Variant report

Variant	esv2830219
Chromosome Location	chr11:101319531-101382967
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	chr11:101335227-101335368	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:101327642-101327769	HepG2	liver:	n/a	n/a
3	ATF1	chr11:101352514-101352557	K562	blood:	n/a	n/a
4	BRCA1	chr11:101349905-101349951	HepG2	liver:	n/a	n/a
5	BRCA1	chr11:101339384-101339392	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:101329812-101330088	HCT-116	colon:	n/a	n/a
7	CEBPB	chr11:101358457-101358896	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:101349926-101350046	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:101341197-101341572	IMR90	lung:	n/a	chr11:101341377-101341388
10	CEBPB	chr11:101335219-101335438	HepG2	liver:	n/a	chr11:101335331-101335342
11	CEBPB	chr11:101341270-101341507	K562	blood:	n/a	chr11:101341377-101341388
12	CEBPB	chr11:101341262-101341509	ECC-1	luminal epithelium:	n/a	chr11:101341377-101341388
13	CEBPB	chr11:101379723-101379937	HepG2	liver:	n/a	chr11:101379791-101379802 chr11:101379790-101379803
14	CEBPB	chr11:101341248-101341495	H1-hESC	embryonic stem cell:	n/a	chr11:101341377-101341388
15	CEBPB	chr11:101341220-101341454	Hela-S3	cervix:	n/a	chr11:101341377-101341388
16	CEBPB	chr11:101341250-101341517	HepG2	liver:	n/a	chr11:101341377-101341388
17	CEBPB	chr11:101341221-101341533	A549	lung:	n/a	chr11:101341377-101341388
18	CTCF	chr11:101327560-101327710	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr11:101327641-101327811	GM12878	blood:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
20	CTCF	chr11:101348620-101348770	HEEpiC	esophagus:	n/a	chr11:101348673-101348691 chr11:101348675-101348688
21	CTCF	chr11:101327540-101327690	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr11:101327620-101327788	LNCaP	prostate:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
23	CTCF	chr11:101349900-101350050	GM12869	blood:	n/a	n/a
24	CTCF	chr11:101327320-101327470	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr11:101327180-101327330	AG10803	skin:	n/a	n/a
26	CTCF	chr11:101327560-101327710	HFF	foreskin:	n/a	n/a
27	CTCF	chr11:101327692-101327715	GM13976	blood:	n/a	n/a
28	CTCF	chr11:101327660-101327810	GM12865	blood:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
29	CTCF	chr11:101348520-101348670	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr11:101327680-101327830	HA-sp	spinal cord:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
31	CTCF	chr11:101327660-101327810	GM12873	blood:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
32	CTCF	chr11:101327640-101327790	RPTEC	kidney:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
33	CTCF	chr11:101348620-101348770	HRPEpiC	eye:	n/a	chr11:101348673-101348691 chr11:101348675-101348688
34	CTCF	chr11:101327660-101327810	AG04450	lung:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
35	CTCF	chr11:101327640-101327790	HPF	lung:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
36	CTCF	chr11:101327598-101327847	HCT-116	colon:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
37	CTCF	chr11:101348580-101348730	HMEC	breast:	n/a	chr11:101348673-101348691 chr11:101348675-101348688
38	CTCF	chr11:101327621-101327833	Lung_OC	lung:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
39	CTCF	chr11:101327640-101327790	NHEK	skin:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
40	CTCF	chr11:101327740-101327890	AG04450	lung:	n/a	n/a
41	CTCF	chr11:101367076-101367152	GM12878	blood:	n/a	chr11:101367108-101367129 chr11:101367106-101367124 chr11:101367107-101367123 chr11:101367111-101367121
42	CTCF	chr11:101327660-101327810	HCM	heart:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
43	CTCF	chr11:101376980-101377130	HMF	breast:	n/a	n/a
44	CTCF	chr11:101327572-101327884	A549	lung:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
45	CTCF	chr11:101327462-101328054	HCT-116	colon:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
46	CTCF	chr11:101342086-101342148	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr11:101327548-101327907	GM12878	blood:	n/a	chr11:101327721-101327742 chr11:101327719-101327737
48	CTCF	chr11:101348660-101348810	Hela-S3	cervix:	n/a	chr11:101348673-101348691 chr11:101348675-101348688
49	CTCF	chr11:101327760-101327910	HAc	cerebellar:	n/a	n/a
50	CTCF	chr11:101327620-101327770	Caco-2	colon:	n/a	chr11:101327721-101327742 chr11:101327719-101327737

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:101341554-101341604	GM06990	blood:	n/a
2	chr11:101341554-101341604	GM12892	blood:	n/a
3	chr11:101341554-101341604	GM19239	blood:	n/a
4	chr11:101323578-101323628	HCF	heart:	n/a
5	chr11:101323578-101323628	GM12878	blood:	n/a
6	chr11:101323578-101323628	Hepatocyte	liver:	n/a
7	chr11:101341554-101341604	HCM	heart:	n/a
8	chr11:101341554-101341604	HEK293	kidney:	embryo
9	chr11:101341554-101341604	HMEC	breast:	n/a
10	chr11:101341554-101341604	SAEC	small airway:	n/a
11	chr11:101323578-101323628	HRCEpiC	kidney:	n/a
12	chr11:101341554-101341604	NHDF-neo	bronchial:	n/a
13	chr11:101323578-101323628	NH-A	brain:	n/a
14	chr11:101341554-101341604	HEEpiC	esophagus:	n/a
15	chr11:101323578-101323628	T-47D	breast:	n/a
16	chr11:101341554-101341604	RPTEC	kidney:	n/a
17	chr11:101341554-101341604	Jurkat	blood:	n/a
18	chr11:101341554-101341604	AG04449	skin:	fetal
