Variant report

Variant	nsv933973
Chromosome Location	chr7:147438206-147549993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:289)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:147528563-147528613	K562	blood:	n/a	n/a
2	CCNT2	chr7:147506163-147506338	K562	blood:	n/a	n/a
3	CCNT2	chr7:147489824-147489960	K562	blood:	n/a	n/a
4	CEBPB	chr7:147489290-147489429	K562	blood:	n/a	n/a
5	CEBPB	chr7:147463487-147463559	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:147510157-147510402	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:147456805-147457007	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:147465939-147466112	K562	blood:	n/a	chr7:147465965-147465976
9	CTCF	chr7:147471660-147471810	BE2_C	brain:	n/a	n/a
10	CTCF	chr7:147528380-147528530	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:147486660-147486810	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr7:147486700-147486850	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr7:147486727-147486869	Fibrobl	skin:	n/a	n/a
14	CTCF	chr7:147486741-147486852	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:147503380-147503530	HCFaa	heart:	n/a	n/a
16	CTCF	chr7:147539260-147539410	GM12864	blood:	n/a	n/a
17	CTCF	chr7:147503380-147503530	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:147503400-147503550	HPF	lung:	n/a	n/a
19	CTCF	chr7:147486660-147486810	BE2_C	brain:	n/a	n/a
20	CTCF	chr7:147503340-147503490	RPTEC	kidney:	n/a	n/a
21	CTCF	chr7:147503360-147503510	Caco-2	colon:	n/a	n/a
22	CTCF	chr7:147486708-147486867	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:147532880-147533030	AG09309	skin:	n/a	n/a
24	CTCF	chr7:147486691-147486891	GM12878	blood:	n/a	n/a
25	CTCF	chr7:147486680-147486830	AG10803	skin:	n/a	n/a
26	CTCF	chr7:147486753-147486840	A549	lung:	n/a	n/a
27	CTCF	chr7:147503400-147503550	BJ	skin:	n/a	n/a
28	CTCF	chr7:147528579-147528619	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:147486660-147486810	AG04449	skin:	n/a	n/a
30	CTCF	chr7:147503400-147503550	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr7:147493760-147493910	GM12871	blood:	n/a	n/a
32	CTCF	chr7:147503500-147503650	AG04450	lung:	n/a	n/a
33	CTCF	chr7:147486744-147486857	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:147486666-147486856	Medullo	brain:	n/a	n/a
35	CTCF	chr7:147439840-147439990	AG10803	skin:	n/a	n/a
36	CTCF	chr7:147503380-147503530	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr7:147471720-147471870	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:147486736-147486844	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:147503300-147503450	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:147486726-147486849	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:147486739-147486840	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:147486704-147486857	ProgFib	skin:	n/a	n/a
43	CTCF	chr7:147524360-147524510	HVMF	connective:	n/a	n/a
44	CTCF	chr7:147528525-147528627	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:147486684-147486827	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr7:147503360-147503510	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:147486680-147486830	NB4	blood:	n/a	n/a
48	CTCF	chr7:147503420-147503570	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr7:147503400-147503550	AG10803	skin:	n/a	n/a
50	CTCF	chr7:147486723-147486863	LNCaP	prostate:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:147500503-147500553	AG04449	skin:	fetal
2	chr7:147500722-147500772	AG04449	skin:	fetal
3	chr7:147500503-147500553	PANC-1	pancreas:	n/a
4	chr7:147500722-147500772	LNCaP	prostate:	n/a
5	chr7:147500722-147500772	MCF10A-Er-Src	breast:	n/a
6	chr7:147500503-147500553	GM12892	blood:	n/a
7	chr7:147500503-147500553	U87	brain:	n/a
8	chr7:147500503-147500553	SKMC	muscle:	n/a
9	chr7:147500722-147500772	ECC-1	luminal epithelium:	n/a
10	chr7:147500503-147500553	AG10803	skin:	n/a
11	chr7:147500503-147500553	ovcar-3	ovarian:	n/a
12	chr7:147500722-147500772	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:147500722-147500772	HRCEpiC	kidney:	n/a
14	chr7:147500722-147500772	HEEpiC	esophagus:	n/a
15	chr7:147500722-147500772	AG09319	gingival:	n/a
16	chr7:147500503-147500553	HNPCEpiC	eye:	n/a
17	chr7:147500503-147500553	HCM	heart:	n/a
18	chr7:147500722-147500772	HMEC	breast:	n/a
19	chr7:147500503-147500553	SK-N-SH	brain:	n/a
20	chr7:147500503-147500553	HRE	kidney:	n/a
21	chr7:147500722-147500772	HEK293	kidney:	embryo
22	chr7:147500503-147500553	HCF	heart:	n/a
23	chr7:147500503-147500553	HL-60	blood:	n/a
24	chr7:147500503-147500553	RPTEC	kidney:	n/a
25	chr7:147500722-147500772	AG04450	lung:	fetal
26	chr7:147500722-147500772	NH-A	brain:	n/a
27	chr7:147500722-147500772	PANC-1	pancreas:	n/a
28	chr7:147500722-147500772	HCM	heart:	n/a
29	chr7:147500722-147500772	HRPEpiC	eye:	n/a
30	chr7:147500503-147500553	Jurkat	blood:	n/a
31	chr7:147500722-147500772	MCF-7	breast:	n/a
32	chr7:147500503-147500553	HAEpiC	amniotic membrane:	n/a
