Variant report

Variant	esv2757475
Chromosome Location	chr11:104895876-104979717
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	ARID3A	chr11:104922178-104922768	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104927775-104928650	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104917801-104918523	HepG2	liver:	n/a	n/a
4	ATF3	chr11:104917796-104918302	A549	lung:	n/a	n/a
5	BATF	chr11:104970890-104971077	GM12878	blood:	n/a	n/a
6	BATF	chr11:104948119-104948459	GM12878	blood:	n/a	chr11:104948321-104948332
7	BATF	chr11:104978298-104978484	GM12878	blood:	n/a	chr11:104978391-104978402
8	BATF	chr11:104905693-104906006	GM12878	blood:	n/a	n/a
9	BATF	chr11:104905695-104905944	GM12878	blood:	n/a	n/a
10	BATF	chr11:104915949-104916196	GM12878	blood:	n/a	n/a
11	BCL3	chr11:104917836-104918309	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
12	BCL3	chr11:104917818-104918400	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
13	BHLHE40	chr11:104914225-104914244	GM12878	blood:	n/a	n/a
14	BRCA1	chr11:104913608-104913870	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr11:104917502-104918375	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:104951169-104951316	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:104918828-104918953	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:104978090-104978147	HepG2	liver:	n/a	chr11:104978093-104978104
19	CEBPB	chr11:104979651-104980417	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:104928584-104928787	A549	lung:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
21	CEBPB	chr11:104917718-104918298	A549	lung:	n/a	n/a
22	CEBPB	chr11:104916752-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
23	CEBPB	chr11:104951117-104951358	IMR90	lung:	n/a	n/a
24	CEBPB	chr11:104978050-104978162	IMR90	lung:	n/a	chr11:104978093-104978104
25	CEBPB	chr11:104978051-104978186	Hela-S3	cervix:	n/a	chr11:104978093-104978104
26	CEBPB	chr11:104926001-104926181	IMR90	lung:	n/a	chr11:104926116-104926127 chr11:104926116-104926129 chr11:104926060-104926071
27	CEBPB	chr11:104905749-104906194	HepG2	liver:	n/a	chr11:104905915-104905932 chr11:104905919-104905930
28	CEBPB	chr11:104917907-104918351	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:104914457-104916305	Hela-S3	cervix:	n/a	chr11:104915784-104915797
30	CEBPB	chr11:104916648-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
31	CEBPB	chr11:104948635-104948827	HepG2	liver:	n/a	chr11:104948658-104948669
32	CEBPB	chr11:104916699-104917013	IMR90	lung:	n/a	chr11:104916858-104916869
33	CEBPB	chr11:104917592-104918391	A549	lung:	n/a	n/a
34	CEBPB	chr11:104917671-104918417	IMR90	lung:	n/a	n/a
35	CEBPB	chr11:104925947-104926232	HepG2	liver:	n/a	chr11:104926116-104926127 chr11:104926116-104926129 chr11:104926060-104926071
36	CEBPB	chr11:104905287-104906325	Hela-S3	cervix:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
37	CEBPB	chr11:104915430-104916328	IMR90	lung:	n/a	chr11:104915784-104915797
38	CEBPB	chr11:104917575-104918420	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:104917654-104918310	A549	lung:	n/a	n/a
40	CEBPB	chr11:104913715-104914022	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:104928569-104928699	IMR90	lung:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
42	CEBPB	chr11:104928443-104928828	HepG2	liver:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
43	CEBPB	chr11:104922911-104923232	HepG2	liver:	n/a	chr11:104923066-104923077
44	CEBPB	chr11:104916680-104917050	HepG2	liver:	n/a	chr11:104916858-104916869
45	CEBPB	chr11:104905228-104906180	IMR90	lung:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
46	CEBPB	chr11:104916683-104917034	Hela-S3	cervix:	n/a	chr11:104916858-104916869
47	CEBPD	chr11:104916761-104916943	HepG2	liver:	n/a	n/a
48	CHD2	chr11:104912156-104912184	HepG2	liver:	n/a	n/a
49	CHD2	chr11:104904637-104904755	GM12878	blood:	n/a	n/a
50	CHD2	chr11:104917679-104918334	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104915759-104915809	NB4	blood:	n/a
2	chr11:104906381-104906431	GM06990	blood:	n/a
3	chr11:104973640-104973690	HEEpiC	esophagus:	n/a
4	chr11:104905889-104905939	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:104916075-104916125	NT2-D1	testis:	n/a
6	chr11:104905889-104905939	HRE	kidney:	n/a
7	chr11:104916018-104916068	AG04450	lung:	fetal
8	chr11:104907029-104907079	SK-N-SH_RA	brain:	n/a
9	chr11:104972078-104972128	HMEC	breast:	n/a
10	chr11:104973640-104973690	GM12891	blood:	n/a
11	chr11:104916773-104916823	PrEC	prostate:	n/a
12	chr11:104916331-104916381	GM12878	blood:	n/a
13	chr11:104896587-104896637	IMR90	lung:	fetal
14	chr11:104915759-104915809	HCM	heart:	n/a
15	chr11:104916075-104916125	ECC-1	luminal epithelium:	n/a
16	chr11:104912363-104912413	PFSK-1	brain:	n/a
17	chr11:104972907-104972957	Hepatocyte	liver:	n/a
18	chr11:104966249-104966299	AG04449	skin:	fetal
19	chr11:104972078-104972128	MCF-7	breast:	n/a
20	chr11:104972474-104972524	RPTEC	kidney:	n/a
21	chr11:104972078-104972128	HAEpiC	amniotic membrane:	n/a
22	chr11:104916331-104916381	AG04449	skin:	fetal
23	chr11:104972907-104972957	GM19239	blood:	n/a
