Variant report

Variant	nsv880510
Chromosome Location	chr5:35659239-35709184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:35677686-35677933	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:35668433-35668674	GM12878	blood:	n/a	n/a
3	BATF	chr5:35668416-35668681	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:35699724-35699736	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:35675535-35675851	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr5:35708693-35708709	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:35708704-35708775	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:35692388-35692459	Fibrobl	skin:	n/a	n/a
9	CTCF	chr5:35673341-35673418	ProgFib	skin:	n/a	n/a
10	CTCF	chr5:35708737-35708803	GM19239	blood:	n/a	n/a
11	CUX1	chr5:35668306-35668388	GM12878	blood:	n/a	n/a
12	E2F4	chr5:35703189-35703389	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr5:35693702-35693842	MCF10A-Er-Src	breast:	n/a	n/a
14	EBF1	chr5:35668473-35668787	GM12878	blood:	n/a	n/a
15	EBF1	chr5:35698060-35698255	GM12878	blood:	n/a	n/a
16	FOS	chr5:35669483-35669599	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXA1	chr5:35659703-35660001	T-47D	breast:	n/a	n/a
18	FOXA1	chr5:35683608-35683959	HepG2	liver:	n/a	n/a
19	FOXA1	chr5:35683620-35683899	HepG2	liver:	n/a	n/a
20	GATA1	chr5:35695817-35696136	PBDEFetal	blood:	n/a	n/a
21	GATA2	chr5:35679236-35679781	SH-SY5Y	brain:	n/a	chr5:35679424-35679434
22	GATA2	chr5:35694657-35695154	SH-SY5Y	brain:	n/a	chr5:35695051-35695061
23	GATA3	chr5:35660992-35661040	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr5:35679266-35679611	T-47D	breast:	n/a	chr5:35679424-35679434
25	GATA3	chr5:35694669-35695116	SH-SY5Y	brain:	n/a	chr5:35695051-35695061
26	IKZF1	chr5:35668468-35669257	GM12878	blood:	n/a	n/a
27	JUN	chr5:35686270-35686387	K562	blood:	n/a	n/a
28	JUN	chr5:35674889-35674929	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAFK	chr5:35704264-35704446	HepG2	liver:	n/a	chr5:35704365-35704385
30	MAX	chr5:35702306-35702438	NB4	blood:	n/a	n/a
31	MAZ	chr5:35682969-35683064	HepG2	liver:	n/a	n/a
32	MXI1	chr5:35708672-35708777	HepG2	liver:	n/a	n/a
33	MYC	chr5:35708621-35708715	MCF-7	breast:	n/a	n/a
34	MYC	chr5:35708730-35708743	MCF-7	breast:	n/a	n/a
35	MYC	chr5:35708660-35708725	MCF-7	breast:	n/a	n/a
36	MYC	chr5:35708752-35708781	MCF-7	breast:	n/a	n/a
37	NRF1	chr5:35669182-35669245	GM12878	blood:	n/a	n/a
38	POLR2A	chr5:35698858-35698971	GM12878	blood:	n/a	n/a
39	POLR2A	chr5:35681821-35681900	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr5:35706086-35706185	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr5:35659773-35659973	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr5:35697268-35697302	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr5:35685782-35686082	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr5:35665136-35665645	HL-60	blood:	n/a	n/a
45	POLR2A	chr5:35708584-35708873	Gliobla	brain:	n/a	n/a
46	POLR2A	chr5:35707862-35707884	Gliobla	brain:	n/a	n/a
47	POLR2A	chr5:35665231-35665561	SK-N-MC	brain:	n/a	n/a
48	RFX5	chr5:35684933-35685077	K562	blood:	n/a	n/a