33	chr7:147500722-147500772	GM12891	blood:	n/a
34	chr7:147500503-147500553	A549	lung:	n/a
35	chr7:147500503-147500553	HEK293	kidney:	embryo
36	chr7:147500722-147500772	NT2-D1	testis:	n/a
37	chr7:147500503-147500553	Hela-S3	cervix:	n/a
38	chr7:147500503-147500553	ProgFib	skin:	n/a
39	chr7:147500503-147500553	SAEC	small airway:	n/a
40	chr7:147500722-147500772	HUVEC	blood vessel:	n/a
41	chr7:147500722-147500772	IMR90	lung:	fetal
42	chr7:147500722-147500772	GM06990	blood:	n/a
43	chr7:147500503-147500553	NHBE	bronchial:	n/a
44	chr7:147500503-147500553	SK-N-MC	brain:	n/a
45	chr7:147500722-147500772	HAEpiC	amniotic membrane:	n/a
46	chr7:147500503-147500553	PrEC	prostate:	n/a
47	chr7:147500722-147500772	CMK	blood:	n/a
48	chr7:147500722-147500772	HIPEpiC	eye:	n/a
49	chr7:147500722-147500772	HCPEpiC	choroid plexus:	n/a
50	chr7:147500503-147500553	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:39750814..39753511-chr7:147523706..147526586,2	MCF-7	breast:
2	chr17:57920819..57922347-chr7:147503999..147506112,2	MCF-7	breast:
3	chr3:105481713..105484437-chr7:147483253..147485905,2	MCF-7	breast:
4	chr7:147545107..147547622-chr7:147549641..147552092,2	K562	blood:
5	chr7:147446008..147448178-chr7:147448478..147451242,2	K562	blood:
6	chr7:147468495..147470634-chr7:147474029..147476158,2	K562	blood:
7	chr3:4392578..4393170-chr7:147445471..147445972,2	K562	blood:
8	chr7:147446008..147448178-chr7:147448478..147451242,2	K562	blood:
9	chr7:147468495..147470634-chr7:147474029..147476158,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP249	TF binding region
RNU6-1184P	TF binding region
RNA5SP249	CpG island
RNU6-1184P	CpG island
ENSG00000264020	chromatin interactions
ENSG00000251936	chromatin interactions

Extended variants
information (count: 2567 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2567 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76546829	chr7:147438313-147438314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115076211	chr7:147438358-147438359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555538958	chr7:147438404-147438405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78057814	chr7:147438435-147438436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17417028	chr7:147438445-147438446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553708869	chr7:147438449-147438450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371219954	chr7:147438456-147438457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75275713	chr7:147438464-147438465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577535123	chr7:147438468-147438469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543376481	chr7:147438525-147438526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571983390	chr7:147438527-147438528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573512910	chr7:147438582-147438583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542405940	chr7:147438583-147438584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375920707	chr7:147438607-147438608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139970583	chr7:147438639-147438640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6953679	chr7:147438666-147438667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs116726722	chr7:147438683-147438684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12703966	chr7:147438708-147438709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2177722	chr7:147438726-147438727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs74616546	chr7:147438736-147438737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547303918	chr7:147438802-147438803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113023480	chr7:147438808-147438809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138758504	chr7:147438816-147438817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202201388	chr7:147438823-147438824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530362301	chr7:147438825-147438826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547191524	chr7:147438829-147438830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565811866	chr7:147438906-147438907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35809968	chr7:147438908-147438909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534438396	chr7:147438932-147438933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551431701	chr7:147438942-147438943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191651332	chr7:147438989-147438990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537011051	chr7:147438990-147438991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200633425	chr7:147439034-147439035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34565048	chr7:147439036-147439037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557015217	chr7:147439071-147439072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542302896	