Variant report

Variant	nsv465375
Chromosome Location	chr8:4201459-4251284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:72)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:72 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:4242430-4242568	A549	lung:	n/a	n/a
2	CEBPB	chr8:4227126-4227302	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:4250895-4251106	HepG2	liver:	n/a	chr8:4250917-4250928
4	CEBPB	chr8:4214721-4214989	HepG2	liver:	n/a	chr8:4214850-4214859 chr8:4214850-4214859 chr8:4214850-4214859
5	CEBPB	chr8:4227032-4227320	HepG2	liver:	n/a	n/a
6	CTCF	chr8:4210730-4210766	Lung_OC	lung:	n/a	n/a
7	CTCF	chr8:4220060-4220210	HRE	kidney:	n/a	n/a
8	CTCF	chr8:4219946-4220263	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:4220100-4220250	HL-60	blood:	n/a	n/a
10	CTCF	chr8:4220120-4220270	HMF	breast:	n/a	n/a
11	CTCF	chr8:4220076-4220209	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr8:4210715-4210728	Lung_OC	lung:	n/a	n/a
13	CTCF	chr8:4220100-4220250	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr8:4220160-4220310	HRE	kidney:	n/a	n/a
15	CTCF	chr8:4220147-4220189	HepG2	liver:	n/a	n/a
16	CTCF	chr8:4220160-4220310	HCFaa	heart:	n/a	n/a
17	CTCF	chr8:4228467-4228491	GM13976	blood:	n/a	n/a
18	CTCF	chr8:4244652-4244790	Pancreas_OC	pancreas:	n/a	chr8:4244685-4244706 chr8:4244691-4244707 chr8:4244690-4244708
19	CTCF	chr8:4220120-4220270	HMEC	breast:	n/a	n/a
20	E2F4	chr8:4226844-4226993	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr8:4204744-4204868	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F6	chr8:4238516-4239067	H1-hESC	embryonic stem cell:	n/a	chr8:4238782-4238793 chr8:4238779-4238796 chr8:4238779-4238796
23	E2F6	chr8:4238700-4238954	H1-hESC	embryonic stem cell:	n/a	chr8:4238782-4238793 chr8:4238779-4238796 chr8:4238779-4238796
24	IRF3	chr8:4216325-4216449	GM12878	blood:	n/a	n/a
25	JUND	chr8:4238746-4238897	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAFF	chr8:4236818-4237053	K562	blood:	n/a	chr8:4236963-4236981
27	MAFF	chr8:4208326-4208608	HepG2	liver:	n/a	n/a
28	MAFF	chr8:4236803-4237153	HepG2	liver:	n/a	chr8:4236963-4236981
29	MAFF	chr8:4215565-4215857	HepG2	liver:	n/a	n/a
30	MAFK	chr8:4236804-4237130	HepG2	liver:	n/a	n/a
31	MAFK	chr8:4215520-4215848	HepG2	liver:	n/a	n/a
32	MAFK	chr8:4236798-4237141	IMR90	lung:	n/a	n/a
33	MAFK	chr8:4236799-4237157	HepG2	liver:	n/a	n/a
34	MAFK	chr8:4236834-4237070	K562	blood:	n/a	n/a
35	MAFK	chr8:4208307-4208603	HepG2	liver:	n/a	n/a
36	MAFK	chr8:4215557-4215845	HepG2	liver:	n/a	n/a
37	MAFK	chr8:4208315-4208602	HepG2	liver:	n/a	n/a
38	MAX	chr8:4223695-4223982	NB4	blood:	n/a	chr8:4223873-4223883
39	MAX	chr8:4238698-4238996	H1-hESC	embryonic stem cell:	n/a	n/a
40	MYC	chr8:4229982-4230032	K562	blood:	n/a	n/a
41	MYC	chr8:4208130-4208166	NB4	blood:	n/a	n/a
