Variant report

Variant	nsv8871
Chromosome Location	chr11:104941750-104973508
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	chr11:104970890-104971077	GM12878	blood:	n/a	n/a
2	BATF	chr11:104948119-104948459	GM12878	blood:	n/a	chr11:104948321-104948332
3	CEBPB	chr11:104948635-104948827	HepG2	liver:	n/a	chr11:104948658-104948669
4	CEBPB	chr11:104951117-104951358	IMR90	lung:	n/a	n/a
5	CEBPB	chr11:104951169-104951316	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr11:104963680-104963830	HMEC	breast:	n/a	n/a
7	CTCF	chr11:104972751-104972831	Spleen_OC	spleen:	n/a	n/a
8	CTCF	chr11:104945420-104945570	BE2_C	brain:	n/a	n/a
9	CTCF	chr11:104945394-104945576	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:104965975-104966006	GM20000	blood:	n/a	n/a
11	CTCF	chr11:104963580-104963730	HMEC	breast:	n/a	n/a
12	CTCF	chr11:104971768-104971837	GM10266	blood:	n/a	n/a
13	CTCF	chr11:104945360-104945510	AG09309	skin:	n/a	n/a
14	CTCF	chr11:104943363-104943427	GM13976	blood:	n/a	n/a
15	CTCF	chr11:104948711-104948822	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr11:104941845-104941925	Lung_OC	lung:	n/a	n/a
17	CTCF	chr11:104963760-104963910	HPAF	blood vessel:	n/a	n/a
18	E2F4	chr11:104945873-104946021	MCF10A-Er-Src	breast:	n/a	n/a
19	EBF1	chr11:104946814-104946837	GM12878	blood:	n/a	chr11:104946815-104946826
20	FOS	chr11:104970836-104971491	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
21	FOS	chr11:104948262-104948729	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr11:104944266-104944785	HUVEC	blood vessel:	n/a	n/a
23	FOS	chr11:104972042-104972303	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr11:104972012-104972419	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr11:104971878-104972346	MCF10A-Er-Src	breast:	n/a	chr11:104971936-104971945
26	FOS	chr11:104942222-104942367	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr11:104963677-104964022	HUVEC	blood vessel:	n/a	chr11:104963836-104963847 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
28	FOS	chr11:104963304-104963982	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
29	FOS	chr11:104963304-104963925	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
30	FOS	chr11:104970874-104971326	HUVEC	blood vessel:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
31	FOS	chr11:104942187-104942387	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr11:104948241-104948837	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr11:104970870-104971415	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
34	FOS	chr11:104942242-104942452	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr11:104948211-104948907	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:104971940-104972376	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:104963328-104963986	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
38	FOS	chr11:104948928-104949030	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:104970925-104971329	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
40	FOS	chr11:104970835-104971425	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
41	FOXA2	chr11:104960656-104960851	HepG2	liver:	n/a	n/a
42	GATA2	chr11:104963362-104963700	SH-SY5Y	brain:	n/a	chr11:104963445-104963455
43	GATA2	chr11:104970412-104971122	HUVEC	blood vessel:	n/a	chr11:104970654-104970665 chr11:104970652-104970661 chr11:104971022-104971032 chr11:104970575-104970585
44	GATA3	chr11:104963287-104963717	SH-SY5Y	brain:	n/a	chr11:104963445-104963455
45	GATA3	chr11:104963367-104963635	MCF-7	breast:	n/a	chr11:104963445-104963455
46	JUN	chr11:104945011-104945062	K562	blood:	n/a	n/a
47	JUND	chr11:104971147-104971315	H1-hESC	embryonic stem cell:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
48	MAFF	chr11:104947432-104947580	HepG2	liver:	n/a	n/a
49	MAFK	chr11:104947352-104947628	HepG2	liver:	n/a	n/a
50	MAFK	chr11:104947451-104947500	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104972907-104972957	HL-60	blood:	n/a
2	chr11:104972907-104972957	Jurkat	blood:	n/a
3	chr11:104966249-104966299	HEK293	kidney:	embryo
4	chr11:104972907-104972957	HAEpiC	amniotic membrane:	n/a
5	chr11:104966249-104966299	PANC-1	pancreas:	n/a
6	chr11:104966249-104966299	HNPCEpiC	eye:	n/a
7	chr11:104972135-104972185	K562	blood:	n/a
8	chr11:104972135-104972185	RPTEC	kidney:	n/a
9	chr11:104972907-104972957	GM12891	blood:	n/a
10	chr11:104972474-104972524	HEEpiC	esophagus:	n/a
11	chr11:104972135-104972185	GM12892	blood:	n/a
12	chr11:104972907-104972957	HEEpiC	esophagus:	n/a
13	chr11:104972135-104972185	NH-A	brain:	n/a
14	chr11:104972474-104972524	HRE	kidney:	n/a
15	chr11:104966249-104966299	Caco-2	colon:	n/a
16	chr11:104972474-104972524	HRPEpiC	eye:	n/a
17	chr11:104966249-104966299	K562	blood:	n/a
18	chr11:104972474-104972524	HepG2	liver:	n/a
19	chr11:104972907-104972957	HCPEpiC	choroid plexus:	n/a
20	chr11:104972907-104972957	RPTEC	kidney:	n/a
21	chr11:104972135-104972185	HNPCEpiC	eye:	n/a
