Variant report

Variant	nsv522241
Chromosome Location	chr8:119995697-120027871
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	BHLHE40	chr8:120009066-120009211	GM12878	blood:	n/a	n/a
2	CEBPB	chr8:120013623-120013823	HepG2	liver:	n/a	chr8:120013752-120013763
3	CEBPB	chr8:120017222-120017539	HepG2	liver:	n/a	chr8:120017383-120017392 chr8:120017381-120017392 chr8:120017381-120017394 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017381-120017394 chr8:120017383-120017394
4	CEBPB	chr8:120027031-120027342	HepG2	liver:	n/a	chr8:120027187-120027198
5	CEBPB	chr8:120017236-120017505	Hela-S3	cervix:	n/a	chr8:120017383-120017392 chr8:120017381-120017392 chr8:120017381-120017394 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017381-120017394 chr8:120017383-120017394
6	CEBPB	chr8:120017230-120017563	IMR90	lung:	n/a	chr8:120017383-120017392 chr8:120017381-120017392 chr8:120017381-120017394 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017381-120017394 chr8:120017383-120017394
7	CEBPB	chr8:120018351-120018592	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:120017219-120017554	A549	lung:	n/a	chr8:120017383-120017392 chr8:120017381-120017392 chr8:120017381-120017394 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017381-120017394 chr8:120017383-120017394
9	CEBPB	chr8:120013579-120013931	Hela-S3	cervix:	n/a	chr8:120013752-120013763
10	CEBPB	chr8:120017350-120017401	H1-hESC	embryonic stem cell:	n/a	chr8:120017383-120017392 chr8:120017381-120017392 chr8:120017381-120017394 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017383-120017392 chr8:120017381-120017394 chr8:120017383-120017394
11	CEBPB	chr8:120013588-120013932	IMR90	lung:	n/a	chr8:120013752-120013763
12	CEBPB	chr8:120013675-120013902	H1-hESC	embryonic stem cell:	n/a	chr8:120013752-120013763
13	CEBPB	chr8:119999041-119999359	HepG2	liver:	n/a	chr8:119999207-119999218
14	CEBPB	chr8:120027086-120027358	A549	lung:	n/a	chr8:120027187-120027198
15	CEBPB	chr8:120007423-120007848	IMR90	lung:	n/a	n/a
16	CTCF	chr8:120018040-120018190	GM12865	blood:	n/a	n/a
17	CTCF	chr8:120017960-120018110	HMEC	breast:	n/a	n/a
18	CTCF	chr8:120018160-120018310	AG04449	skin:	n/a	n/a
19	CTCF	chr8:120018120-120018270	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr8:120018114-120018243	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr8:120018120-120018270	HRE	kidney:	n/a	n/a
22	CTCF	chr8:120018060-120018210	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:120018080-120018230	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:120018060-120018210	AG09319	gingival:	n/a	n/a
25	CTCF	chr8:120018380-120018530	AG04450	lung:	n/a	n/a
26	CTCF	chr8:120018100-120018250	HAc	cerebellar:	n/a	n/a
27	CTCF	chr8:120018120-120018270	Caco-2	colon:	n/a	n/a
28	CTCF	chr8:120018080-120018230	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:120018180-120018330	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr8:120018060-120018210	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr8:120018120-120018270	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr8:120018100-120018250	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr8:120018120-120018270	HPF	lung:	n/a	n/a
34	CTCF	chr8:120018120-120018270	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr8:120018080-120018230	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr8:120018080-120018230	NHEK	skin:	n/a	n/a
37	CTCF	chr8:120018100-120018250	NHLF	lung:	n/a	n/a
38	CTCF	chr8:120018120-120018270	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr8:120018080-120018230	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr8:120018100-120018250	HMF	breast:	n/a	n/a
41	CTCF	chr8:120018100-120018250	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr8:120017940-120018090	HVMF	connective:	n/a	n/a
43	CTCF	chr8:120018140-120018290	HCM	heart:	n/a	n/a
44	CTCF	chr8:120018120-120018270	HEK293	kidney:	n/a	n/a
45	CTCF	chr8:120018080-120018230	AG09319	gingival:	n/a	n/a
46	CTCF	chr8:120018140-120018290	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr8:120018080-120018230	HFF	foreskin:	n/a	n/a
48	CTCF	chr8:120018120-120018270	HMF	breast:	n/a	n/a
49	CTCF	chr8:119999593-119999693	LNCaP	prostate:	n/a	n/a
50	CTCF	chr8:120018040-120018190	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:120007022-120007072	HNPCEpiC	eye:	n/a
2	chr8:120007022-120007072	HepG2	liver:	n/a
3	chr8:120007022-120007072	HUVEC	blood vessel:	n/a
4	chr8:120007022-120007072	SAEC	small airway:	n/a
5	chr8:120007022-120007072	BE2_C	brain:	n/a
6	chr8:120007022-120007072	NHDF-neo	bronchial:	n/a
7	chr8:120007022-120007072	Caco-2	colon:	n/a
