Variant report

Variant	nsv1047030
Chromosome Location	chr11:84067493-84187274
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	ATF2	chr11:84101419-84101830	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:84141751-84142100	H1-hESC	embryonic stem cell:	n/a	chr11:84141926-84141940
3	BACH1	chr11:84140016-84140019	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr11:84136756-84137055	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr11:84151167-84151180	A549	lung:	n/a	n/a
6	CEBPB	chr11:84183894-84184118	A549	lung:	n/a	chr11:84184028-84184039
7	CEBPB	chr11:84183871-84184127	HepG2	liver:	n/a	chr11:84184028-84184039
8	CEBPB	chr11:84122660-84122850	A549	lung:	n/a	chr11:84122781-84122792
9	CEBPB	chr11:84182615-84182815	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:84171267-84171571	HepG2	liver:	n/a	chr11:84171410-84171421
11	CEBPB	chr11:84100957-84101265	HepG2	liver:	n/a	chr11:84101113-84101126 chr11:84101115-84101126 chr11:84101113-84101124
12	CEBPB	chr11:84100948-84101275	IMR90	lung:	n/a	chr11:84101113-84101126 chr11:84101115-84101126 chr11:84101113-84101124
13	CEBPB	chr11:84086013-84086082	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:84134517-84134717	HepG2	liver:	n/a	chr11:84134593-84134604
15	CEBPB	chr11:84130464-84130473	K562	blood:	n/a	n/a
16	CEBPB	chr11:84122683-84122913	HepG2	liver:	n/a	chr11:84122781-84122792
17	CEBPB	chr11:84171302-84171535	A549	lung:	n/a	chr11:84171410-84171421
18	CEBPB	chr11:84100940-84101223	A549	lung:	n/a	chr11:84101113-84101126 chr11:84101115-84101126 chr11:84101113-84101124
19	CEBPB	chr11:84122606-84122937	IMR90	lung:	n/a	chr11:84122781-84122792
20	CEBPB	chr11:84100964-84101171	H1-hESC	embryonic stem cell:	n/a	chr11:84101113-84101126 chr11:84101115-84101126 chr11:84101113-84101124
21	CEBPB	chr11:84125990-84126278	H1-hESC	embryonic stem cell:	n/a	chr11:84126120-84126133 chr11:84126120-84126133 chr11:84126120-84126131 chr11:84126119-84126136
22	CHD2	chr11:84069135-84069188	GM12878	blood:	n/a	n/a
23	CHD2	chr11:84148510-84148763	GM12878	blood:	n/a	n/a
24	CTCF	chr11:84095780-84095930	Hela-S3	cervix:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
25	CTCF	chr11:84101600-84101750	GM12873	blood:	n/a	n/a
26	CTCF	chr11:84109118-84109406	A549	lung:	n/a	n/a
27	CTCF	chr11:84095460-84095610	AG04449	skin:	n/a	n/a
28	CTCF	chr11:84109160-84109310	HFF	foreskin:	n/a	n/a
29	CTCF	chr11:84148640-84148790	SAEC	small airway:	n/a	n/a
30	CTCF	chr11:84095770-84095955	A549	lung:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
31	CTCF	chr11:84095820-84095970	HRE	kidney:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
32	CTCF	chr11:84095748-84096075	MCF-7	breast:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
33	CTCF	chr11:84095820-84095970	Caco-2	colon:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
34	CTCF	chr11:84095754-84095983	Kidney_OC	kidney:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
35	CTCF	chr11:84095780-84095930	HCT-116	colon:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
36	CTCF	chr11:84109200-84109350	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr11:84095760-84095910	GM12873	blood:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
38	CTCF	chr11:84109167-84109364	HepG2	liver:	n/a	n/a
39	CTCF	chr11:84095780-84095930	GM12872	blood:	n/a	chr11:84095868-84095881 chr11:84095867-84095888 chr11:84095865-84095883 chr11:84095866-84095882
40	CTCF	chr11:84109460-84109610	GM12866	blood:	n/a	n/a
41	CTCF	chr11:84148660-84148810	HMEC	breast:	n/a	n/a
42	CTCF	chr11:84095480-84095630	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr11:84148680-84148830	GM12867	blood:	n/a	n/a
44	CTCF	chr11:84109180-84109330	SAEC	small airway:	n/a	n/a
45	CTCF	chr11:84109220-84109370	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr11:84096500-84096650	AG10803	skin:	n/a	n/a
47	CTCF	chr11:84101480-84101630	BE2_C	brain:	n/a	n/a
48	CTCF	chr11:84101409-84101895	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:84095700-84095850	HAc	cerebellar:	n/a	n/a
50	CTCF	chr11:84148620-84148770	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:84148821-84148871	ProgFib	skin:	n/a
2	chr11:84148821-84148871	NHBE	bronchial:	n/a
3	chr11:84148821-84148871	RPTEC	kidney:	n/a
4	chr11:84148821-84148871	HCF	heart:	n/a
5	chr11:84148821-84148871	A549	lung:	n/a
6	chr11:84148821-84148871	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:84148821-84148871	HIPEpiC	eye:	n/a
8	chr11:84148821-84148871	T-47D	breast:	n/a
9	chr11:84148821-84148871	ECC-1	luminal epithelium:	n/a
10	chr11:84148821-84148871	HRE	kidney:	n/a
11	chr11:84148821-84148871	HCT-116	colon:	n/a
12	chr11:84148821-84148871	GM06990	blood:	n/a
13	chr11:84148821-84148871	NHDF-neo	bronchial:	n/a
14	chr11:84148821-84148871	BJ	skin:	n/a
15	chr11:84148821-84148871	NH-A	brain:	n/a
16	chr11:84148821-84148871	HRCEpiC	kidney:	n/a
17	chr11:84148821-84148871	GM12878	blood:	n/a
18	chr11:84148821-84148871	HAEpiC	amniotic membrane:	n/a
19	chr11:84148821-84148871	HMEC	breast:	n/a
20	chr11:84148821-84148871	NT2-D1	testis:	n/a
21	chr11:84148821-84148871	HL-60	blood:	n/a
22	chr11:84148821-84148871	Hela-S3	cervix:	n/a
23	chr11:84148821-84148871	LNCaP	prostate:	n/a
24	chr11:84148821-84148871	SAEC	small airway:	n/a
25	chr11:84148821-84148871	BE2_C	brain:	n/a