chr7:147439090-147439091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558448380	chr7:147439101-147439102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113356902	chr7:147439123-147439124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376736094	chr7:147439136-147439137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536071028	chr7:147439173-147439174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542897844	chr7:147439174-147439175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182238292	chr7:147439175-147439176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371234130	chr7:147439179-147439180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545174143	chr7:147439193-147439194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573320282	chr7:147439223-147439224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112179998	chr7:147439224-147439225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555143271	chr7:147439225-147439226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111715768	chr7:147439271-147439272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544589102	chr7:147439290-147439291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76489104	chr7:147439322-147439323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147437800-147439200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:147439200-147440800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:147439600-147440000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:147440800-147441000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:147450200-147451000	Enhancers	Brain Hippocampus Middle	brain
6	chr7:147451000-147452800	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:147451800-147453600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:147452800-147454200	Enhancers	Brain Hippocampus Middle	brain
9	chr7:147453200-147453400	Enhancers	Brain Anterior Caudate	brain
10	chr7:147453400-147453800	Enhancers	Brain Substantia Nigra	brain
11	chr7:147453400-147454200	Enhancers	Fetal Lung	lung
12	chr7:147453600-147454800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:147453800-147458600	Weak transcription	Brain Substantia Nigra	brain
14	chr7:147453800-147460600	Weak transcription	Brain Angular Gyrus	brain
15	chr7:147454200-147454400	Enhancers	Brain Anterior Caudate	brain
16	chr7:147454200-147456400	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:147454800-147455600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:147456200-147457600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:147456400-147456800	Enhancers	Brain Hippocampus Middle	brain
20	chr7:147456800-147458800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:147456800-147459200	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:147458600-147459200	Enhancers	Brain Substantia Nigra	brain
23	chr7:147458800-147459000	Enhancers	Brain Cingulate Gyrus	brain
24	chr7:147459000-147460600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr7:147459200-147460600	Weak transcription	Brain Substantia Nigra	brain
26	chr7:147459200-147461200	Enhancers	Brain Hippocampus Middle	brain
27	chr7:147460600-147461200	Enhancers	Brain Angular Gyrus	brain
28	chr7:147460600-147461200	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:147460600-147461200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr7:147460600-147461600	Enhancers	Brain Substantia Nigra	brain
31	chr7:147461200-147464600	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:147461200-147469600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr7:147461200-147472800	Weak transcription	Brain Angular Gyrus	brain
34	chr7:147461600-147466600	Weak transcription	Brain Substantia Nigra	brain
35	chr7:147464600-147465600	Enhancers	Brain Hippocampus Middle	brain
36	chr7:147465600-147465800	Weak transcription	Brain Hippocampus Middle	brain
37	chr7:147465800-147466800	Enhancers	Brain Hippocampus Middle	brain
38	chr7:147466600-147468600	Enhancers	Brain Substantia Nigra	brain
39	chr7:147466800-147469800	Weak transcription	Brain Hippocampus Middle	brain
40	chr7:147468200-147468600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr7:147468200-147468800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:147468200-147468800	Active TSS	Brain Anterior Caudate	brain
43	chr7:147468200-147468800	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr7:147468200-147469000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:147468400-147468800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:147468400-147469000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:147468600-147469800	Weak transcription	Brain Substantia Nigra	brain
48	chr7:147468800-147469400	Enhancers	Brain Anterior Caudate	brain
49	chr7:147468800-147472600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:147468800-147472600	Weak transcription	Brain Inferior Temporal Lobe	brain

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