Variant report

Variant	nsv1042388
Chromosome Location	chr11:104934347-104988325
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	BATF	chr11:104978298-104978484	GM12878	blood:	n/a	chr11:104978391-104978402
2	BATF	chr11:104970890-104971077	GM12878	blood:	n/a	n/a
3	BATF	chr11:104948119-104948459	GM12878	blood:	n/a	chr11:104948321-104948332
4	BRCA1	chr11:104981132-104981302	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr11:104980114-104980416	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:104951117-104951358	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:104978050-104978162	IMR90	lung:	n/a	chr11:104978093-104978104
8	CEBPB	chr11:104983146-104983401	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:104948635-104948827	HepG2	liver:	n/a	chr11:104948658-104948669
10	CEBPB	chr11:104980621-104981623	Hela-S3	cervix:	n/a	chr11:104981527-104981539
11	CEBPB	chr11:104981081-104981355	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:104978051-104978186	Hela-S3	cervix:	n/a	chr11:104978093-104978104
13	CEBPB	chr11:104951169-104951316	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:104978090-104978147	HepG2	liver:	n/a	chr11:104978093-104978104
15	CEBPB	chr11:104979651-104980417	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr11:104980755-104981370	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr11:104948711-104948822	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr11:104979306-104979337	Lung_OC	lung:	n/a	n/a
19	CTCF	chr11:104935783-104935845	GM10248	blood:	n/a	n/a
20	CTCF	chr11:104987320-104987470	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr11:104971768-104971837	GM10266	blood:	n/a	n/a
22	CTCF	chr11:104945420-104945570	BE2_C	brain:	n/a	n/a
23	CTCF	chr11:104972751-104972831	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr11:104943363-104943427	GM13976	blood:	n/a	n/a
25	CTCF	chr11:104945360-104945510	AG09309	skin:	n/a	n/a
26	CTCF	chr11:104963580-104963730	HMEC	breast:	n/a	n/a
27	CTCF	chr11:104941845-104941925	Lung_OC	lung:	n/a	n/a
28	CTCF	chr11:104965975-104966006	GM20000	blood:	n/a	n/a
29	CTCF	chr11:104934583-104934693	LNCaP	prostate:	n/a	n/a
30	CTCF	chr11:104963680-104963830	HMEC	breast:	n/a	n/a
31	CTCF	chr11:104963760-104963910	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr11:104945394-104945576	H1-hESC	embryonic stem cell:	n/a	n/a
33	E2F4	chr11:104945873-104946021	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr11:104985599-104985639	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr11:104984402-104984512	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr11:104946814-104946837	GM12878	blood:	n/a	chr11:104946815-104946826
37	EP300	chr11:104980674-104981354	Hela-S3	cervix:	n/a	chr11:104981322-104981336 chr11:104981324-104981338 chr11:104981328-104981342 chr11:104981052-104981062
38	EP300	chr11:104980066-104980404	Hela-S3	cervix:	n/a	n/a
39	FOS	chr11:104948241-104948837	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:104980126-104980399	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:104970874-104971326	HUVEC	blood vessel:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
42	FOS	chr11:104970870-104971415	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
43	FOS	chr11:104948262-104948729	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:104971878-104972346	MCF10A-Er-Src	breast:	n/a	chr11:104971936-104971945
45	FOS	chr11:104942222-104942367	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr11:104984366-104984632	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr11:104970835-104971425	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
48	FOS	chr11:104942187-104942387	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:104984337-104984625	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:104984339-104984638	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104973640-104973690	HepG2	liver:	n/a
2	chr11:104966249-104966299	GM12878	blood:	n/a
3	chr11:104972907-104972957	HCT-116	colon:	n/a
4	chr11:104966249-104966299	HAEpiC	amniotic membrane:	n/a
5	chr11:104972907-104972957	AG09309	skin:	n/a
6	chr11:104972135-104972185	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:104972135-104972185	T-47D	breast:	n/a
8	chr11:104966249-104966299	MCF-7	breast:	n/a
9	chr11:104972474-104972524	SAEC	small airway:	n/a
10	chr11:104972078-104972128	ovcar-3	ovarian:	n/a
11	chr11:104972135-104972185	RPTEC	kidney:	n/a
12	chr11:104972078-104972128	HMEC	breast:	n/a
13	chr11:104972907-104972957	HRCEpiC	kidney:	n/a
14	chr11:104972078-104972128	HUVEC	blood vessel:	n/a
15	chr11:104966249-104966299	BJ	skin:	n/a
16	chr11:104972078-104972128	Hela-S3	cervix:	n/a
17	chr11:104966249-104966299	BE2_C	brain:	n/a
18	chr11:104972474-104972524	HCPEpiC	choroid plexus:	n/a
19	chr11:104972135-104972185	HCM	heart:	n/a
20	chr11:104973640-104973690	HEK293	kidney:	embryo
21	chr11:104973640-104973690	T-47D	breast:	n/a
22	chr11:104972907-104972957	ProgFib	skin:	n/a
23	chr11:104972907-104972957	AG04450	lung:	fetal
24	chr11:104972135-104972185	BJ	skin:	n/a
25	chr11:104973640-104973690	K562	blood:	n/a
26	chr11:104972474-104972524	HRE	kidney:	n/a
27	chr11:104972078-104972128	HEEpiC	esophagus:	n/a
28	chr11:104966249-104966299	HCF	heart:	n/a
29	chr11:104972135-104972185	U87	brain:	n/a
30	chr11:104973640-104973690	PFSK-1	brain:	n/a
31	chr11:104972907-104972957	SK-N-SH_RA	brain:	n/a
32	chr11:104972135-104972185	H1-hESC	embryonic stem cell:	embryo
33	chr11:104973640-104973690	HCF	heart:	n/a
34	chr11:104972135-104972185	Hepatocyte	liver:	n/a
35	chr11:104966249-104966299	U87	brain:	n/a
36	chr11:104966249-104966299	AG10803	skin:	n/a
37	chr11:104972907-104972957	GM12892	blood:	n/a
38	chr11:104972135-104972185	K562	blood:	n/a
39	chr11:104966249-104966299	AG09309	skin:	n/a
40	chr11:104972474-104972524	BJ	skin:	n/a
41	chr11:104972135-104972185	AG09309	skin:	n/a
42	chr11:104973640-104973690	U87	brain:	n/a
43	chr11:104972474-104972524	SK-N-SH	brain:	n/a
44	chr11:104972078-104972128	BJ	skin:	n/a
45	chr11:104973640-104973690	BJ	skin:	n/a
46	chr11:104972474-104972524	Caco-2	colon:	n/a
47	chr11:104966249-104966299	PFSK-1	brain:	n/a
48	chr11:104972474-104972524	NHDF-neo	bronchial:	n/a
49	chr11:104972078-104972128	NHDF-neo	bronchial:	n/a
50	chr11:104972907-104972957	NHDF-neo	bronchial:	n/a