49	SPI1	chr5:35668474-35668710	GM12891	blood:	n/a	n/a
50	SPI1	chr5:35698155-35698463	HL-60	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:35671212-35671262	PFSK-1	brain:	n/a
2	chr5:35671212-35671262	HepG2	liver:	n/a
3	chr5:35671212-35671262	AG10803	skin:	n/a
4	chr5:35671212-35671262	HL-60	blood:	n/a
5	chr5:35671212-35671262	HCF	heart:	n/a
6	chr5:35671212-35671262	Jurkat	blood:	n/a
7	chr5:35671212-35671262	SK-N-SH_RA	brain:	n/a
8	chr5:35671212-35671262	HNPCEpiC	eye:	n/a
9	chr5:35671212-35671262	RPTEC	kidney:	n/a
10	chr5:35671212-35671262	GM19239	blood:	n/a
11	chr5:35671212-35671262	SK-N-MC	brain:	n/a
12	chr5:35671212-35671262	AG09319	gingival:	n/a
13	chr5:35671212-35671262	SAEC	small airway:	n/a
14	chr5:35671212-35671262	BE2_C	brain:	n/a
15	chr5:35671212-35671262	Hepatocyte	liver:	n/a
16	chr5:35671212-35671262	HRCEpiC	kidney:	n/a
17	chr5:35671212-35671262	U87	brain:	n/a
18	chr5:35671212-35671262	HCM	heart:	n/a
19	chr5:35671212-35671262	SK-N-SH	brain:	n/a
20	chr5:35671212-35671262	HMEC	breast:	n/a
21	chr5:35671212-35671262	HCPEpiC	choroid plexus:	n/a
22	chr5:35671212-35671262	NHBE	bronchial:	n/a
23	chr5:35671212-35671262	CMK	blood:	n/a
24	chr5:35671212-35671262	GM12892	blood:	n/a
25	chr5:35671212-35671262	NH-A	brain:	n/a
26	chr5:35671212-35671262	HEEpiC	esophagus:	n/a
27	chr5:35671212-35671262	BJ	skin:	n/a
28	chr5:35671212-35671262	GM06990	blood:	n/a
29	chr5:35671212-35671262	HIPEpiC	eye:	n/a
30	chr5:35671212-35671262	HUVEC	blood vessel:	n/a
31	chr5:35671212-35671262	AG04450	lung:	fetal
32	chr5:35671212-35671262	MCF10A-Er-Src	breast:	n/a
33	chr5:35671212-35671262	AG09309	skin:	n/a
34	chr5:35671212-35671262	PANC-1	pancreas:	n/a
35	chr5:35671212-35671262	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:35671212-35671262	AoSMC	blood vessel:	n/a
37	chr5:35671212-35671262	K562	blood:	n/a
38	chr5:35671212-35671262	ovcar-3	ovarian:	n/a
39	chr5:35671212-35671262	GM12878	blood:	n/a
40	chr5:35671212-35671262	AG04449	skin:	fetal
41	chr5:35671212-35671262	ProgFib	skin:	n/a
42	chr5:35671212-35671262	HRPEpiC	eye:	n/a
43	chr5:35671212-35671262	IMR90	lung:	fetal
44	chr5:35671212-35671262	MCF-7	breast:	n/a
45	chr5:35671212-35671262	HAEpiC	amniotic membrane:	n/a
46	chr5:35671212-35671262	PrEC	prostate:	n/a
47	chr5:35671212-35671262	Hela-S3	cervix:	n/a
48	chr5:35671212-35671262	NB4	blood:	n/a
49	chr5:35671212-35671262	GM12891	blood:	n/a
50	chr5:35671212-35671262	NT2-D1	testis:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:35705714..35707847-chr5:35709289..35711545,3	MCF-7	breast:
2	chr5:35680123..35683959-chr5:35683996..35687791,3	K562	blood:
3	chr5:35680123..35683959-chr5:35683996..35687791,3	K562	blood:
4	chr5:35697548..35700372-chr5:35714640..35716643,2	MCF-7	breast:
5	chr5:35673549..35675188-chr5:35678756..35681423,2	K562	blood:
6	chr5:35673549..35675188-chr5:35678756..35681423,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPSL-1	chr5:35678586-35678811	ENSG00000248969.1
2	lnc-CAPSL-1	chr5:35684082-35684144	ENSG00000248969.1
3	lnc-CAPSL-1	chr5:35698060-35698137	ENSG00000248969.1