8	chr8:120007022-120007072	AG04449	skin:	fetal
9	chr8:120007022-120007072	NH-A	brain:	n/a
10	chr8:120007022-120007072	AG09319	gingival:	n/a
11	chr8:120007022-120007072	AG10803	skin:	n/a
12	chr8:120007022-120007072	GM19239	blood:	n/a
13	chr8:120007022-120007072	Jurkat	blood:	n/a
14	chr8:120007022-120007072	GM06990	blood:	n/a
15	chr8:120007022-120007072	HCPEpiC	choroid plexus:	n/a
16	chr8:120007022-120007072	NHBE	bronchial:	n/a
17	chr8:120007022-120007072	A549	lung:	n/a
18	chr8:120007022-120007072	GM12891	blood:	n/a
19	chr8:120007022-120007072	HRPEpiC	eye:	n/a
20	chr8:120007022-120007072	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:120007022-120007072	HRE	kidney:	n/a
22	chr8:120007022-120007072	CMK	blood:	n/a
23	chr8:120007022-120007072	U87	brain:	n/a
24	chr8:120007022-120007072	AG09309	skin:	n/a
25	chr8:120007022-120007072	HCM	heart:	n/a
26	chr8:120007022-120007072	H1-hESC	embryonic stem cell:	embryo
27	chr8:120007022-120007072	MCF10A-Er-Src	breast:	n/a
28	chr8:120007022-120007072	PrEC	prostate:	n/a
29	chr8:120007022-120007072	T-47D	breast:	n/a
30	chr8:120007022-120007072	LNCaP	prostate:	n/a
31	chr8:120007022-120007072	SK-N-MC	brain:	n/a
32	chr8:120007022-120007072	SKMC	muscle:	n/a
33	chr8:120007022-120007072	HCT-116	colon:	n/a
34	chr8:120007022-120007072	HCF	heart:	n/a
35	chr8:120007022-120007072	AG04450	lung:	fetal
36	chr8:120007022-120007072	K562	blood:	n/a
37	chr8:120007022-120007072	PANC-1	pancreas:	n/a
38	chr8:120007022-120007072	HEEpiC	esophagus:	n/a
39	chr8:120007022-120007072	NT2-D1	testis:	n/a
40	chr8:120007022-120007072	SK-N-SH	brain:	n/a
41	chr8:120007022-120007072	GM12892	blood:	n/a
42	chr8:120007022-120007072	ovcar-3	ovarian:	n/a
43	chr8:120007022-120007072	HEK293	kidney:	embryo
44	chr8:120007022-120007072	AoSMC	blood vessel:	n/a
45	chr8:120007022-120007072	HIPEpiC	eye:	n/a
46	chr8:120007022-120007072	Hela-S3	cervix:	n/a
47	chr8:120007022-120007072	Hepatocyte	liver:	n/a
48	chr8:120007022-120007072	ECC-1	luminal epithelium:	n/a
49	chr8:120007022-120007072	IMR90	lung:	fetal
50	chr8:120007022-120007072	PFSK-1	brain:	n/a

Variant related genes	Relation type
COLEC10	TF binding region
ENSG00000254247	TF binding region
COLEC10	CpG island
ENSG00000254247	CpG island

Extended variants
information (count: 917 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9942821	chr8:119995697-119995698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117812806	chr8:119995728-119995729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527581562	chr8:119995743-119995744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569398421	chr8:119995760-119995761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549254220	chr8:119995768-119995769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114506400	chr8:119995774-119995775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73709511	chr8:119995778-119995779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549733918	chr8:119995788-119995789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191833241	chr8:119995825-119995826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539584809	chr8:119995843-119995844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs80287157	chr8:119995851-119995852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572852894	chr8:119995891-119995892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149690367	chr8:119995905-119995906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555604388	chr8:119995915-119995916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574013951	chr8:119995943-119995944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369994672	chr8:119995992-119995993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368170787	chr8:119996033-119996034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562974670	chr8:119996051-119996052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112712784	chr8:119996054-119996055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145538039	chr8:119996080-119996081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560294339	chr8:119996189-119996190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115062234	chr8:119996194-119996195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373994200	chr8:119996207-119996208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148818488	chr8:119996239-119996240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561140070	chr8:119996267-119996268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531538703	chr8:119996274-119996275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143453177	