Variant report

Variant	esv3334824
Chromosome Location	chr11:104776753-104813836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:104778610-104778889	GM12878	blood:	n/a	chr11:104778766-104778777
2	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
3	CEBPB	chr11:104785033-104785128	Hela-S3	cervix:	n/a	chr11:104785067-104785078
4	CEBPB	chr11:104784953-104785176	HepG2	liver:	n/a	chr11:104785067-104785078
5	CEBPB	chr11:104780576-104780776	HepG2	liver:	n/a	chr11:104780651-104780664 chr11:104780651-104780662
6	CHD2	chr11:104796787-104796814	HepG2	liver:	n/a	n/a
7	CTCF	chr11:104805280-104805430	GM12874	blood:	n/a	n/a
8	CTCF	chr11:104778808-104778911	GM19238	blood:	n/a	n/a
9	CTCF	chr11:104778804-104778899	GM19240	blood:	n/a	n/a
10	CTCF	chr11:104797580-104797730	GM12864	blood:	n/a	n/a
11	CTCF	chr11:104778803-104778905	HepG2	liver:	n/a	n/a
12	CTCF	chr11:104776760-104776910	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr11:104778240-104778390	GM12867	blood:	n/a	n/a
14	CTCF	chr11:104778808-104778886	GM19239	blood:	n/a	n/a
15	CTCF	chr11:104789807-104789835	Lung_OC	lung:	n/a	n/a
16	CTCF	chr11:104778816-104778898	GM12892	blood:	n/a	n/a
17	CTCF	chr11:104778200-104778350	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr11:104776640-104776790	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr11:104797685-104797749	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F4	chr11:104813245-104813252	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr11:104788905-104789105	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr11:104788795-104789127	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:104788862-104789127	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXA1	chr11:104796527-104796907	HepG2	liver:	n/a	n/a
25	FOXA1	chr11:104796560-104796871	HepG2	liver:	n/a	n/a
26	FOXA1	chr11:104796564-104796856	HepG2	liver:	n/a	n/a
27	FOXA1	chr11:104796521-104797007	HepG2	liver:	n/a	n/a
28	FOXA2	chr11:104796607-104796854	HepG2	liver:	n/a	n/a
29	JUN	chr11:104788768-104789194	HUVEC	blood vessel:	n/a	n/a
30	MAFF	chr11:104781324-104781367	K562	blood:	n/a	n/a
31	MAFK	chr11:104788844-104789179	IMR90	lung:	n/a	chr11:104789005-104789021
32	MAFK	chr11:104778275-104778643	IMR90	lung:	n/a	n/a
33	MAFK	chr11:104811556-104811603	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAFK	chr11:104788919-104789093	HepG2	liver:	n/a	chr11:104789005-104789021
35	MAFK	chr11:104798723-104798922	HepG2	liver:	n/a	n/a
36	MAZ	chr11:104797857-104797931	HepG2	liver:	n/a	n/a
37	MAZ	chr11:104797800-104798232	IMR90	lung:	n/a	n/a
38	MEF2A	chr11:104805358-104805737	GM12878	blood:	n/a	n/a