42	NRF1	chr8:4226012-4226023	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr8:4203186-4203627	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr8:4229569-4229769	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr8:4201439-4202036	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr8:4236535-4236729	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr8:4220394-4220514	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr8:4214725-4214925	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr8:4248044-4248184	GM12878	blood:	n/a	n/a
50	POLR2A	chr8:4224060-4224107	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4238976-4239026	PrEC	prostate:	n/a
2	chr8:4238976-4239026	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:4238976-4239026	BJ	skin:	n/a
4	chr8:4238976-4239026	A549	lung:	n/a
5	chr8:4238976-4239026	NHBE	bronchial:	n/a
6	chr8:4238976-4239026	NB4	blood:	n/a
7	chr8:4238976-4239026	AG04449	skin:	fetal
8	chr8:4238976-4239026	HCPEpiC	choroid plexus:	n/a
9	chr8:4238976-4239026	SKMC	muscle:	n/a
10	chr8:4238976-4239026	HEK293	kidney:	embryo
11	chr8:4238976-4239026	GM12878	blood:	n/a
12	chr8:4238976-4239026	PFSK-1	brain:	n/a
13	chr8:4238976-4239026	AG09309	skin:	n/a
14	chr8:4238976-4239026	SK-N-MC	brain:	n/a
15	chr8:4238976-4239026	GM12892	blood:	n/a
16	chr8:4238976-4239026	ovcar-3	ovarian:	n/a
17	chr8:4238976-4239026	NH-A	brain:	n/a
18	chr8:4238976-4239026	AG10803	skin:	n/a
19	chr8:4238976-4239026	ECC-1	luminal epithelium:	n/a
20	chr8:4238976-4239026	IMR90	lung:	fetal
21	chr8:4238976-4239026	HRCEpiC	kidney:	n/a
22	chr8:4238976-4239026	AG09319	gingival:	n/a
23	chr8:4238976-4239026	SK-N-SH	brain:	n/a
24	chr8:4238976-4239026	Caco-2	colon:	n/a
25	chr8:4238976-4239026	HCM	heart:	n/a
26	chr8:4238976-4239026	HCF	heart:	n/a
27	chr8:4238976-4239026	SAEC	small airway:	n/a
28	chr8:4238976-4239026	HL-60	blood:	n/a
29	chr8:4238976-4239026	LNCaP	prostate:	n/a
30	chr8:4238976-4239026	HAEpiC	amniotic membrane:	n/a
31	chr8:4238976-4239026	HNPCEpiC	eye:	n/a
32	chr8:4238976-4239026	NT2-D1	testis:	n/a
33	chr8:4238976-4239026	BE2_C	brain:	n/a
34	chr8:4238976-4239026	PANC-1	pancreas:	n/a
35	chr8:4238976-4239026	ProgFib	skin:	n/a
36	chr8:4238976-4239026	HMEC	breast:	n/a
37	chr8:4238976-4239026	GM06990	blood:	n/a
38	chr8:4238976-4239026	MCF-7	breast:	n/a
39	chr8:4238976-4239026	AG04450	lung:	fetal
40	chr8:4238976-4239026	HUVEC	blood vessel:	n/a
41	chr8:4238976-4239026	SK-N-SH_RA	brain:	n/a
42	chr8:4238976-4239026	HEEpiC	esophagus:	n/a
43	chr8:4238976-4239026	Hela-S3	cervix:	n/a
44	chr8:4238976-4239026	HIPEpiC	eye:	n/a
45	chr8:4238976-4239026	Jurkat	blood:	n/a
46	chr8:4238976-4239026	CMK	blood:	n/a
47	chr8:4238976-4239026	HRPEpiC	eye:	n/a
48	chr8:4238976-4239026	HCT-116	colon:	n/a
49	chr8:4238976-4239026	GM12891	blood:	n/a
50	chr8:4238976-4239026	Hepatocyte	liver:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-8	chr8:4250344-4250612	NONHSAT124750

