Variant report

Variant	esv1843371
Chromosome Location	chr5:35668036-35706279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 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	chr5:35673341-35673418	ProgFib	skin:	n/a	n/a
7	CTCF	chr5:35692388-35692459	Fibrobl	skin:	n/a	n/a
8	CUX1	chr5:35668306-35668388	GM12878	blood:	n/a	n/a
9	E2F4	chr5:35703189-35703389	MCF10A-Er-Src	breast:	n/a	n/a
10	E2F4	chr5:35693702-35693842	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr5:35668473-35668787	GM12878	blood:	n/a	n/a
12	EBF1	chr5:35698060-35698255	GM12878	blood:	n/a	n/a
13	FOS	chr5:35669483-35669599	MCF10A-Er-Src	breast:	n/a	n/a
14	FOXA1	chr5:35683608-35683959	HepG2	liver:	n/a	n/a
15	FOXA1	chr5:35683620-35683899	HepG2	liver:	n/a	n/a
16	GATA1	chr5:35695817-35696136	PBDEFetal	blood:	n/a	n/a
17	GATA2	chr5:35679236-35679781	SH-SY5Y	brain:	n/a	chr5:35679424-35679434
18	GATA2	chr5:35694657-35695154	SH-SY5Y	brain:	n/a	chr5:35695051-35695061
19	GATA3	chr5:35679266-35679611	T-47D	breast:	n/a	chr5:35679424-35679434
20	GATA3	chr5:35694669-35695116	SH-SY5Y	brain:	n/a	chr5:35695051-35695061
21	IKZF1	chr5:35668468-35669257	GM12878	blood:	n/a	n/a
22	JUN	chr5:35674889-35674929	H1-hESC	embryonic stem cell:	n/a	n/a
23	JUN	chr5:35686270-35686387	K562	blood:	n/a	n/a
24	MAFK	chr5:35704264-35704446	HepG2	liver:	n/a	chr5:35704365-35704385
25	MAX	chr5:35702306-35702438	NB4	blood:	n/a	n/a
26	MAZ	chr5:35682969-35683064	HepG2	liver:	n/a	n/a
27	NRF1	chr5:35669182-35669245	GM12878	blood:	n/a	n/a
28	POLR2A	chr5:35685782-35686082	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr5:35681821-35681900	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr5:35706086-35706185	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr5:35698858-35698971	GM12878	blood:	n/a	n/a
32	POLR2A	chr5:35697268-35697302	MCF10A-Er-Src	breast:	n/a	n/a
33	RFX5	chr5:35684933-35685077	K562	blood:	n/a	n/a
34	SPI1	chr5:35668915-35669258	GM12891	blood:	n/a	chr5:35669062-35669075
35	SPI1	chr5:35698168-35698474	GM12891	blood:	n/a	n/a
36	SPI1	chr5:35668471-35668784	GM12891	blood:	n/a	n/a
37	SPI1	chr5:35698186-35698448	GM12891	blood:	n/a	n/a
38	SPI1	chr5:35668962-35669248	GM12891	blood:	n/a	chr5:35669062-35669075
39	SPI1	chr5:35668474-35668710	GM12891	blood:	n/a	n/a
40	SPI1	chr5:35698155-35698463	HL-60	blood:	n/a	n/a
41	SPI1	chr5:35698172-35698433	GM12878	blood:	n/a	n/a
42	STAT3	chr5:35694473-35694673	MCF10A-Er-Src	breast:	n/a	chr5:35694542-35694562
43	STAT3	chr5:35669439-35669488	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr5:35697917-35697991	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr5:35701531-35701748	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr5:35691228-35691428	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr5:35669408-35669636	MCF10A-Er-Src	breast:	n/a	chr5:35669514-35669525
48	STAT3	chr5:35669356-35669674	MCF10A-Er-Src	breast:	n/a	chr5:35669514-35669525
49	TCF12	chr5:35673227-35673428	GM12878	blood:	n/a	chr5:35673347-35673354
50	ZKSCAN1	chr5:35684724-35684728	Hela-S3	cervix:	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	ProgFib	skin:	n/a
2	chr5:35671212-35671262	AoSMC	blood vessel:	n/a
3	chr5:35671212-35671262	RPTEC	kidney:	n/a
4	chr5:35671212-35671262	AG04449	skin:	fetal
5	chr5:35671212-35671262	HCM	heart:	n/a
6	chr5:35671212-35671262	SK-N-SH	brain:	n/a
7	chr5:35671212-35671262	HMEC	breast:	n/a
8	chr5:35671212-35671262	MCF10A-Er-Src	breast:	n/a
9	chr5:35671212-35671262	HNPCEpiC	eye:	n/a
10	chr5:35671212-35671262	AG04450	lung:	fetal
11	chr5:35671212-35671262	HEK293	kidney:	embryo
12	chr5:35671212-35671262	LNCaP	prostate:	n/a
13	chr5:35671212-35671262	HepG2	liver:	n/a
14	chr5:35671212-35671262	Hela-S3	cervix:	n/a
15	chr5:35671212-35671262	NT2-D1	testis:	n/a
16	chr5:35671212-35671262	CMK	blood:	n/a
17	chr5:35671212-35671262	SK-N-MC	brain:	n/a
18	chr5:35671212-35671262	BJ	skin:	n/a
19	chr5:35671212-35671262	HRPEpiC	eye:	n/a
20	chr5:35671212-35671262	HAEpiC	amniotic membrane:	n/a
21	chr5:35671212-35671262	HCT-116	colon:	n/a
22	chr5:35671212-35671262	HL-60	blood:	n/a
23	chr5:35671212-35671262	GM12891	blood:	n/a
24	chr5:35671212-35671262	HIPEpiC	eye:	n/a
25	chr5:35671212-35671262	IMR90	lung:	fetal
26	chr5:35671212-35671262	NH-A	brain:	n/a
27	chr5:35671212-35671262	AG10803	skin:	n/a
28	chr5:35671212-35671262	PANC-1	pancreas:	n/a
29	chr5:35671212-35671262	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:35671212-35671262	A549	lung:	n/a
31	chr5:35671212-35671262	HRCEpiC	kidney:	n/a
32	chr5:35671212-35671262	Caco-2	colon:	n/a
33	chr5:35671212-35671262	SKMC	muscle:	n/a
34	chr5:35671212-35671262	GM06990	blood:	n/a
35	chr5:35671212-35671262	Jurkat	blood:	n/a
36	chr5:35671212-35671262	NB4	blood:	n/a
37	chr5:35671212-35671262	U87	brain:	n/a
38	chr5:35671212-35671262	HUVEC	blood vessel:	n/a
39	chr5:35671212-35671262	AG09309	skin:	n/a
40	chr5:35671212-35671262	GM12892	blood:	n/a
41	chr5:35671212-35671262	GM12878	blood:	n/a
42	chr5:35671212-35671262	SAEC	small airway:	n/a
43	chr5:35671212-35671262	H1-hESC	embryonic stem cell:	embryo
44	chr5:35671212-35671262	SK-N-SH_RA	brain:	n/a
45	chr5:35671212-35671262	HEEpiC	esophagus:	n/a
46	chr5:35671212-35671262	T-47D	breast:	n/a
47	chr5:35671212-35671262	PrEC	prostate:	n/a
48	chr5:35671212-35671262	AG09319	gingival:	n/a
49	chr5:35671212-35671262	PFSK-1	brain:	n/a
50	chr5:35671212-35671262	BE2_C	brain:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 1415 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2172754	chr5:35668036-35668037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184070499	chr5:35668055-35668056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189671641	chr5:35668086-35668087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80345101	chr5:35668097-35668098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2172755	chr5:35668098-35668099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542901220	chr5:35668120-35668121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73080270	chr5:35668124-35668125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11748781	chr5:35668166-35668167	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369583543	chr5:35668249-35668250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11748763	chr5:35668251-35668252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs10075324	chr5:35668305-35668306	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs116743112	chr5:35668307-35668308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547662440	chr5:35668326-35668327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567459416	chr5:35668337-35668338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529875535	