Variant report

Variant	nsv4808
Chromosome Location	chr5:41203254-41251985
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	chr5:41213191-41214684	HepG2	liver:	n/a	n/a
2	ATF3	chr5:41246392-41246946	HCT-116	colon:	n/a	n/a
3	BRCA1	chr5:41240821-41240843	HepG2	liver:	n/a	n/a
4	CBX3	chr5:41246411-41246897	HCT-116	colon:	n/a	n/a
5	CEBPB	chr5:41220737-41221029	HepG2	liver:	n/a	chr5:41220862-41220873
6	CEBPB	chr5:41219455-41219720	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:41220709-41221005	IMR90	lung:	n/a	chr5:41220862-41220873
8	CEBPB	chr5:41213504-41213865	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:41234483-41234619	A549	lung:	n/a	chr5:41234527-41234538 chr5:41234488-41234501 chr5:41234527-41234538
10	CEBPB	chr5:41246463-41246824	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:41224094-41224354	IMR90	lung:	n/a	chr5:41224214-41224225
12	CEBPB	chr5:41223426-41223675	HepG2	liver:	n/a	chr5:41223491-41223500
13	CEBPB	chr5:41246338-41246952	HCT-116	colon:	n/a	n/a
14	CEBPB	chr5:41224080-41224337	HepG2	liver:	n/a	chr5:41224214-41224225
15	CTCF	chr5:41248821-41248831	GM10266	blood:	n/a	n/a
16	CTCF	chr5:41218780-41218930	AG09319	gingival:	n/a	n/a
17	CTCF	chr5:41241180-41241330	GM12873	blood:	n/a	n/a
18	CTCF	chr5:41213544-41213699	Medullo	brain:	n/a	n/a
19	CTCF	chr5:41248845-41248858	GM10266	blood:	n/a	n/a
20	CTCF	chr5:41241140-41241290	GM12873	blood:	n/a	n/a
21	CTCF	chr5:41222228-41222253	LNCaP	prostate:	n/a	n/a
22	E2F4	chr5:41221001-41221123	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr5:41245853-41246044	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr5:41217316-41217495	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr5:41246569-41246834	MCF10A-Er-Src	breast:	n/a	n/a
26	EP300	chr5:41246360-41246941	SK-N-SH	brain:	n/a	chr5:41246673-41246682
27	EP300	chr5:41230101-41231053	SK-N-SH	brain:	n/a	n/a
28	EP300	chr5:41230377-41230739	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr5:41233291-41233335	K562	blood:	n/a	n/a
30	EP300	chr5:41246517-41246799	SK-N-SH_RA	brain:	n/a	chr5:41246673-41246682
31	EP300	chr5:41213567-41213810	HepG2	liver:	n/a	n/a
32	EP300	chr5:41230333-41230756	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr5:41213269-41213778	HepG2	liver:	n/a	n/a
34	EP300	chr5:41213543-41213797	HepG2	liver:	n/a	n/a
35	FOS	chr5:41246326-41246903	MCF10A-Er-Src	breast:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
36	FOS	chr5:41246407-41246949	MCF10A-Er-Src	breast:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
37	FOS	chr5:41246369-41247067	MCF10A-Er-Src	breast:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
38	FOS	chr5:41246441-41246862	MCF10A-Er-Src	breast:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
39	FOSL1	chr5:41246273-41247001	HCT-116	colon:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
40	FOSL1	chr5:41246360-41246940	HCT-116	colon:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
41	FOSL2	chr5:41246432-41246754	MCF-7	breast:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
42	FOSL2	chr5:41246304-41246915	SK-N-SH	brain:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
43	FOSL2	chr5:41246433-41246903	A549	lung:	n/a	chr5:41246672-41246682 chr5:41246672-41246681 chr5:41246671-41246683 chr5:41246674-41246685 chr5:41246672-41246682 chr5:41246672-41246682 chr5:41246672-41246682
44	FOXA1	chr5:41213468-41213828	HepG2	liver:	n/a	n/a
45	FOXA2	chr5:41213563-41213788	HepG2	liver:	n/a	n/a
46	GATA2	chr5:41230351-41230797	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr5:41246321-41246960	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr5:41230418-41230766	T-47D	breast:	n/a	n/a
49	GATA3	chr5:41216340-41216347	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr5:41246307-41246930	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:41205519-41205569	GM12892	blood:	n/a
2	chr5:41219519-41219569	ovcar-3	ovarian:	n/a
3	chr5:41219519-41219569	HRPEpiC	eye:	n/a
4	chr5:41219519-41219569	T-47D	breast:	n/a
5	chr5:41213172-41213222	ProgFib	skin:	n/a
6	chr5:41213172-41213222	T-47D	breast:	n/a
7	chr5:41213172-41213222	HAEpiC	amniotic membrane:	n/a
8	chr5:41213172-41213222	GM12892	blood:	n/a
9	chr5:41205519-41205569	T-47D	breast:	n/a
10	chr5:41213172-41213222	GM12878	blood:	n/a
11	chr5:41219519-41219569	U87	brain:	n/a
12	chr5:41213172-41213222	HCT-116	colon:	n/a
13	chr5:41219519-41219569	HL-60	blood:	n/a
14	chr5:41213172-41213222	AG09309	skin:	n/a
15	chr5:41219519-41219569	LNCaP	prostate:	n/a
16	chr5:41219519-41219569	NHBE	bronchial:	n/a
17	chr5:41213172-41213222	Hepatocyte	liver:	n/a
18	chr5:41205519-41205569	SKMC	muscle:	n/a
19	chr5:41213172-41213222	HCPEpiC	choroid plexus:	n/a
20	chr5:41213172-41213222	HUVEC	blood vessel:	n/a
21	chr5:41213172-41213222	MCF10A-Er-Src	breast:	n/a
