr7:33000252-33000253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111991731	chr7:33000267-33000268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576572734	chr7:33000323-33000324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543999036	chr7:33000329-33000330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562391758	chr7:33000347-33000348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529591112	chr7:33000408-33000409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186515286	chr7:33000419-33000420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143937133	chr7:33000442-33000443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533515697	chr7:33000471-33000472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:32998200-33038600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr7:32998400-33000200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:32998400-33001800	Weak transcription	Fetal Brain Male	brain
4	chr7:32998400-33003000	Weak transcription	Fetal Kidney	kidney
5	chr7:32998400-33003400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr7:32998400-33003400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:32998400-33003600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr7:32998400-33011200	Weak transcription	Gastric	stomach
9	chr7:32998600-32999400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:32998600-32999400	Enhancers	Adipose Nuclei	Adipose
11	chr7:32998600-32999400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr7:32998600-32999400	Enhancers	NHDF-Ad	bronchial
13	chr7:32998600-32999400	Enhancers	NHEK	skin
14	chr7:32998600-32999600	Enhancers	HepG2	liver
15	chr7:32998600-33000400	Weak transcription	Liver	Liver
16	chr7:32998600-33002600	Weak transcription	Fetal Intestine Small	intestine
17	chr7:32998600-33003000	Weak transcription	Fetal Lung	lung
18	chr7:32998600-33003200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:32998600-33003200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:32998600-33003200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:32998600-33003200	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:32998600-33003200	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:32998600-33003200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr7:32998600-33003400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:32998600-33003400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:32998600-33003400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:32998600-33003400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:32998600-33003400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr7:32998600-33003400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:32998600-33003400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:32998600-33003400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:32998600-33003400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr7:32998600-33003400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr7:32998600-33003400	Weak transcription	Fetal Intestine Large	intestine
35	chr7:32998600-33003400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr7:32998600-33003400	Weak transcription	Placenta	Placenta
37	chr7:32998600-33003400	Weak transcription	Fetal Stomach	stomach
38	chr7:32998600-33003400	Weak transcription	Left Ventricle	heart
39	chr7:32998600-33003400	Weak transcription	Ovary	ovary
40	chr7:32998600-33003400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr7:32998600-33003400	Weak transcription	K562	blood
42	chr7:32998600-33003600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:32998600-33003600	Weak transcription	Brain Germinal Matrix	brain
44	chr7:32998600-33003600	Weak transcription	Esophagus	oesophagus
45	chr7:32998600-33003600	Weak transcription	HMEC	breast
46	chr7:32998600-33003600	Weak transcription	NHLF	lung
47	chr7:32998600-33003800	Weak transcription	Stomach Mucosa	stomach
48	chr7:32998600-33004000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr7:32998600-33011200	Weak transcription	A549	lung
50	chr7:32998600-33014200	Weak transcription	HSMMtube	muscle

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