chr8:119996366-119996367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141778459	chr8:119996393-119996394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185006432	chr8:119996418-119996419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543908920	chr8:119996452-119996453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35621247	chr8:119996467-119996468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533466011	chr8:119996488-119996489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146509190	chr8:119996492-119996493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566638146	chr8:119996500-119996501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562293544	chr8:119996529-119996530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375331508	chr8:119996530-119996531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567756068	chr8:119996546-119996547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529832830	chr8:119996569-119996570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548402156	chr8:119996595-119996596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74812665	chr8:119996619-119996620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117283098	chr8:119996620-119996621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538195025	chr8:119996674-119996675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7826524	chr8:119996675-119996676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs578076318	chr8:119996701-119996702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141116830	chr8:119996769-119996770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77702838	chr8:119996787-119996788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76911225	chr8:119996817-119996818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80344349	chr8:119996836-119996837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560903989	chr8:119996847-119996848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111344780	chr8:119996868-119996869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119992800-120000600	Weak transcription	NHDF-Ad	bronchial
2	chr8:119995400-120001600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:120000600-120001000	Enhancers	NHDF-Ad	bronchial
4	chr8:120000600-120001200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:120000600-120001200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:120000600-120001200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr8:120000600-120001200	Enhancers	Hela-S3	cervix
8	chr8:120001000-120001600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:120006400-120008400	Enhancers	Fetal Heart	heart
10	chr8:120006800-120007000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:120006800-120007000	Enhancers	Right Ventricle	heart
12	chr8:120006800-120007400	Enhancers	HSMMtube	muscle
13	chr8:120006800-120008000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:120006800-120008200	Enhancers	Osteobl	bone
15	chr8:120007000-120007800	Weak transcription	Right Ventricle	heart
16	chr8:120007000-120013600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:120007200-120008000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:120007200-120008000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:120007200-120008000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr8:120007200-120008000	Enhancers	NHLF	lung
21	chr8:120007200-120008400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:120007200-120008400	Enhancers	NH-A	brain
23	chr8:120007400-120007600	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr8:120007800-120008000	Enhancers	Aorta	Aorta
25	chr8:120007800-120008400	Enhancers	Right Ventricle	heart
26	chr8:120008000-120012400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:120008400-120009600	Weak transcription	Right Ventricle	heart
28	chr8:120008400-120012000	Weak transcription	Fetal Heart	heart
29	chr8:120009800-120010000	Enhancers	Right Ventricle	heart
30	chr8:120012000-120013000	Enhancers	Fetal Heart	heart
31	chr8:120012400-120012800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:120012800-120018000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:120013400-120014000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:120013600-120013800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:120018000-120019600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:120019600-120021000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:120021000-120021200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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