No data

Variant related genes	Relation type
RN7SL872P	TF binding region
RN7SL872P	CpG island

Extended variants
information (count: 1660 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11984458	chr8:4201459-4201460	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568217327	chr8:4201465-4201466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144808585	chr8:4201469-4201470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112440221	chr8:4201478-4201479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184118946	chr8:4201485-4201486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543391501	chr8:4201487-4201488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543655115	chr8:4201499-4201500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188466473	chr8:4201554-4201555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573847434	chr8:4201558-4201559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541263716	chr8:4201562-4201563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537512505	chr8:4201577-4201578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181020688	chr8:4201583-4201584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141316573	chr8:4201589-4201590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150801190	chr8:4201594-4201595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184314947	chr8:4201607-4201608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545792257	chr8:4201608-4201609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs137858284	chr8:4201623-4201624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528638850	chr8:4201632-4201633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73174297	chr8:4201652-4201653	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113177288	chr8:4201668-4201669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190672897	chr8:4201675-4201676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553735809	chr8:4201684-4201685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573564961	chr8:4201691-4201692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572399133	chr8:4201694-4201695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550799769	chr8:4201696-4201697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149470497	chr8:4201710-4201711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536267735	chr8:4201716-4201717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181926767	chr8:4201719-4201720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561543779	chr8:4201727-4201728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77974528	chr8:4201737-4201738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78040969	chr8:4201743-4201744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553247045	chr8:4201752-4201753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577773045	chr8:4201753-4201754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545058415	chr8:4201764-4201765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187051073	chr8:4201780-4201781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561081075	chr8:4201782-4201783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs80100036	chr8:4201794-4201795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs17069980	chr8:4201796-4201797	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190496974	chr8:4201798-4201799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116400894	chr8:4201799-4201800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373095669	chr8:4201805-4201806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376652219	chr8:4201809-4201810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532619328	chr8:4201836-4201837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551019817	chr8:4201837-4201838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569287874	chr8:4201840-4201841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371511828	chr8:4201847-4201848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549935349	chr8:4201857-4201858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147161857	chr8:4201873-4201874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548652244	chr8:4201879-4201880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531970167	chr8:4201890-4201891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Schizophrenia	21346763	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4194200-4202600	Weak transcription	Pancreas	Pancrea
2	chr8:4194800-4202600	Weak transcription	Gastric	stomach
3	chr8:4199200-4201800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:4200800-4201600	Weak transcription	Stomach Mucosa	stomach
5	chr8:4201600-4203000	Enhancers	Stomach Mucosa	stomach
6	chr8:4201800-4203200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:4202600-4202800	Enhancers	Gastric	stomach
8	chr8:4202600-4202800	Enhancers	Pancreas	Pancrea
9	chr8:4203400-4203600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:4213200-4216000	Weak transcription	Fetal Intestine Small	intestine
11	chr8:4215400-4216000	Enhancers	Fetal Intestine Large	intestine
12	chr8:4215800-4216200	Enhancers	Fetal Muscle Leg	muscle
13	chr8:4216000-4216600	Enhancers	Duodenum Mucosa	Duodenum
14	chr8:4216000-4217000	Weak transcription	Fetal Intestine Large	intestine
15	chr8:4216000-4217600	Enhancers	Fetal Intestine Small	intestine
16	chr8:4216200-4217200	Weak transcription	Fetal Muscle Leg	muscle
17	chr8:4216600-4217600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:4217000-4217600	Enhancers	Fetal Intestine Large	intestine
19	chr8:4217200-4217400	Enhancers	Fetal Muscle Leg	muscle
20	chr8:4217600-4217800	Enhancers	Duodenum Mucosa	Duodenum
21	chr8:4221400-4224800	Enhancers	Dnd41	blood
22	chr8:4223000-4223800	Enhancers	Fetal Thymus	thymus
23	chr8:4229200-4229800	Enhancers	Liver	Liver
24	chr8:4232800-4233000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:4233000-4233800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:4235800-4236000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:4236000-4236200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:4236200-4238800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:4238800-4239200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:4238800-4239200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:4238800-4239400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:4238800-4239400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:4238800-4239400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:4239000-4239200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:4239000-4240000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr8:4240400-4240600	Enhancers	Psoas Muscle	Psoas

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