22	chr5:41205519-41205569	HCF	heart:	n/a
23	chr5:41205519-41205569	GM12878	blood:	n/a
24	chr5:41219519-41219569	IMR90	lung:	fetal
25	chr5:41205519-41205569	K562	blood:	n/a
26	chr5:41213172-41213222	U87	brain:	n/a
27	chr5:41213172-41213222	NHBE	bronchial:	n/a
28	chr5:41219519-41219569	NH-A	brain:	n/a
29	chr5:41213172-41213222	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:41219519-41219569	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:41219519-41219569	HAEpiC	amniotic membrane:	n/a
32	chr5:41205519-41205569	HL-60	blood:	n/a
33	chr5:41213172-41213222	AG04450	lung:	fetal
34	chr5:41205519-41205569	GM19239	blood:	n/a
35	chr5:41219519-41219569	Hela-S3	cervix:	n/a
36	chr5:41213172-41213222	AG04449	skin:	fetal
37	chr5:41205519-41205569	NT2-D1	testis:	n/a
38	chr5:41219519-41219569	HCF	heart:	n/a
39	chr5:41213172-41213222	PFSK-1	brain:	n/a
40	chr5:41213172-41213222	HNPCEpiC	eye:	n/a
41	chr5:41219519-41219569	A549	lung:	n/a
42	chr5:41213172-41213222	BE2_C	brain:	n/a
43	chr5:41213172-41213222	GM19239	blood:	n/a
44	chr5:41219519-41219569	SK-N-SH_RA	brain:	n/a
45	chr5:41205519-41205569	PrEC	prostate:	n/a
46	chr5:41213172-41213222	LNCaP	prostate:	n/a
47	chr5:41213172-41213222	Jurkat	blood:	n/a
48	chr5:41213172-41213222	SK-N-SH_RA	brain:	n/a
49	chr5:41219519-41219569	HIPEpiC	eye:	n/a
50	chr5:41213172-41213222	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:41245805..41247360-chr5:41249520..41252230,2	MCF-7	breast:
2	chr5:41243368..41245304-chr5:41252491..41255369,2	K562	blood:
3	chr5:41246537..41249382-chr5:41272514..41274880,2	K562	blood:
4	chr5:41245805..41247360-chr5:41249520..41252230,2	MCF-7	breast:

Variant related genes	Relation type
C6	TF binding region
C6	CpG island

Extended variants
information (count: 1468 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1468 , 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	rs544418156	chr5:41203268-41203269	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369644769	chr5:41203291-41203292	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372263718	chr5:41203303-41203304	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148402406	chr5:41203305-41203306	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377251152	chr5:41203312-41203313	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146127832	chr5:41203322-41203323	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150931891	chr5:41203323-41203324	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201811507	chr5:41203334-41203335	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2305060	chr5:41203344-41203345	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs373196043	chr5:41203369-41203370	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376126899	chr5:41203370-41203371	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369549926	chr5:41203379-41203380	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138981054	chr5:41203402-41203403	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs180816148	chr5:41203404-41203405	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552807465	chr5:41203486-41203487	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142226265	chr5:41203506-41203507	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375203571	chr5:41203507-41203508	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186049995	chr5:41203533-41203534	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75946237	chr5:41203547-41203548	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535096696	chr5:41203551-41203552	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191300504	chr5:41203554-41203555	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181321694	chr5:41203588-41203589	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185900229	chr5:41203693-41203694	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2120824	chr5:41203711-41203712	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576202091	chr5:41203762-41203763	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139458770	chr5:41203834-41203835	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556417877	chr5:41203844-41203845	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574955133	chr5:41203929-41203930	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542268490	chr5:41203949-41203950	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6863479	chr5:41203957-41203958	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376049371	chr5:41203972-41203973	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183173502	chr5:41203983-41203984	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10155551	chr5:41204004-41204005	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs564799908	chr5:41204007-41204008	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531843347	