39	MYC	chr11:104808166-104808332	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr11:104812858-104813201	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr11:104809423-104809624	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr11:104800704-104800828	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr11:104783136-104783645	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr11:104810811-104814086	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr11:104809983-104810060	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr11:104812124-104812207	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:104812351-104812395	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr11:104776932-104776959	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr11:104812151-104813309	HepG2	liver:	n/a	n/a
50	POLR2A	chr11:104810393-104811985	MCF10A-Er-Src	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104789337-104789387	GM12891	blood:	n/a
2	chr11:104780795-104780845	NT2-D1	testis:	n/a
3	chr11:104780795-104780845	GM12892	blood:	n/a
4	chr11:104789052-104789102	SKMC	muscle:	n/a
5	chr11:104789337-104789387	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:104781259-104781309	HRCEpiC	kidney:	n/a
7	chr11:104778374-104778424	AG04449	skin:	fetal
8	chr11:104778374-104778424	NH-A	brain:	n/a
9	chr11:104789052-104789102	SK-N-MC	brain:	n/a
10	chr11:104779518-104779568	HCF	heart:	n/a
11	chr11:104789337-104789387	HRE	kidney:	n/a
12	chr11:104789052-104789102	HNPCEpiC	eye:	n/a
13	chr11:104780795-104780845	MCF10A-Er-Src	breast:	n/a
14	chr11:104789337-104789387	ECC-1	luminal epithelium:	n/a
15	chr11:104778374-104778424	HCT-116	colon:	n/a
16	chr11:104780795-104780845	RPTEC	kidney:	n/a
17	chr11:104778374-104778424	SAEC	small airway:	n/a
18	chr11:104789337-104789387	Hepatocyte	liver:	n/a
19	chr11:104789337-104789387	AoSMC	blood vessel:	n/a
20	chr11:104781259-104781309	BE2_C	brain:	n/a
21	chr11:104779518-104779568	AG09309	skin:	n/a
22	chr11:104781259-104781309	Jurkat	blood:	n/a
23	chr11:104779518-104779568	AG04450	lung:	fetal
24	chr11:104789052-104789102	SK-N-SH	brain:	n/a
25	chr11:104780795-104780845	AG04449	skin:	fetal
26	chr11:104781259-104781309	AG09309	skin:	n/a
27	chr11:104781259-104781309	PANC-1	pancreas:	n/a
28	chr11:104778374-104778424	HEK293	kidney:	embryo
29	chr11:104779518-104779568	HCT-116	colon:	n/a
30	chr11:104789052-104789102	ovcar-3	ovarian:	n/a
31	chr11:104780712-104780762	GM06990	blood:	n/a
32	chr11:104781259-104781309	HL-60	blood:	n/a
33	chr11:104789052-104789102	AoSMC	blood vessel:	n/a
34	chr11:104789337-104789387	AG04450	lung:	fetal
35	chr11:104789052-104789102	GM12891	blood:	n/a
36	chr11:104779518-104779568	HIPEpiC	eye:	n/a
37	chr11:104780795-104780845	LNCaP	prostate:	n/a
38	chr11:104780712-104780762	GM19239	blood:	n/a
39	chr11:104789052-104789102	SK-N-SH_RA	brain:	n/a
40	chr11:104778374-104778424	HIPEpiC	eye:	n/a
41	chr11:104789052-104789102	Hepatocyte	liver:	n/a
42	chr11:104779518-104779568	U87	brain:	n/a
43	chr11:104778374-104778424	GM19239	blood:	n/a
44	chr11:104779518-104779568	SK-N-SH	brain:	n/a
45	chr11:104779518-104779568	BE2_C	brain:	n/a
46	chr11:104789052-104789102	NHBE	bronchial:	n/a
47	chr11:104778374-104778424	GM12891	blood:	n/a
48	chr11:104781259-104781309	SK-N-SH	brain:	n/a
49	chr11:104779518-104779568	ovcar-3	ovarian:	n/a
50	chr11:104780795-104780845	ProgFib	skin:	n/a