19	chr11:101323578-101323628	NHBE	bronchial:	n/a
20	chr11:101341554-101341604	NT2-D1	testis:	n/a
21	chr11:101341554-101341604	BJ	skin:	n/a
22	chr11:101341554-101341604	SK-N-SH	brain:	n/a
23	chr11:101341554-101341604	AG04450	lung:	fetal
24	chr11:101323578-101323628	HUVEC	blood vessel:	n/a
25	chr11:101341554-101341604	Hela-S3	cervix:	n/a
26	chr11:101323578-101323628	PFSK-1	brain:	n/a
27	chr11:101341554-101341604	BE2_C	brain:	n/a
28	chr11:101323578-101323628	BJ	skin:	n/a
29	chr11:101341554-101341604	HepG2	liver:	n/a
30	chr11:101323578-101323628	Caco-2	colon:	n/a
31	chr11:101341554-101341604	HRPEpiC	eye:	n/a
32	chr11:101323578-101323628	SK-N-SH	brain:	n/a
33	chr11:101323578-101323628	HL-60	blood:	n/a
34	chr11:101341554-101341604	PrEC	prostate:	n/a
35	chr11:101341554-101341604	PANC-1	pancreas:	n/a
36	chr11:101323578-101323628	SAEC	small airway:	n/a
37	chr11:101323578-101323628	ovcar-3	ovarian:	n/a
38	chr11:101341554-101341604	HAEpiC	amniotic membrane:	n/a
39	chr11:101323578-101323628	HIPEpiC	eye:	n/a
40	chr11:101341554-101341604	ECC-1	luminal epithelium:	n/a
41	chr11:101341554-101341604	NHBE	bronchial:	n/a
42	chr11:101323578-101323628	NT2-D1	testis:	n/a
43	chr11:101341554-101341604	HRCEpiC	kidney:	n/a
44	chr11:101323578-101323628	HAEpiC	amniotic membrane:	n/a
45	chr11:101341554-101341604	U87	brain:	n/a
46	chr11:101341554-101341604	HCPEpiC	choroid plexus:	n/a
47	chr11:101323578-101323628	HEEpiC	esophagus:	n/a
48	chr11:101323578-101323628	BE2_C	brain:	n/a
49	chr11:101323578-101323628	HCM	heart:	n/a
50	chr11:101323578-101323628	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:101311732..101314257-chr11:101315971..101319551,3	MCF-7	breast:
2	chr11:101373238..101376109-chr11:101378947..101380579,2	K562	blood:
3	chr11:101315303..101317533-chr11:101320220..101323085,2	MCF-7	breast:
4	chr11:101357724..101358302-chr4:125044591..125045215,2	MCF-7	breast:
5	chr11:101367288..101368830-chr11:101394227..101396283,2	K562	blood:
6	chr11:101327259..101328354-chr11:101718588..101719686,4	MCF-7	breast:
7	chr11:101310309..101314049-chr11:101319815..101323131,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGR-5	chr11:101324372-101324456	NONHSAT023857
2	lnc-PGR-5	chr11:101325749-101326308	NONHSAT023857

Variant related genes	Relation type
TRPC6	TF binding region
TRPC6	CpG island
ENSG00000137672	chromatin interactions

Extended variants
information (count: 2842 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2842 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3824933	chr11:101319531-101319532	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549679434	chr11:101319539-101319540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548739503	chr11:101319541-101319542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569484890	chr11:101319556-101319557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144970121	chr11:101319614-101319615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555029589	chr11:101319619-101319620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565804916	chr11:101319627-101319628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534317588	chr11:101319712-101319713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557687011	chr11:101319713-101319714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531738085	chr11:101319726-101319727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577574330	chr11:101319731-101319732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74440503	chr11:101319767-101319768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4132959	chr11:101319788-101319789	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs533158376	chr11:101319806-101319807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182074608	chr11:101319813-101319814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543284079	chr11:101319833-101319834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186364960	chr11:101319849-101319850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528540826	chr11:101319891-101319892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368721107	chr11:101319923-101319924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374493072	chr11:101319946-101319947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565246892	chr11:101319963-101319964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73587962	chr11:101319964-101319965	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs555404879	chr11:101320017-101320018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566564741	chr11:101320171-101320172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145807712	chr11:101320238-101320239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569648625	chr11:101320328-101320329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529042206	chr11:101320374-101320375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202073615	chr11:101320405-101320406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs71056603	chr11:101320444-101320445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55788517	chr11:101320446-101320447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369183107	chr11:101320450-101320451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151319602	chr11:101320462-101320463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549204810	