Variant report

Variant	nsv415
Chromosome Location	chr11:83924941-83969603
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	chr11:83955584-83955943	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:83961981-83962644	HepG2	liver:	n/a	n/a
3	ATF2	chr11:83960704-83961065	GM12878	blood:	n/a	n/a
4	ATF2	chr11:83954542-83955275	GM12878	blood:	n/a	n/a
5	ATF2	chr11:83954620-83955077	GM12878	blood:	n/a	n/a
6	BACH1	chr11:83966610-83966776	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:83954647-83955262	GM12878	blood:	n/a	n/a
8	BATF	chr11:83967709-83967966	GM12878	blood:	n/a	chr11:83967769-83967778
9	BATF	chr11:83967677-83967977	GM12878	blood:	n/a	chr11:83967769-83967778
10	BATF	chr11:83954638-83954970	GM12878	blood:	n/a	n/a
11	BATF	chr11:83960789-83961066	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:83954618-83954994	GM12878	blood:	n/a	n/a
13	BCL3	chr11:83954621-83955187	GM12878	blood:	n/a	n/a
14	BCLAF1	chr11:83954585-83955005	GM12878	blood:	n/a	n/a
15	CEBPB	chr11:83955462-83955718	HepG2	liver:	n/a	chr11:83955655-83955666 chr11:83955641-83955652 chr11:83955643-83955654
16	CEBPB	chr11:83958874-83959155	A549	lung:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
17	CEBPB	chr11:83955491-83955695	HepG2	liver:	n/a	chr11:83955655-83955666 chr11:83955641-83955652 chr11:83955643-83955654
18	CEBPB	chr11:83957186-83957370	HepG2	liver:	n/a	chr11:83957305-83957316
19	CEBPB	chr11:83958879-83959076	Hela-S3	cervix:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
20	CEBPB	chr11:83954646-83955190	GM12878	blood:	n/a	n/a
21	CEBPB	chr11:83957265-83957447	A549	lung:	n/a	chr11:83957305-83957316
22	CEBPB	chr11:83955497-83955825	MCF-7	breast:	n/a	chr11:83955655-83955666 chr11:83955641-83955652 chr11:83955643-83955654
23	CEBPB	chr11:83939029-83939276	Hela-S3	cervix:	n/a	chr11:83939239-83939251 chr11:83939142-83939155
24	CEBPB	chr11:83938994-83939287	IMR90	lung:	n/a	chr11:83939239-83939251 chr11:83939142-83939155
25	CEBPB	chr11:83955538-83955883	MCF-7	breast:	n/a	chr11:83955655-83955666 chr11:83955641-83955652 chr11:83955643-83955654
26	CEBPB	chr11:83958837-83959190	HepG2	liver:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
27	CEBPB	chr11:83958854-83959192	IMR90	lung:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
28	CEBPB	chr11:83957160-83957473	Hela-S3	cervix:	n/a	chr11:83957305-83957316
29	CEBPB	chr11:83935162-83935326	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:83955464-83955835	HepG2	liver:	n/a	chr11:83955655-83955666 chr11:83955641-83955652 chr11:83955643-83955654
31	CEBPB	chr11:83958868-83959150	H1-hESC	embryonic stem cell:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
32	CEBPB	chr11:83958806-83959208	MCF-7	breast:	n/a	chr11:83959002-83959011 chr11:83959000-83959013 chr11:83959002-83959011 chr11:83959002-83959011
33	CTCF	chr11:83960900-83961050	GM12864	blood:	n/a	n/a
34	CTCF	chr11:83960982-83961076	GM13977	blood:	n/a	n/a
35	CTCF	chr11:83960980-83961130	GM12873	blood:	n/a	n/a
36	CTCF	chr11:83960980-83961130	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr11:83960992-83961076	GM12891	blood:	n/a	n/a
38	CTCF	chr11:83961000-83961150	GM12878	blood:	n/a	n/a
39	CTCF	chr11:83960880-83961030	SAEC	small airway:	n/a	n/a
40	CTCF	chr11:83960940-83961090	RPTEC	kidney:	n/a	n/a
41	CTCF	chr11:83960957-83961074	GM12878	blood:	n/a	n/a
42	CTCF	chr11:83960820-83960970	NHEK	skin:	n/a	n/a
43	CTCF	chr11:83960900-83961050	GM12871	blood:	n/a	n/a
44	CTCF	chr11:83961000-83961150	GM12864	blood:	n/a	n/a
45	CTCF	chr11:83960920-83961070	GM12865	blood:	n/a	n/a
46	CTCF	chr11:83960985-83961069	GM10248	blood:	n/a	n/a
47	CTCF	chr11:83960920-83961070	GM12864	blood:	n/a	n/a
48	CTCF	chr11:83961000-83961063	GM19238	blood:	n/a	n/a
49	CTCF	chr11:83960983-83961080	GM12892	blood:	n/a	n/a
50	CTCF	chr11:83961074-83961083	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:83952986-83953036	NHDF-neo	bronchial:	n/a
2	chr11:83952986-83953036	NT2-D1	testis:	n/a
3	chr11:83952986-83953036	NH-A	brain:	n/a
4	chr11:83952986-83953036	SK-N-MC	brain:	n/a
5	chr11:83952986-83953036	NB4	blood:	n/a
6	chr11:83952986-83953036	HRE	kidney:	n/a
7	chr11:83952986-83953036	HEEpiC	esophagus:	n/a
8	chr11:83952986-83953036	HAEpiC	amniotic membrane:	n/a
9	chr11:83952986-83953036	ProgFib	skin:	n/a
10	chr11:83952986-83953036	ovcar-3	ovarian:	n/a
11	chr11:83952986-83953036	AG04449	skin:	fetal
12	chr11:83952986-83953036	AoSMC	blood vessel:	n/a
13	chr11:83952986-83953036	Jurkat	blood:	n/a
14	chr11:83952986-83953036	HUVEC	blood vessel:	n/a
15	chr11:83952986-83953036	HNPCEpiC	eye:	n/a
16	chr11:83952986-83953036	PrEC	prostate:	n/a
17	chr11:83952986-83953036	LNCaP	prostate:	n/a
18	chr11:83952986-83953036	HRCEpiC	kidney:	n/a
19	chr11:83952986-83953036	HIPEpiC	eye:	n/a
20	chr11:83952986-83953036	ECC-1	luminal epithelium:	n/a
21	chr11:83952986-83953036	MCF10A-Er-Src	breast:	n/a
22	chr11:83952986-83953036	AG10803	skin:	n/a
23	chr11:83952986-83953036	H1-hESC	embryonic stem cell:	embryo
