Variant report

Variant	nsv610931
Chromosome Location	chr8:34176474-34226215
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	BACH1	chr8:34184100-34184468	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr8:34210214-34210414	K562	blood:	n/a	n/a
3	CEBPB	chr8:34186498-34186701	H1-hESC	embryonic stem cell:	n/a	chr8:34186572-34186583 chr8:34186573-34186584 chr8:34186574-34186583
4	CEBPB	chr8:34186188-34186692	IMR90	lung:	n/a	chr8:34186311-34186324 chr8:34186572-34186583 chr8:34186573-34186584 chr8:34186574-34186583
5	CEBPB	chr8:34180719-34180937	A549	lung:	n/a	chr8:34180830-34180841
6	CEBPB	chr8:34186193-34186726	HepG2	liver:	n/a	chr8:34186311-34186324 chr8:34186572-34186583 chr8:34186573-34186584 chr8:34186574-34186583
7	CEBPB	chr8:34186281-34186727	A549	lung:	n/a	chr8:34186311-34186324 chr8:34186572-34186583 chr8:34186573-34186584 chr8:34186574-34186583
8	CEBPB	chr8:34180694-34180980	HepG2	liver:	n/a	chr8:34180830-34180841
9	CTCF	chr8:34192807-34193018	Medullo	brain:	n/a	chr8:34192912-34192930
10	CTCF	chr8:34193460-34193610	HRPEpiC	eye:	n/a	chr8:34193570-34193579
11	CTCF	chr8:34192800-34192950	HRE	kidney:	n/a	chr8:34192912-34192930
12	CTCF	chr8:34193459-34193666	Medullo	brain:	n/a	chr8:34193570-34193579
13	CTCF	chr8:34193533-34193595	H1-hESC	embryonic stem cell:	n/a	chr8:34193570-34193579
14	CTCF	chr8:34193500-34193650	GM12868	blood:	n/a	chr8:34193570-34193579
15	CTCF	chr8:34193460-34193610	WERI-Rb-1	eye:	n/a	chr8:34193570-34193579
16	CTCF	chr8:34192820-34192970	WERI-Rb-1	eye:	n/a	chr8:34192912-34192930
17	CTCF	chr8:34193500-34193650	WERI-Rb-1	eye:	n/a	chr8:34193570-34193579
18	E2F4	chr8:34222578-34223022	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr8:34203939-34204193	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr8:34203950-34204259	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr8:34203958-34204282	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr8:34215726-34215799	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr8:34205522-34205606	HUVEC	blood vessel:	n/a	n/a
24	FOS	chr8:34215676-34215799	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:34215747-34215951	MCF10A-Er-Src	breast:	n/a	n/a
26	FOXA1	chr8:34206667-34206888	T-47D	breast:	n/a	n/a
27	FOXA1	chr8:34206620-34206848	T-47D	breast:	n/a	n/a
28	JUN	chr8:34208977-34209481	K562	blood:	n/a	chr8:34209299-34209308
29	JUND	chr8:34179919-34180126	HepG2	liver:	n/a	chr8:34179999-34180008 chr8:34180054-34180065 chr8:34180054-34180066 chr8:34180056-34180064 chr8:34180057-34180064 chr8:34180056-34180065 chr8:34180055-34180064 chr8:34180052-34180063
30	JUND	chr8:34217745-34217908	HepG2	liver:	n/a	chr8:34217795-34217806
31	KAP1	chr8:34223066-34223504	K562	blood:	n/a	n/a
32	MAFF	chr8:34184087-34184348	HepG2	liver:	n/a	chr8:34184231-34184249
33	MAFK	chr8:34184047-34184575	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAFK	chr8:34184110-34184363	HepG2	liver:	n/a	n/a
35	MAX	chr8:34193375-34193660	H1-hESC	embryonic stem cell:	n/a	chr8:34193560-34193576
36	MAZ	chr8:34200619-34200737	HepG2	liver:	n/a	n/a
37	MYC	chr8:34203984-34204288	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr8:34178898-34178937	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr8:34192667-34192859	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr8:34180426-34180669	GM12878	blood:	n/a	n/a
41	POLR2A	chr8:34193708-34193869	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr8:34220232-34220399	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr8:34197218-34197251	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr8:34218064-34218239	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr8:34210209-34210240	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr8:34202187-34202386	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr8:34217853-34217979	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr8:34207360-34207623	MCF10A-Er-Src	breast:	n/a	n/a
49	RAD21	chr8:34182340-34182666	H1-hESC	embryonic stem cell:	n/a	n/a
50	RAD21	chr8:34193365-34193754	H1-hESC	embryonic stem cell:	n/a	chr8:34193572-34193581