22	chr11:104972474-104972524	HCM	heart:	n/a
23	chr11:104972474-104972524	NB4	blood:	n/a
24	chr11:104972078-104972128	BE2_C	brain:	n/a
25	chr11:104972907-104972957	HRE	kidney:	n/a
26	chr11:104972907-104972957	HCM	heart:	n/a
27	chr11:104966249-104966299	HepG2	liver:	n/a
28	chr11:104972078-104972128	SKMC	muscle:	n/a
29	chr11:104972907-104972957	HepG2	liver:	n/a
30	chr11:104966249-104966299	HEEpiC	esophagus:	n/a
31	chr11:104972474-104972524	BE2_C	brain:	n/a
32	chr11:104966249-104966299	ProgFib	skin:	n/a
33	chr11:104972078-104972128	HEK293	kidney:	embryo
34	chr11:104972474-104972524	PANC-1	pancreas:	n/a
35	chr11:104972135-104972185	HCPEpiC	choroid plexus:	n/a
36	chr11:104972078-104972128	NHBE	bronchial:	n/a
37	chr11:104972474-104972524	ProgFib	skin:	n/a
38	chr11:104972474-104972524	BJ	skin:	n/a
39	chr11:104972907-104972957	HRCEpiC	kidney:	n/a
40	chr11:104972135-104972185	H1-hESC	embryonic stem cell:	embryo
41	chr11:104972907-104972957	BE2_C	brain:	n/a
42	chr11:104972474-104972524	HEK293	kidney:	embryo
43	chr11:104972474-104972524	AoSMC	blood vessel:	n/a
44	chr11:104972135-104972185	HRCEpiC	kidney:	n/a
45	chr11:104972907-104972957	SK-N-SH_RA	brain:	n/a
46	chr11:104972135-104972185	HRE	kidney:	n/a
47	chr11:104972078-104972128	PFSK-1	brain:	n/a
48	chr11:104972135-104972185	ECC-1	luminal epithelium:	n/a
49	chr11:104972078-104972128	NB4	blood:	n/a
50	chr11:104972474-104972524	RPTEC	kidney:	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: 1200 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1200 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556025773	chr11:104941773-104941774	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs556020493	chr11:104941780-104941781	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs536431372	chr11:104941820-104941821	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs184792953	chr11:104941850-104941851	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs374970542	chr11:104941851-104941852	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150933319	chr11:104941875-104941876	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs537886542	chr11:104941885-104941886	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564403007	chr11:104941908-104941909	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs478900	chr11:104941974-104941975	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543462123	chr11:104941976-104941977	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs563295241	chr11:104942046-104942047	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs529171582	chr11:104942082-104942083	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569853446	chr11:104942086-104942087	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs143529017	chr11:104942094-104942095	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs528250157	chr11:104942098-104942099	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369381907	chr11:104942102-104942103	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs551499126	chr11:104942113-104942114	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs571243126	chr11:104942132-104942133	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs188399692	chr11:104942162-104942163	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs111818379	chr11:104942169-104942170	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs567245177	chr11:104942170-104942171	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs536174178	chr11:104942180-104942181	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs556081836	chr11:104942191-104942192	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs146753112	chr11:104942195-104942196	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs566291803	chr11:104942197-104942198	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs60902592	chr11:104942215-104942216	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs150344097	chr11:104942227-104942228	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs578035727	chr11:104942244-104942245	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs543483094	chr11:104942278-104942279	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs556950342	chr11:104942279-104942280	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs573681627	chr11:104942312-104942313	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs542539052	chr11:104942315-104942316	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs559381884	chr11:104942316-104942317	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528326754	chr11:104942323-104942324	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs35076065	chr11:104942335-104942336	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs138018928	chr11:104942359-104942360	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs149168678	chr11:104942362-104942363	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs530543313	