24	chr11:83952986-83953036	A549	lung:	n/a
25	chr11:83952986-83953036	T-47D	breast:	n/a
26	chr11:83952986-83953036	SAEC	small airway:	n/a
27	chr11:83952986-83953036	GM12892	blood:	n/a
28	chr11:83952986-83953036	HRPEpiC	eye:	n/a
29	chr11:83952986-83953036	Caco-2	colon:	n/a
30	chr11:83952986-83953036	RPTEC	kidney:	n/a
31	chr11:83952986-83953036	AG09309	skin:	n/a
32	chr11:83952986-83953036	HL-60	blood:	n/a
33	chr11:83952986-83953036	GM12891	blood:	n/a
34	chr11:83952986-83953036	MCF-7	breast:	n/a
35	chr11:83952986-83953036	BE2_C	brain:	n/a
36	chr11:83952986-83953036	HEK293	kidney:	embryo
37	chr11:83952986-83953036	IMR90	lung:	fetal
38	chr11:83952986-83953036	AG04450	lung:	fetal
39	chr11:83952986-83953036	U87	brain:	n/a
40	chr11:83952986-83953036	Hela-S3	cervix:	n/a
41	chr11:83952986-83953036	SK-N-SH	brain:	n/a
42	chr11:83952986-83953036	GM06990	blood:	n/a
43	chr11:83952986-83953036	AG09319	gingival:	n/a
44	chr11:83952986-83953036	HepG2	liver:	n/a
45	chr11:83952986-83953036	Hepatocyte	liver:	n/a
46	chr11:83952986-83953036	GM19239	blood:	n/a
47	chr11:83952986-83953036	HCM	heart:	n/a
48	chr11:83952986-83953036	SK-N-SH_RA	brain:	n/a
49	chr11:83952986-83953036	PANC-1	pancreas:	n/a
50	chr11:83952986-83953036	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:83951528..83953158-chr11:83957231..83960545,3	MCF-7	breast:
2	chr11:83932523..83935495-chr11:83937155..83939564,2	MCF-7	breast:
3	chr11:83932523..83935495-chr11:83937155..83939564,2	MCF-7	breast:
4	chr11:83967920..83969714-chr11:83971819..83973395,2	K562	blood:
5	chr11:83919298..83920953-chr11:83927515..83929488,2	K562	blood:
6	chr11:83921898..83923535-chr11:83927297..83928996,2	MCF-7	breast:
7	chr11:83951528..83953158-chr11:83957231..83960545,3	MCF-7	breast:
8	chr11:83941713..83944829-chr11:83950244..83953336,4	MCF-7	breast:
9	chr11:83966425..83969420-chr11:83971895..83974336,2	K562	blood:
10	chr11:83941713..83944829-chr11:83950244..83953336,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264838	TF binding region
ENSG00000264838	CpG island

Extended variants
information (count: 1628 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182150710	chr11:83924952-83924953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186715757	chr11:83925134-83925135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569954667	chr11:83925164-83925165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190793659	chr11:83925173-83925174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183910080	chr11:83925180-83925181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576841895	chr11:83925194-83925195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563191905	chr11:83925206-83925207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576769298	chr11:83925237-83925238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369809281	chr11:83925238-83925239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202021284	chr11:83925265-83925266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552965299	chr11:83925271-83925272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111588728	chr11:83925287-83925288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7120366	chr11:83925293-83925294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542189175	chr11:83925297-83925298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200249136	chr11:83925305-83925306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113709685	chr11:83925317-83925318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530089530	chr11:83925326-83925327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532422807	chr11:83925327-83925328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575516571	chr11:83925363-83925364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188509836	chr11:83925378-83925379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146026904	chr11:83925388-83925389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71468370	chr11:83925435-83925436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs547552275	chr11:83925469-83925470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116925302	chr11:83925487-83925488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571469512	chr11:83925507-83925508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192892133	chr11:83925512-83925513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139942207	chr11:83925546-83925547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143355243	chr11:83925622-83925623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79188469	chr11:83925643-83925644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144305080	chr11:83925776-83925777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570939507	chr11:83925808-83925809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534741448	chr11:83925852-83925853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12786897	chr11:83925901-83925902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574497274	