chr5:41204080-41204081	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113235303	chr5:41204096-41204097	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74342457	chr5:41204097-41204098	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144469403	chr5:41204146-41204147	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546995045	chr5:41204172-41204173	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139577988	chr5:41204173-41204174	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532760407	chr5:41204183-41204184	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551416890	chr5:41204191-41204192	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186382335	chr5:41204300-41204301	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111777334	chr5:41204301-41204302	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1444903	chr5:41204303-41204304	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543576477	chr5:41204328-41204329	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147610244	chr5:41204332-41204333	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111307715	chr5:41204343-41204344	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554299599	chr5:41204363-41204364	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563349832	chr5:41204452-41204453	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Type 2 diabetes	21526130	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41195600-41205400	Weak transcription	Pancreas	Pancrea
2	chr5:41200800-41204400	Genic enhancers	Liver	Liver
3	chr5:41201600-41204000	Weak transcription	Fetal Intestine Large	intestine
4	chr5:41203200-41204200	Enhancers	Fetal Intestine Small	intestine
5	chr5:41204000-41204200	Enhancers	Fetal Intestine Large	intestine
6	chr5:41204200-41204800	Weak transcription	Fetal Intestine Large	intestine
7	chr5:41204200-41204800	Weak transcription	Fetal Intestine Small	intestine
8	chr5:41204400-41205400	Strong transcription	Liver	Liver
9	chr5:41204800-41206000	ZNF genes & repeats	Fetal Intestine Large	intestine
10	chr5:41204800-41206200	ZNF genes & repeats	Fetal Intestine Small	intestine
11	chr5:41205400-41206000	ZNF genes & repeats	Pancreas	Pancrea
12	chr5:41205400-41206200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:41205400-41206200	ZNF genes & repeats	Liver	Liver
14	chr5:41206000-41207200	Weak transcription	Pancreas	Pancrea
15	chr5:41206000-41211600	Weak transcription	Fetal Intestine Large	intestine
16	chr5:41206200-41207200	Weak transcription	Liver	Liver
17	chr5:41206200-41211600	Weak transcription	Fetal Intestine Small	intestine
18	chr5:41207200-41207800	Enhancers	Liver	Liver
19	chr5:41207800-41208000	Flanking Active TSS	Liver	Liver
20	chr5:41208000-41208400	Active TSS	Liver	Liver
21	chr5:41208400-41209800	Weak transcription	Liver	Liver
22	chr5:41209800-41213800	Active TSS	Liver	Liver
23	chr5:41211400-41211800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:41211400-41213800	Active TSS	Right Atrium	heart
25	chr5:41211600-41212000	Enhancers	Fetal Intestine Large	intestine
26	chr5:41211600-41213600	Active TSS	Fetal Intestine Small	intestine
27	chr5:41211600-41213600	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr5:41211800-41212800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:41212000-41213600	Active TSS	Fetal Intestine Large	intestine
30	chr5:41212400-41213200	Active TSS	Pancreas	Pancrea
31	chr5:41212800-41213600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:41212800-41213600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:41212800-41213600	Active TSS	Right Ventricle	heart
34	chr5:41212800-41215200	Enhancers	HepG2	liver
35	chr5:41213000-41213600	Enhancers	Stomach Mucosa	stomach
36	chr5:41213000-41213800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr5:41213600-41213800	Weak transcription	Fetal Intestine Large	intestine
38	chr5:41213600-41214000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:41213600-41214000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr5:41213600-41214200	Weak transcription	Fetal Intestine Small	intestine
41	chr5:41213800-41214000	Flanking Active TSS	Liver	Liver
42	chr5:41213800-41215400	Enhancers	Fetal Intestine Large	intestine
43	chr5:41214000-41214200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr5:41214000-41214400	Enhancers	Liver	Liver
45	chr5:41214000-41218600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:41214200-41215000	Enhancers	Fetal Intestine Small	intestine
47	chr5:41214400-41214600	Flanking Active TSS	Liver	Liver
48	chr5:41214600-41215200	Enhancers	Liver	Liver
49	chr5:41215000-41218800	Weak transcription	Fetal Intestine Small	intestine
50	chr5:41215400-41218600	Weak transcription	Fetal Intestine Large	intestine

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