chr11:104942377-104942378	Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs550662805	chr11:104942412-104942413	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567306382	chr11:104942431-104942432	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529692917	chr11:104942432-104942433	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549745422	chr11:104942448-104942449	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs566233340	chr11:104942452-104942453	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535275709	chr11:104942459-104942460	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs143269235	chr11:104942467-104942468	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs191349045	chr11:104942480-104942481	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs537181926	chr11:104942482-104942483	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537307096	chr11:104942497-104942498	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368236869	chr11:104942500-104942501	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373280386	chr11:104942538-104942539	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104938200-104941800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:104940200-104942400	Active TSS	Primary T cells fromperipheralblood	blood
3	chr11:104940800-104943200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:104941000-104941800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:104941000-104942000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr11:104941000-104942200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
7	chr11:104941000-104942600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:104941000-104942600	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr11:104941000-104942600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr11:104941200-104942000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:104941200-104942200	Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr11:104941200-104942400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:104941200-104942400	Enhancers	Placenta	Placenta
14	chr11:104941400-104942000	Active TSS	Primary T killer memory cells from peripheral blood	blood
15	chr11:104941400-104942200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
16	chr11:104941400-104942400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
17	chr11:104941400-104942400	Flanking Active TSS	NHEK	skin
18	chr11:104941400-104942600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:104941400-104942600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr11:104941600-104941800	Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr11:104941600-104941800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr11:104941600-104941800	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr11:104941600-104942200	Active TSS	Primary T helper naive cells from peripheral blood	blood
24	chr11:104941600-104942400	Enhancers	HMEC	breast
25	chr11:104941800-104942000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr11:104941800-104942000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr11:104941800-104942000	Enhancers	Duodenum Mucosa	Duodenum
28	chr11:104941800-104942200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr11:104941800-104942200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:104941800-104942200	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr11:104942000-104942200	Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr11:104942000-104942200	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr11:104942000-104942200	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr11:104942000-104942400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:104942000-104942400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:104942000-104942600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr11:104942200-104942400	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr11:104942200-104942400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:104942200-104942400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr11:104942200-104942400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:104942200-104942400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr11:104942400-104942600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr11:104942400-104942600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr11:104942400-104942600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr11:104942400-104942600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr11:104942400-104942600	Enhancers	NHEK	skin
47	chr11:104942400-104943000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:104942400-104947600	Weak transcription	HMEC	breast
49	chr11:104942400-104948000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr11:104942600-104943000	Enhancers	Monocytes-CD14+_RO01746	blood

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