26	chr11:84148821-84148871	HepG2	liver:	n/a
27	chr11:84148821-84148871	PrEC	prostate:	n/a
28	chr11:84148821-84148871	HUVEC	blood vessel:	n/a
29	chr11:84148821-84148871	AG04449	skin:	fetal
30	chr11:84148821-84148871	ovcar-3	ovarian:	n/a
31	chr11:84148821-84148871	Hepatocyte	liver:	n/a
32	chr11:84148821-84148871	H1-hESC	embryonic stem cell:	embryo
33	chr11:84148821-84148871	SK-N-MC	brain:	n/a
34	chr11:84148821-84148871	SK-N-SH_RA	brain:	n/a
35	chr11:84148821-84148871	AG09319	gingival:	n/a
36	chr11:84148821-84148871	MCF-7	breast:	n/a
37	chr11:84148821-84148871	HEEpiC	esophagus:	n/a
38	chr11:84148821-84148871	HCM	heart:	n/a
39	chr11:84148821-84148871	U87	brain:	n/a
40	chr11:84148821-84148871	AG09309	skin:	n/a
41	chr11:84148821-84148871	AoSMC	blood vessel:	n/a
42	chr11:84148821-84148871	CMK	blood:	n/a
43	chr11:84148821-84148871	GM19239	blood:	n/a
44	chr11:84148821-84148871	GM12891	blood:	n/a
45	chr11:84148821-84148871	MCF10A-Er-Src	breast:	n/a
46	chr11:84148821-84148871	SK-N-SH	brain:	n/a
47	chr11:84148821-84148871	K562	blood:	n/a
48	chr11:84148821-84148871	HCPEpiC	choroid plexus:	n/a
49	chr11:84148821-84148871	HEK293	kidney:	embryo
50	chr11:84148821-84148871	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:84101555..84102182-chr11:84275381..84276078,3	MCF-7	breast:
2	chr11:84176346..84177970-chr11:84178773..84180913,2	K562	blood:
3	chr11:84101210..84102180-chr11:84235286..84236202,6	MCF-7	breast:
4	chr11:83547847..83548466-chr11:84095653..84096338,3	MCF-7	breast:
5	chr11:84089926..84090860-chr12:115240902..115241508,2	MCF-7	breast:
6	chr11:84176346..84177970-chr11:84178773..84180913,2	K562	blood:
7	chr11:84108756..84109961-chr11:84235215..84236409,11	MCF-7	breast:
8	chr11:84101140..84101859-chr11:84425077..84425854,3	MCF-7	breast:
9	chr11:84108744..84109714-chr11:84235378..84236188,5	MCF-7	breast:
10	chr11:83666922..83667791-chr11:84095425..84096103,2	MCF-7	breast:
11	chr11:83547273..83548254-chr11:84095723..84096301,2	MCF-7	breast:
12	chr11:84108848..84109482-chr11:84236612..84237134,2	MCF-7	breast:
13	chr10:104033091..104033703-chr11:84109108..84109675,2	MCF-7	breast:
14	chr11:84095332..84096338-chr11:84235259..84236211,4	MCF-7	breast:

Variant related genes	Relation type
DLG2	TF binding region
DLG2	CpG island

Extended variants
information (count: 3710 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3710 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143068703	chr11:84067543-84067544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370449879	chr11:84067672-84067673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182045791	chr11:84067751-84067752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556988193	chr11:84067774-84067775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186519045	chr11:84067779-84067780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544536276	chr11:84067784-84067785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539297135	chr11:84067799-84067800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189049132	chr11:84067813-84067814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576951415	chr11:84067821-84067822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181724051	chr11:84067854-84067855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138688261	chr11:84067887-84067888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373573687	chr11:84067906-84067907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574746885	chr11:84067910-84067911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556471423	chr11:84067948-84067949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542160101	chr11:84067949-84067950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564017233	chr11:84067965-84067966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185535262	chr11:84067988-84067989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6592177	chr11:84067997-84067998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs564649010	chr11:84068002-84068003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528658047	chr11:84068025-84068026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546393497	chr11:84068050-84068051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568110699	chr11:84068063-84068064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528887176	chr11:84068088-84068089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191190630	chr11:84068120-84068121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568854480	chr11:84068149-84068150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557075110	chr11:84068186-84068187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539325524	chr11:84068191-84068192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557601890	chr11:84068207-84068208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566343231	chr11:84068244-84068245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142707825	chr11:84068258-84068259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147345679	chr11:84068259-84068260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6592178	chr11:84068261-84068262	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7928075	chr11:84068267-84068268	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557375741	