No data

Variant related genes	Relation type
SPEF2	TF binding region
SPEF2	CpG island

Extended variants
information (count: 1883 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1883 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16902381	chr5:35659239-35659240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371431624	chr5:35659272-35659273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139099500	chr5:35659277-35659278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200571694	chr5:35659296-35659297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184606856	chr5:35659301-35659302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367661624	chr5:35659308-35659309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367791688	chr5:35659329-35659330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371722581	chr5:35659334-35659335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564934021	chr5:35659342-35659343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9292598	chr5:35659355-35659356	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs138103362	chr5:35659370-35659371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78187528	chr5:35659373-35659374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199973129	chr5:35659452-35659453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs71617726	chr5:35659506-35659507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529574514	chr5:35659517-35659518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs118167953	chr5:35659632-35659633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189223458	chr5:35659636-35659637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537987929	chr5:35659641-35659642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577565375	chr5:35659678-35659679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367584349	chr5:35659689-35659690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557837255	chr5:35659702-35659703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571357867	chr5:35659793-35659794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180756444	chr5:35659828-35659829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553920671	chr5:35659838-35659839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573882792	chr5:35659842-35659843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149537922	chr5:35659843-35659844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200412064	chr5:35659857-35659858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556236759	chr5:35659900-35659901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570145881	chr5:35659936-35659937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570021873	chr5:35659973-35659974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34164245	chr5:35660000-35660001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576117700	chr5:35660011-35660012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373164812	chr5:35660084-35660085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544974501	chr5:35660124-35660125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143997519	chr5:35660152-35660153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572072728	chr5:35660170-35660171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546227504	chr5:35660241-35660242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199525434	chr5:35660264-35660265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148244929	chr5:35660274-35660275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529604624	chr5:35660353-35660354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141294740	chr5:35660376-35660377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74637316	chr5:35660431-35660432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386687167	chr5:35660436-35660437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73750806	chr5:35660437-35660438	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs185475374	chr5:35660472-35660473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12153427	chr5:35660495-35660496	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116812853	chr5:35660581-35660582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188381469	chr5:35660593-35660594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181666693	chr5:35660625-35660626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185853248	chr5:35660643-35660644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
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
prenatal diagnosis	22389664	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	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
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
Medulloblastoma	19270706	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
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35618600-35678000	Weak transcription	Left Ventricle	heart
2	chr5:35630400-35662400	Weak transcription	Aorta	Aorta
3	chr5:35630600-35663400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:35630600-35707600	Weak transcription	Pancreas	Pancrea
5	chr5:35634800-35673200	Weak transcription	Brain Anterior Caudate	brain
6	chr5:35635600-35660400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:35635600-35665400	Weak transcription	Fetal Intestine Small	intestine
8	chr5:35635800-35664000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:35639400-35664600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr5:35640600-35664000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr5:35642600-35673000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr5:35645200-35662200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr5:35645200-35663800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:35645200-35673600	Weak transcription	Fetal Kidney	kidney
15	chr5:35648200-35663400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:35651200-35673000	Weak transcription	Ovary	ovary
17	chr5:35651600-35664600	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr5:35651800-35663400	Weak transcription	Dnd41	blood
19	chr5:35652000-35665000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr5:35656000-35661800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:35656400-35663800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr5:35656400-35670600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:35657200-35660400	Weak transcription	Osteobl	bone
24	chr5:35657400-35673000	Weak transcription	Fetal Heart	heart
25	chr5:35657800-35660200	Enhancers	Primary T cells from cord blood	blood
26	chr5:35658400-35659400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr5:35658600-35664200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:35658800-35660600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:35658800-35665000	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr5:35659200-35659800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr5:35659200-35660200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr5:35659400-35660000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr5:35659800-35664200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr5:35660000-35664800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr5:35660200-35664600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr5:35660400-35660800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr5:35660400-35661000	Enhancers	Osteobl	bone
38	chr5:35660600-35660800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:35660800-35661200	Enhancers	Fetal Lung	lung
40	chr5:35661000-35665200	Weak transcription	Osteobl	bone
41	chr5:35661200-35666800	Weak transcription	Fetal Lung	lung
42	chr5:35663000-35669800	Weak transcription	Liver	Liver
43	chr5:35663400-35664200	Strong transcription	Dnd41	blood
44	chr5:35663400-35664800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:35663400-35664800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr5:35663800-35664800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:35664000-35665200	Weak transcription	Thymus	Thymus
48	chr5:35664000-35665400	Enhancers	Primary hematopoietic stem cells	blood
49	chr5:35664000-35665600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:35664200-35664600	Weak transcription	Dnd41	blood

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