chr11:101320489-101320490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562278379	chr11:101320534-101320535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34388292	chr11:101320541-101320542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148982893	chr11:101320571-101320572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534671208	chr11:101320644-101320645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557592208	chr11:101320687-101320688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571203272	chr11:101320699-101320700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191312039	chr11:101320701-101320702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143065691	chr11:101320747-101320748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7113655	chr11:101320748-101320749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543347287	chr11:101320823-101320824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115777057	chr11:101320862-101320863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114610738	chr11:101320896-101320897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545455118	chr11:101320917-101320918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183499851	chr11:101320937-101320938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188608987	chr11:101320980-101320981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114727009	chr11:101321049-101321050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148224831	chr11:101321059-101321060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Melanoma	22183965	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
Myelofibrosis	22110671	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
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101311600-101319600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr11:101314400-101321200	Enhancers	NHDF-Ad	bronchial
3	chr11:101314400-101352800	Weak transcription	Aorta	Aorta
4	chr11:101316400-101330000	Weak transcription	Fetal Lung	lung
5	chr11:101317400-101320200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:101317400-101324400	Weak transcription	NH-A	brain
7	chr11:101317600-101320600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:101317600-101322000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr11:101317600-101324000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:101318400-101319600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:101318400-101319800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:101318800-101324200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr11:101318800-101327800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:101319400-101320000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:101319400-101320000	Enhancers	Ovary	ovary
16	chr11:101319600-101319800	Enhancers	HSMM	muscle
17	chr11:101319600-101320200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:101319600-101324200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr11:101319800-101321000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:101320000-101336600	Weak transcription	Ovary	ovary
21	chr11:101320800-101321000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr11:101321200-101328600	Weak transcription	NHDF-Ad	bronchial
23	chr11:101322000-101324800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr11:101324000-101324400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr11:101324000-101324600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:101324000-101324800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:101324200-101324600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr11:101324200-101324800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr11:101324200-101324800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:101324200-101325000	Enhancers	Osteobl	bone
31	chr11:101324400-101324800	Enhancers	NH-A	brain
32	chr11:101324400-101325000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:101324600-101326000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:101324800-101327800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:101324800-101328600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr11:101325000-101328000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:101325000-101329000	Weak transcription	NHLF	lung
38	chr11:101325000-101329000	Weak transcription	Osteobl	bone
39	chr11:101326000-101326200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:101326200-101326400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:101327800-101328400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:101327800-101328400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr11:101327800-101329600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:101328000-101329400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:101328400-101329800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:101328400-101329800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr11:101328600-101329400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:101328600-101329400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr11:101328600-101329600	Enhancers	NHDF-Ad	bronchial
50	chr11:101328800-101329200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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