chr11:84068268-84068269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139773451	chr11:84068271-84068272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141780369	chr11:84068283-84068284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564736106	chr11:84068305-84068306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150574226	chr11:84068341-84068342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560285959	chr11:84068391-84068392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540777811	chr11:84068408-84068409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561682218	chr11:84068492-84068493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528975950	chr11:84068496-84068497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74862296	chr11:84068502-84068503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528625448	chr11:84068514-84068515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3914464	chr11:84068534-84068535	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572610265	chr11:84068549-84068550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180758882	chr11:84068658-84068659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561953269	chr11:84068661-84068662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551268972	chr11:84068676-84068677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541319952	chr11:84068697-84068698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	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
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Cancer	20164920	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ductal carcinoma	22052326	CNVD
Autism	19246517	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84067000-84067600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr11:84067000-84067600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr11:84067200-84067600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr11:84067400-84067600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:84067600-84071600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:84068000-84068200	Enhancers	Brain Hippocampus Middle	brain
7	chr11:84068200-84068800	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr11:84068800-84069400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr11:84069400-84069600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr11:84069800-84071000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:84071000-84071400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:84071600-84071800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:84072000-84072400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:84078200-84078800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr11:84078200-84079000	Enhancers	Brain Substantia Nigra	brain
16	chr11:84078200-84079200	Enhancers	Brain Cingulate Gyrus	brain
17	chr11:84078400-84078800	Enhancers	Brain Angular Gyrus	brain
18	chr11:84083200-84083600	Enhancers	Brain Germinal Matrix	brain
19	chr11:84089200-84089400	Enhancers	Brain Cingulate Gyrus	brain
20	chr11:84089400-84092800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:84092600-84092800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:84092800-84093200	Enhancers	Brain Hippocampus Middle	brain
23	chr11:84092800-84093600	Enhancers	Brain Cingulate Gyrus	brain
24	chr11:84093200-84096000	Weak transcription	Brain Hippocampus Middle	brain
25	chr11:84093600-84094000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr11:84094000-84094200	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:84094200-84101000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr11:84094600-84095000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:84094800-84095000	Enhancers	Fetal Brain Male	brain
30	chr11:84095000-84095600	Enhancers	Brain Substantia Nigra	brain
31	chr11:84095200-84096000	Weak transcription	Fetal Brain Male	brain
32	chr11:84096000-84096400	Enhancers	Brain Hippocampus Middle	brain
33	chr11:84096000-84097000	Enhancers	Fetal Brain Male	brain
34	chr11:84101000-84101200	Enhancers	Brain Cingulate Gyrus	brain
35	chr11:84101000-84101400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:84101200-84101600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:84101200-84102000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr11:84101200-84102000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr11:84101200-84102200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:84101400-84102000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr11:84101400-84102000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:84101400-84102000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr11:84101400-84102200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:84101600-84102000	Enhancers	Brain Cingulate Gyrus	brain
45	chr11:84102000-84105800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr11:84102200-84107600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr11:84105800-84108000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr11:84107400-84108200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:84107400-84109000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:84107400-84109200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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