chr5:35668359-35668360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550103821	chr5:35668364-35668365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569823705	chr5:35668371-35668372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538643414	chr5:35668374-35668375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541987960	chr5:35668382-35668383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143244640	chr5:35668398-35668399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368507867	chr5:35668406-35668407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530503442	chr5:35668420-35668421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151213805	chr5:35668485-35668486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35158219	chr5:35668503-35668504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534408938	chr5:35668533-35668534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553984097	chr5:35668570-35668571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550344722	chr5:35668586-35668587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573902712	chr5:35668625-35668626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140394141	chr5:35668650-35668651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185255803	chr5:35668654-35668655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368420392	chr5:35668693-35668694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76553870	chr5:35668720-35668721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190583719	chr5:35668762-35668763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181869933	chr5:35668795-35668796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572545033	chr5:35668863-35668864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7706719	chr5:35668911-35668912	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146972390	chr5:35668925-35668926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186314502	chr5:35668974-35668975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549965973	chr5:35669016-35669017	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs544847145	chr5:35669041-35669042	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs532745375	chr5:35669073-35669074	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs373911715	chr5:35669138-35669139	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552196682	chr5:35669139-35669140	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs115503457	chr5:35669173-35669174	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs189923185	chr5:35669247-35669248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550306695	chr5:35669252-35669253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180673578	chr5:35669329-35669330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546881445	chr5:35669348-35669349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186375850	chr5:35669359-35669360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138104411	chr5:35669414-35669415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35618600-35678000	Weak transcription	Left Ventricle	heart
2	chr5:35630600-35707600	Weak transcription	Pancreas	Pancrea
3	chr5:35634800-35673200	Weak transcription	Brain Anterior Caudate	brain
4	chr5:35642600-35673000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr5:35645200-35673600	Weak transcription	Fetal Kidney	kidney
6	chr5:35651200-35673000	Weak transcription	Ovary	ovary
7	chr5:35656400-35670600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:35657400-35673000	Weak transcription	Fetal Heart	heart
9	chr5:35663000-35669800	Weak transcription	Liver	Liver
10	chr5:35665400-35669000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr5:35665400-35669200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr5:35665400-35671000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr5:35665600-35668200	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr5:35665600-35668600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:35665600-35668600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr5:35665600-35669000	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:35665600-35669000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr5:35665600-35677800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:35665800-35669600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:35665800-35670200	Weak transcription	Dnd41	blood
21	chr5:35666000-35668800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr5:35666000-35669000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr5:35667000-35668600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr5:35667400-35668200	Weak transcription	Primary T cells from cord blood	blood
25	chr5:35667400-35668600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:35667600-35668600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr5:35667800-35672400	Weak transcription	Fetal Lung	lung
28	chr5:35668200-35670800	Enhancers	Primary T cells from cord blood	blood
29	chr5:35668400-35669000	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr5:35668600-35668800	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr5:35668600-35669400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr5:35668600-35671600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:35668600-35675000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:35668600-35675800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr5:35668800-35669200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:35668800-35669200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr5:35668800-35669600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr5:35669000-35669200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr5:35669000-35669800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr5:35669000-35670800	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr5:35669000-35671800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:35669000-35675000	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr5:35669200-35669400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr5:35669200-35670200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr5:35669200-35674800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr5:35669200-35675000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr5:35669400-35669600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr5:35669400-35669600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr5:35669600-35669800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr5:35669600-35670000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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