Variant report

Variant	nsv1029401
Chromosome Location	chr8:79366260-79427487
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	chr8:79419872-79420116	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:79420431-79420703	HepG2	liver:	n/a	n/a
3	ATF2	chr8:79423002-79423385	GM12878	blood:	n/a	n/a
4	BATF	chr8:79422965-79423234	GM12878	blood:	n/a	n/a
5	BATF	chr8:79422932-79423247	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:79400379-79400575	HepG2	liver:	n/a	chr8:79400507-79400518
7	CEBPB	chr8:79383826-79384099	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:79422855-79423169	A549	lung:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
9	CEBPB	chr8:79369507-79369707	A549	lung:	n/a	n/a
10	CEBPB	chr8:79383005-79383219	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:79422795-79423264	MCF-7	breast:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
12	CEBPB	chr8:79422829-79423174	Hela-S3	cervix:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
13	CEBPB	chr8:79382933-79383110	MCF-7	breast:	n/a	n/a
14	CEBPB	chr8:79422849-79423199	HepG2	liver:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
15	CEBPB	chr8:79393442-79393551	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:79422797-79423160	MCF-7	breast:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
17	CEBPB	chr8:79422835-79423187	IMR90	lung:	n/a	chr8:79423015-79423026 chr8:79423017-79423026 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423015-79423028 chr8:79423015-79423028 chr8:79423017-79423026 chr8:79423017-79423028
18	CHD1	chr8:79427306-79430000	IMR90	lung:	n/a	chr8:79428495-79428505 chr8:79428613-79428623
19	CTCF	chr8:79419860-79420010	K562	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
20	CTCF	chr8:79419860-79420010	A549	lung:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
21	CTCF	chr8:79419814-79420095	Spleen_OC	spleen:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
22	CTCF	chr8:79419800-79419950	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr8:79419880-79420030	HPAF	blood vessel:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
24	CTCF	chr8:79419820-79419970	GM12875	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967
25	CTCF	chr8:79419708-79420746	SK-N-SH	brain:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
26	CTCF	chr8:79419860-79420010	RPTEC	kidney:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
27	CTCF	chr8:79419880-79420030	GM12875	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
28	CTCF	chr8:79419900-79420050	GM12878	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
29	CTCF	chr8:79419800-79419950	HVMF	connective:	n/a	n/a
30	CTCF	chr8:79419900-79420050	GM12871	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
31	CTCF	chr8:79419900-79420050	HPF	lung:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
32	CTCF	chr8:79419900-79420050	GM12864	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
33	CTCF	chr8:79419860-79420038	GM13976	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
34	CTCF	chr8:79419616-79420366	HCT-116	colon:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
35	CTCF	chr8:79419781-79420123	SK-N-SH_RA	brain:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
36	CTCF	chr8:79419880-79420030	BE2_C	brain:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
37	CTCF	chr8:79402040-79402190	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:79419900-79420050	HCFaa	heart:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
39	CTCF	chr8:79419900-79420050	HRE	kidney:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
40	CTCF	chr8:79419882-79420059	HepG2	liver:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
41	CTCF	chr8:79419900-79420050	HCT-116	colon:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
42	CTCF	chr8:79419900-79420050	BJ	skin:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
43	CTCF	chr8:79419900-79420050	NHDF-neo	bronchial:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
44	CTCF	chr8:79419860-79420010	SAEC	small airway:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
45	CTCF	chr8:79419751-79420275	MCF-7	breast:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
46	CTCF	chr8:79419839-79420085	GM13977	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
47	CTCF	chr8:79419860-79420010	GM12869	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
48	CTCF	chr8:79419900-79420050	HCM	heart:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
49	CTCF	chr8:79419840-79419990	HA-sp	spinal cord:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973
50	CTCF	chr8:79419880-79420030	GM12864	blood:	n/a	chr8:79419950-79419968 chr8:79419951-79419967 chr8:79419952-79419973

No.	Distal block	Cell Line	Cell type
1	chr8:79410893..79411697-chr8:79419823..79420388,2	K562	blood:
2	chr8:79420413..79426569-chr8:79426863..79431107,5	MCF-7	breast:
3	chr8:79419499..79420416-chr8:79442084..79442972,6	MCF-7	breast:
4	chr8:79423918..79426841-chr8:79427285..79430314,3	MCF-7	breast:
5	chr8:79420915..79422835-chr8:79428460..79430735,2	MCF-7	breast:
6	chr8:79419518..79421514-chr8:79518015..79520151,2	MCF-7	breast:
7	chr8:79420594..79422389-chr8:79424976..79426839,2	MCF-7	breast:
8	chr8:79423442..79426104-chr8:79439954..79442867,2	MCF-7	breast:
9	chr8:79419743..79422501-chr8:79439751..79442069,2	MCF-7	breast:
10	chr8:79419533..79420037-chr8:79764408..79765064,2	MCF-7	breast:
11	chr22:39640025..39642519-chr8:79419690..79422250,2	MCF-7	breast:
12	chr8:79418638..79421599-chr8:79440731..79442586,3	MCF-7	breast:
13	chr20:56283155..56284954-chr8:79396075..79397773,2	MCF-7	breast:
14	chr8:79410893..79411697-chr8:79419823..79420388,2	K562	blood:
15	chr8:79419378..79420481-chr8:79527083..79528366,7	MCF-7	breast:
16	chr8:79419785..79420445-chr8:79527063..79528030,4	MCF-7	breast:
17	chr8:79419078..79420072-chr8:79441781..79442729,2	MCF-7	breast:
18	chr8:79420594..79422389-chr8:79424976..79426839,2	MCF-7	breast:
19	chr8:79402266..79404340-chr8:79413420..79415402,2	MCF-7	breast:
20	chr8:79402266..79404340-chr8:79413420..79415402,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL7-1	chr8:79392489-79392570	ENSG00000254266