chr11:83925935-83925936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535395939	chr11:83925968-83925969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115944724	chr11:83926020-83926021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557316551	chr11:83926024-83926025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115336767	chr11:83926032-83926033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545765709	chr11:83926054-83926055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564334502	chr11:83926065-83926066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572950395	chr11:83926127-83926128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11233951	chr11:83926211-83926212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559548342	chr11:83926218-83926219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530038753	chr11:83926220-83926221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531334773	chr11:83926273-83926274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548148873	chr11:83926297-83926298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563652393	chr11:83926306-83926307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531141961	chr11:83926387-83926388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552570246	chr11:83926394-83926395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547558338	chr11:83926448-83926449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83924200-83926400	Weak transcription	Brain Substantia Nigra	brain
2	chr11:83924200-83935000	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:83926600-83927200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:83929000-83929800	Enhancers	Aorta	Aorta
5	chr11:83929400-83929800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:83929400-83929800	Active TSS	Right Atrium	heart
7	chr11:83929600-83930000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr11:83929600-83930200	Enhancers	Fetal Heart	heart
9	chr11:83929600-83930400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:83929800-83930800	Weak transcription	Aorta	Aorta
11	chr11:83930800-83931000	Enhancers	Aorta	Aorta
12	chr11:83934800-83936800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr11:83935000-83935200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr11:83935000-83936600	Enhancers	Brain Cingulate Gyrus	brain
15	chr11:83935000-83936600	Enhancers	Brain Hippocampus Middle	brain
16	chr11:83935000-83937200	Enhancers	Brain Angular Gyrus	brain
17	chr11:83935000-83937600	Enhancers	Brain Substantia Nigra	brain
18	chr11:83935200-83935400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr11:83935200-83945400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:83935400-83944600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:83935800-83936600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:83936000-83936600	Enhancers	Brain Anterior Caudate	brain
23	chr11:83936000-83937600	Enhancers	Liver	Liver
24	chr11:83936600-83939000	Weak transcription	Brain Hippocampus Middle	brain
25	chr11:83936600-83939600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:83936600-83939800	Weak transcription	Brain Anterior Caudate	brain
27	chr11:83936600-83942400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr11:83936800-83939200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr11:83937200-83939200	Weak transcription	Brain Angular Gyrus	brain
30	chr11:83937600-83939200	Weak transcription	Liver	Liver
31	chr11:83937600-83939200	Weak transcription	Brain Substantia Nigra	brain
32	chr11:83939000-83940000	Enhancers	Brain Hippocampus Middle	brain
33	chr11:83939200-83939400	Enhancers	Liver	Liver
34	chr11:83939200-83939600	Enhancers	Brain Germinal Matrix	brain
35	chr11:83939200-83940000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr11:83939200-83940000	Enhancers	Brain Substantia Nigra	brain
37	chr11:83939200-83940800	Enhancers	Brain Angular Gyrus	brain
38	chr11:83939600-83940000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:83939600-83945200	Weak transcription	Brain Germinal Matrix	brain
40	chr11:83939800-83940000	Enhancers	Brain Anterior Caudate	brain
41	chr11:83940000-83940400	Weak transcription	Brain Anterior Caudate	brain
42	chr11:83940000-83941000	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:83940000-83943600	Weak transcription	Brain Substantia Nigra	brain
44	chr11:83940000-83944000	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr11:83940000-83945000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:83940400-83940600	Enhancers	Brain Anterior Caudate	brain
47	chr11:83940600-83944200	Weak transcription	Brain Anterior Caudate	brain
48	chr11:83940800-83945000	Weak transcription	Brain Angular Gyrus	brain
49	chr11:83941000-83946200	Enhancers	Brain Hippocampus Middle	brain
50	chr11:83942400-83943400	Enhancers	Brain Cingulate Gyrus	brain

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