24	chr11:104905834-104905884	H1-hESC	embryonic stem cell:	embryo
25	chr11:104916773-104916823	CMK	blood:	n/a
26	chr11:104966249-104966299	HEEpiC	esophagus:	n/a
27	chr11:104916075-104916125	ProgFib	skin:	n/a
28	chr11:104906381-104906431	AG09309	skin:	n/a
29	chr11:104972907-104972957	NB4	blood:	n/a
30	chr11:104905889-104905939	HNPCEpiC	eye:	n/a
31	chr11:104905889-104905939	GM19239	blood:	n/a
32	chr11:104966249-104966299	SAEC	small airway:	n/a
33	chr11:104972135-104972185	Caco-2	colon:	n/a
34	chr11:104972474-104972524	GM12891	blood:	n/a
35	chr11:104905834-104905884	NHBE	bronchial:	n/a
36	chr11:104972135-104972185	AG09319	gingival:	n/a
37	chr11:104972474-104972524	A549	lung:	n/a
38	chr11:104916331-104916381	AG04450	lung:	fetal
39	chr11:104907029-104907079	GM19239	blood:	n/a
40	chr11:104907029-104907079	RPTEC	kidney:	n/a
41	chr11:104905889-104905939	GM12892	blood:	n/a
42	chr11:104915759-104915809	HCF	heart:	n/a
43	chr11:104906381-104906431	A549	lung:	n/a
44	chr11:104915759-104915809	NHDF-neo	bronchial:	n/a
45	chr11:104905834-104905884	Jurkat	blood:	n/a
46	chr11:104906381-104906431	ovcar-3	ovarian:	n/a
47	chr11:104906381-104906431	HNPCEpiC	eye:	n/a
48	chr11:104972135-104972185	GM12891	blood:	n/a
49	chr11:104916773-104916823	ProgFib	skin:	n/a
50	chr11:104905889-104905939	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:
2	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP5-2	chr11:104896235-104896327	NONHSAT023949
2	lnc-CARD16-1	chr11:104904935-104905085	NONHSAT023950
3	lnc-CASP5-2	chr11:104897569-104897899	NONHSAT023949
4	lnc-CARD16-1	chr11:104901581-104902007	NONHSAT023950

Variant related genes	Relation type
CASP1	TF binding region
CARD17	TF binding region
CASP1P2	TF binding region
CASP5	TF binding region
CARD16	TF binding region
CASP1	CpG island
CARD17	CpG island
CASP1P2	CpG island
CASP5	CpG island
CARD16	CpG island

Extended variants
information (count: 3586 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3586 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs507509	chr11:104895876-104895877	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs507438	chr11:104895901-104895902	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541122655	chr11:104895914-104895915	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562297228	chr11:104895956-104895957	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577549398	chr11:104895967-104895968	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559578356	chr11:104895977-104895978	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117777636	chr11:104896001-104896002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563216721	chr11:104896021-104896022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190727112	chr11:104896032-104896033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs504054	chr11:104896047-104896048	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs116738261	chr11:104896057-104896058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184172130	chr11:104896088-104896089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139603415	chr11:104896092-104896093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570823453	chr11:104896095-104896096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539845238	chr11:104896096-104896097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7112592	chr11:104896114-104896115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532970376	chr11:104896132-104896133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569944555	chr11:104896186-104896187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535742884	chr11:104896221-104896222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs483345	chr11:104896226-104896227	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs559992526	chr11:104896245-104896246	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs528978004	chr11:104896330-104896331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60332715	chr11:104896359-104896360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188770918	chr11:104896369-104896370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2509648	chr11:104896375-104896376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557900220	chr11:104896382-104896383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577636197	chr11:104896394-104896395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543408482	chr11:104896503-104896504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192122469	chr11:104896510-104896511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570455302	chr11:104896511-104896512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144216466	chr11:104896516-104896517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs488992	chr11:104896517-104896518	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs56046641	chr11:104896536-104896537	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs551281029	chr11:104896554-104896555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527896734	chr11:104896581-104896582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541199743	