No data

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-3	chr11:104789658-104789800	NONHSAT023943
2	lnc-CASP12-3	chr11:104779562-104779735	NONHSAT023943
3	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
4	lnc-CASP12-3	chr11:104788840-104788902	NR_034079
5	lnc-CASP12-3	chr11:104779562-104779735	NR_034079
6	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944
7	lnc-CASP4-1	chr11:104813600-104813700	NONHSAT023946
8	lnc-CASP12-3	chr11:104788840-104788902	NR_034078
9	lnc-CASP12-3	chr11:104779562-104779735	NR_034078

No data

Variant related genes	Relation type
ENSG00000235505	TF binding region
ENSG00000235505	CpG island

Extended variants
information (count: 1134 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1134 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137960639	chr11:104776786-104776787	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs187691213	chr11:104776796-104776797	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs192223239	chr11:104776825-104776826	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185166461	chr11:104776826-104776827	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs11226548	chr11:104776851-104776852	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs149457854	chr11:104776873-104776874	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547352543	chr11:104776891-104776892	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558375966	chr11:104776897-104776898	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs539376555	chr11:104776945-104776946	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs188434746	chr11:104777055-104777056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569871713	chr11:104777113-104777114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535286712	chr11:104777156-104777157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532705	chr11:104777224-104777225	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs532738	chr11:104777238-104777239	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs11226549	chr11:104777262-104777263	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs143024173	chr11:104777291-104777292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11226550	chr11:104777311-104777312	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs546518504	chr11:104777336-104777337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544229192	chr11:104777358-104777359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138779083	chr11:104777384-104777385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576583110	chr11:104777435-104777436	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs542017953	chr11:104777449-104777450	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561862645	chr11:104777455-104777456	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs372100404	chr11:104777485-104777486	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs192564978	chr11:104777499-104777500	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564172222	chr11:104777531-104777532	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs146251163	chr11:104777609-104777610	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550093095	chr11:104777614-104777615	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115912786	chr11:104777667-104777668	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139326041	chr11:104777672-104777673	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141716748	chr11:104777673-104777674	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534746457	chr11:104777698-104777699	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377652030	chr11:104777706-104777707	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577761012	chr11:104777745-104777746	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79763438	chr11:104777778-104777779	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556825881	chr11:104777784-104777785	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370859826	chr11:104777801-104777802	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576626261	chr11:104777874-104777875	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562726159	chr11:104777895-104777896	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150642128	chr11:104777946-104777947	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56261646	chr11:104777947-104777948	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373101645	chr11:104777982-104777983	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs61890793	chr11:104777988-104777989	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs67307658	chr11:104777989-104777990	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs61890794	chr11:104777990-104777991	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs564723924	chr11:104777992-104777993	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564235829	chr11:104778000-104778001	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs398017415	chr11:104778006-104778007	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375623503	chr11:104778074-104778075	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184492747	chr11:104778101-104778102	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104769200-104777600	Weak transcription	Pancreas	Pancrea
2	chr11:104769200-104778200	Weak transcription	Left Ventricle	heart
3	chr11:104769200-104778800	Weak transcription	NHLF	lung
4	chr11:104769200-104786400	Weak transcription	Lung	lung
5	chr11:104769200-104786600	Weak transcription	Fetal Muscle Leg	muscle
6	chr11:104769200-104787800	Weak transcription	Fetal Lung	lung
7	chr11:104769400-104785400	Weak transcription	Psoas Muscle	Psoas
8	chr11:104769400-104786800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr11:104769600-104785800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr11:104769600-104786800	Weak transcription	Adipose Nuclei	Adipose
11	chr11:104769600-104788000	Weak transcription	Fetal Stomach	stomach
12	chr11:104769800-104777600	Weak transcription	Aorta	Aorta
13	chr11:104770200-104778000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr11:104770400-104777400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr11:104770400-104786600	Weak transcription	Ovary	ovary
16	chr11:104771000-104777400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr11:104772200-104782000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr11:104772400-104777600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:104772400-104778000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr11:104772400-104778600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr11:104772600-104778000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:104772600-104778800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr11:104772600-104783600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:104772800-104778200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr11:104773600-104779800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr11:104773800-104785600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr11:104774200-104777600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:104776400-104787200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:104777400-104778000	Strong transcription	Primary B cells from peripheral blood	blood
30	chr11:104777400-104778200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr11:104777400-104778600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:104777600-104778400	Strong transcription	Aorta	Aorta
33	chr11:104777600-104778400	Strong transcription	Pancreas	Pancrea
34	chr11:104777600-104779000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:104777600-104779200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr11:104778000-104778200	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr11:104778000-104778600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr11:104778000-104779600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:104778000-104779800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:104778200-104778600	Genic enhancers	Primary T cells fromperipheralblood	blood
41	chr11:104778200-104778600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr11:104778200-104778600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr11:104778200-104779000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:104778200-104779000	Enhancers	GM12878-XiMat	blood
45	chr11:104778200-104779200	Strong transcription	Fetal Muscle Trunk	muscle
46	chr11:104778200-104779800	Strong transcription	Left Ventricle	heart
47	chr11:104778400-104786800	Weak transcription	Aorta	Aorta
48	chr11:104778400-104788800	Weak transcription	Pancreas	Pancrea
49	chr11:104778600-104778800	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
50	chr11:104778600-104778800	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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