Variant related genes	Relation type
CASP1	TF binding region
CARD16	TF binding region
CARD17	TF binding region
CASP1P2	TF binding region
CASP1	CpG island
CARD16	CpG island
CARD17	CpG island
CASP1P2	CpG island

Extended variants
information (count: 2041 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2041 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568889135	chr11:104934355-104934356	Active TSS Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs373834115	chr11:104934357-104934358	Active TSS Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569463955	chr11:104934384-104934385	Active TSS Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs1785871	chr11:104934390-104934391	Active TSS Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs567857588	chr11:104934401-104934402	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs536888951	chr11:104934427-104934428	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs553157807	chr11:104934449-104934450	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573054140	chr11:104934459-104934460	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184183896	chr11:104934479-104934480	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs558591709	chr11:104934488-104934489	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575628141	chr11:104934494-104934495	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544279108	chr11:104934546-104934547	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs189405806	chr11:104934570-104934571	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs180959177	chr11:104934674-104934675	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4106100	chr11:104934691-104934692	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185835498	chr11:104934706-104934707	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560413312	chr11:104934711-104934712	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532315250	chr11:104934777-104934778	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545956612	chr11:104934778-104934779	Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190933913	chr11:104934812-104934813	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531382530	chr11:104934829-104934830	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367879589	chr11:104934862-104934863	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113282289	chr11:104934885-104934886	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547865698	chr11:104934909-104934910	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568005567	chr11:104934921-104934922	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530328870	chr11:104934938-104934939	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546861699	chr11:104934968-104934969	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17103670	chr11:104934992-104934993	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs472886	chr11:104935003-104935004	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs569244551	chr11:104935009-104935010	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145837578	chr11:104935017-104935018	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554669485	chr11:104935034-104935035	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145467403	chr11:104935053-104935054	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374653451	chr11:104935088-104935089	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540552005	chr11:104935139-104935140	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532831064	chr11:104935141-104935142	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181983544	chr11:104935165-104935166	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11226603	chr11:104935222-104935223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367779434	chr11:104935234-104935235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551919781	chr11:104935245-104935246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148812231	chr11:104935250-104935251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559413561	chr11:104935291-104935292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528057320	chr11:104935292-104935293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs486123	chr11:104935330-104935331	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs537933508	chr11:104935335-104935336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11226604	chr11:104935420-104935421	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs485175	chr11:104935425-104935426	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186254461	chr11:104935430-104935431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143627826	chr11:104935450-104935451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34943448	chr11:104935465-104935466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104927000-104936200	Weak transcription	Small Intestine	intestine
2	chr11:104931000-104936800	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr11:104931600-104936200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr11:104932200-104936800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr11:104933600-104936400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:104934000-104934400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:104934000-104934600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:104934000-104934800	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr11:104934200-104934400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:104934200-104934400	Active TSS	HMEC	breast
11	chr11:104934400-104934600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:104934400-104934600	Flanking Active TSS	HMEC	breast
13	chr11:104934400-104935000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:104934400-104935200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:104934400-104935200	Enhancers	NHEK	skin
16	chr11:104934600-104934800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:104934600-104935000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:104934600-104935000	Enhancers	HMEC	breast
19	chr11:104934800-104935200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr11:104935200-104936400	Weak transcription	NHEK	skin
21	chr11:104935200-104938200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:104935200-104941200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:104936200-104939000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr11:104936200-104939600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr11:104936400-104937200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr11:104936800-104937000	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr11:104936800-104937000	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr11:104937000-104937400	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr11:104937000-104937400	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr11:104937200-104937600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:104937400-104938600	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr11:104937400-104938800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr11:104937600-104939800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:104938200-104938400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr11:104938200-104938600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:104938200-104941800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:104938600-104939600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr11:104938600-104939600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:104938600-104939600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr11:104938800-104939400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr11:104939000-104940600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr11:104939400-104940000	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr11:104939600-104939800	Enhancers	Primary T cells fromperipheralblood	blood
44	chr11:104939600-104940000	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr11:104939600-104940200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:104939600-104940400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:104939600-104940400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr11:104939600-104941000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:104939600-104941000	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr11:104939800-104940200	Weak transcription	Primary T cells fromperipheralblood	blood

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