chr11:104896600-104896601	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs1790203	chr11:104896613-104896614	Weak transcription Strong transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539454017	chr11:104896723-104896724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553331016	chr11:104896781-104896782	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs74771483	chr11:104896796-104896797	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs202143165	chr11:104896805-104896806	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs569945106	chr11:104896820-104896821	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs1977989	chr11:104896844-104896845	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534811	chr11:104896880-104896881	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs182713127	chr11:104896890-104896891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs476889	chr11:104896893-104896894	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543112326	chr11:104896912-104896913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575932536	chr11:104896936-104896937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148707413	chr11:104896937-104896938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56166030	chr11:104896939-104896940	Weak transcription Strong transcription	n/a	n/a	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:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104887600-104896800	Weak transcription	Placenta	Placenta
2	chr11:104892600-104896400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr11:104892800-104896400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr11:104893200-104896000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:104893600-104896400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr11:104893600-104898800	Weak transcription	NHLF	lung
7	chr11:104893800-104896400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:104893800-104897800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:104893800-104899200	Weak transcription	Fetal Lung	lung
10	chr11:104893800-104899800	Weak transcription	Colonic Mucosa	Colon
11	chr11:104893800-104900200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr11:104894000-104896000	Enhancers	Fetal Intestine Large	intestine
13	chr11:104894000-104896200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:104894000-104896200	Weak transcription	Primary T cells from cord blood	blood
15	chr11:104894000-104896600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr11:104894000-104896800	Weak transcription	Ovary	ovary
17	chr11:104894000-104898400	Weak transcription	Stomach Mucosa	stomach
18	chr11:104894000-104903400	Weak transcription	GM12878-XiMat	blood
19	chr11:104894200-104896200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr11:104894200-104896800	Weak transcription	Left Ventricle	heart
21	chr11:104894200-104896800	Weak transcription	Dnd41	blood
22	chr11:104894200-104898600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:104894200-104899800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:104894200-104904200	Weak transcription	Stomach Smooth Muscle	stomach
25	chr11:104894200-104905600	Weak transcription	Esophagus	oesophagus
26	chr11:104894400-104896600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:104894400-104896800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:104894400-104900400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr11:104894800-104896400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr11:104894800-104897000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr11:104894800-104900200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr11:104894800-104903200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr11:104895000-104896800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:104895000-104899400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr11:104895000-104904200	Weak transcription	Psoas Muscle	Psoas
36	chr11:104895200-104897200	Weak transcription	Small Intestine	intestine
37	chr11:104895200-104898400	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr11:104895200-104898600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr11:104895400-104897000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr11:104895400-104897000	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr11:104895400-104898000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:104895400-104899800	Weak transcription	Spleen	Spleen
43	chr11:104895400-104899800	Weak transcription	NHEK	skin
44	chr11:104895600-104896000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr11:104895600-104896000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:104895600-104896000	Enhancers	Fetal Intestine Small	intestine
47	chr11:104895600-104897600	Strong transcription	Lung	lung
48	chr11:104895600-104902000	Strong transcription	Adipose Nuclei	Adipose
49	chr11:104895800-104896400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr11:104895800-104897800	Strong transcription	Duodenum Mucosa	Duodenum

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