Variant related genes	Relation type
PKIA	TF binding region
ENSG00000100311	chromatin interactions
ENSG00000171033	chromatin interactions
ENSG00000260398	chromatin interactions
ENSG00000124225	chromatin interactions

Extended variants
information (count: 828 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188056221	chr8:79373621-79373622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547064675	chr8:79373666-79373667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114591452	chr8:79373678-79373679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144175281	chr8:79373698-79373699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115493757	chr8:79373701-79373702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568982931	chr8:79373747-79373748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74448130	chr8:79373827-79373828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9298313	chr8:79373850-79373851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576932747	chr8:79373874-79373875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533824819	chr8:79373896-79373897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558138128	chr8:79373904-79373905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570067219	chr8:79373920-79373921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537571759	chr8:79373929-79373930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201578196	chr8:79373938-79373939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547684189	chr8:79373939-79373940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192685353	chr8:79373959-79373960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559370485	chr8:79373976-79373977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543234053	chr8:79373999-79374000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148687184	chr8:79374017-79374018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573522526	chr8:79374053-79374054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184928802	chr8:79374090-79374091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530919329	chr8:79374098-79374099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567523769	chr8:79374102-79374103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536652791	chr8:79374124-79374125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544599500	chr8:79374166-79374167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563025126	chr8:79374174-79374175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188765832	chr8:79374178-79374179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548414225	chr8:79374186-79374187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181614844	chr8:79374193-79374194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10216378	chr8:79374229-79374230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552019100	chr8:79374278-79374279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs118166158	chr8:79374288-79374289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200892548	chr8:79374312-79374313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537476785	chr8:79374325-79374326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555869888	chr8:79374327-79374328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368520726	chr8:79374360-79374361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs36123114	chr8:79374366-79374367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35636730	chr8:79374367-79374368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531105183	chr8:79374373-79374374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373291568	chr8:79374377-79374378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535195112	chr8:79374386-79374387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184565009	chr8:79374426-79374427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573314647	chr8:79374433-79374434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540941026	chr8:79374518-79374519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559263762	chr8:79374553-79374554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4072526	chr8:79374556-79374557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142188727	chr8:79374595-79374596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562738354	chr8:79374607-79374608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189253087	chr8:79374632-79374633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530216286	chr8:79374633-79374634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Colorectal cancer	19455253	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	21251322	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:79373600-79374400	Enhancers	H9 Cell Line	embryonic stem cell
2	chr8:79374400-79378200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:79377800-79378000	ZNF genes & repeats	Esophagus	oesophagus
4	chr8:79378200-79378600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:79383400-79383800	Enhancers	Placenta	Placenta
6	chr8:79394600-79396800	Enhancers	Placenta	Placenta
7	chr8:79396400-79396600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr8:79396800-79397200	Weak transcription	Placenta	Placenta
9	chr8:79397200-79397400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr8:79397200-79398600	Enhancers	Placenta	Placenta
11	chr8:79397600-79398600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:79397600-79398600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:79397800-79398200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:79398000-79398400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:79405800-79408200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:79407200-79408200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:79407400-79407600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:79407400-79407600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:79407400-79408000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:79407400-79408200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:79407400-79408200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr8:79407600-79409000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:79407600-79410200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:79408000-79409200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:79408200-79408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:79408200-79408800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:79408200-79409000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr8:79408600-79409400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr8:79408600-79409600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:79408800-79409200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:79408800-79409800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr8:79408800-79410200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:79409000-79410000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:79409000-79410000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr8:79409200-79409800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:79409400-79409600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr8:79409600-79409800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:79409800-79410000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr8:79410000-79410400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:79410800-79411800	Enhancers	Liver	Liver
41	chr8:79419600-79420000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr8:79419800-79420000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:79419800-79420000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr8:79419800-79420800	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr8:79419800-79421000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:79419800-79421800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr8:79420000-79420200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:79420000-79420200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr8:79420000-79420200	Enhancers	HUVEC	blood vessel
50	chr8:79420000-79420200	Flanking Active TSS	Osteobl	bone

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