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:34182528-34182578	Caco-2	colon:	n/a
2	chr8:34182528-34182578	HCM	heart:	n/a
3	chr8:34182528-34182578	PFSK-1	brain:	n/a
4	chr8:34182528-34182578	PrEC	prostate:	n/a
5	chr8:34182528-34182578	SK-N-MC	brain:	n/a
6	chr8:34182528-34182578	HRE	kidney:	n/a
7	chr8:34182528-34182578	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:34182528-34182578	MCF-7	breast:	n/a
9	chr8:34182528-34182578	RPTEC	kidney:	n/a
10	chr8:34182528-34182578	HNPCEpiC	eye:	n/a
11	chr8:34182528-34182578	NHBE	bronchial:	n/a
12	chr8:34182528-34182578	HRPEpiC	eye:	n/a
13	chr8:34182528-34182578	GM19239	blood:	n/a
14	chr8:34182528-34182578	HL-60	blood:	n/a
15	chr8:34182528-34182578	NB4	blood:	n/a
16	chr8:34182528-34182578	HAEpiC	amniotic membrane:	n/a
17	chr8:34182528-34182578	SK-N-SH_RA	brain:	n/a
18	chr8:34182528-34182578	LNCaP	prostate:	n/a
19	chr8:34182528-34182578	T-47D	breast:	n/a
20	chr8:34182528-34182578	ECC-1	luminal epithelium:	n/a
21	chr8:34182528-34182578	AG09319	gingival:	n/a
22	chr8:34182528-34182578	BE2_C	brain:	n/a
23	chr8:34182528-34182578	HRCEpiC	kidney:	n/a
24	chr8:34182528-34182578	PANC-1	pancreas:	n/a
25	chr8:34182528-34182578	ovcar-3	ovarian:	n/a
26	chr8:34182528-34182578	H1-hESC	embryonic stem cell:	embryo
27	chr8:34182528-34182578	BJ	skin:	n/a
28	chr8:34182528-34182578	SAEC	small airway:	n/a
29	chr8:34182528-34182578	HIPEpiC	eye:	n/a
30	chr8:34182528-34182578	MCF10A-Er-Src	breast:	n/a
31	chr8:34182528-34182578	Jurkat	blood:	n/a
32	chr8:34182528-34182578	AG09309	skin:	n/a
33	chr8:34182528-34182578	K562	blood:	n/a
34	chr8:34182528-34182578	HEK293	kidney:	embryo
35	chr8:34182528-34182578	HCPEpiC	choroid plexus:	n/a
36	chr8:34182528-34182578	HUVEC	blood vessel:	n/a
37	chr8:34182528-34182578	GM12878	blood:	n/a
38	chr8:34182528-34182578	IMR90	lung:	fetal
39	chr8:34182528-34182578	NT2-D1	testis:	n/a
40	chr8:34182528-34182578	AG04450	lung:	fetal
41	chr8:34182528-34182578	GM12892	blood:	n/a
42	chr8:34182528-34182578	Hepatocyte	liver:	n/a
43	chr8:34182528-34182578	GM06990	blood:	n/a
44	chr8:34182528-34182578	HepG2	liver:	n/a
45	chr8:34182528-34182578	Hela-S3	cervix:	n/a
46	chr8:34182528-34182578	SKMC	muscle:	n/a
47	chr8:34182528-34182578	AG10803	skin:	n/a
48	chr8:34182528-34182578	SK-N-SH	brain:	n/a
49	chr8:34182528-34182578	AoSMC	blood vessel:	n/a
50	chr8:34182528-34182578	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:121484907..121485538-chr8:34201775..34202754,2	K562	blood:
2	chr1:121484119..121485425-chr8:34201754..34202754,5	MCF-7	breast:
3	chr19:27736247..27738846-chr8:34200775..34202275,2	MCF-7	breast:
4	chr1:121483557..121485425-chr8:34200754..34202254,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAK16-3	chr8:34197578-34197730	ENSG00000253108
2	lnc-MAK16-3	chr8:34204103-34204249	ENSG00000253108

Variant related genes	Relation type
ENSG00000215264	TF binding region
ENSG00000215264	CpG island

Extended variants
information (count: 881 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:881 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540763946	chr8:34178212-34178213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548981750	chr8:34178241-34178242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558540515	chr8:34178256-34178257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576895023	chr8:34178264-34178265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541151156	chr8:34178292-34178293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78764606	chr8:34178294-34178295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs80121880	chr8:34178311-34178312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144238289	chr8:34178333-34178334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113324638	chr8:34178349-34178350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542899580	chr8:34178358-34178359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561075105	chr8:34178375-34178376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531636917	chr8:34178418-34178419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549757547	chr8:34178433-34178434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564889378	chr8:34178513-34178514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532217476	chr8:34178535-34178536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2719324	chr8:34178569-34178570	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566245952	chr8:34178573-34178574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74910418	chr8:34178659-34178660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548857005	chr8:34178662-34178663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62511613	chr8:34178686-34178687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537766373	chr8:34178689-34178690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200594889	chr8:34178691-34178692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186669275	chr8:34178730-34178731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558503421	chr8:34178742-34178743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141600380	chr8:34178786-34178787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192020720	chr8:34178795-34178796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150902656	chr8:34178811-34178812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs71541875	chr8:34178857-34178858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs398047172	chr8:34178859-34178860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139724451	chr8:34178868-34178869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116173473	chr8:34178870-34178871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369014222	chr8:34178894-34178895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561145920	chr8:34178943-34178944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144379312	chr8:34178949-34178950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543760638	chr8:34178974-34178975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564851283	chr8:34178995-34178996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146113600	chr8:34179028-34179029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558977027	chr8:34179044-34179045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559227945	chr8:34179081-34179082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527888615	chr8:34179115-34179116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529796612	chr8:34179137-34179138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548462460	chr8:34179190-34179191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570254716	chr8:34179196-34179197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550544920	chr8:34179271-34179272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531090361	chr8:34179273-34179274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552487250	chr8:34179280-34179281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555716448	chr8:34179298-34179299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570504854	chr8:34179373-34179374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78991085	chr8:34179415-34179416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2609625	chr8:34179424-34179425	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34178200-34180000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:34179000-34180600	Enhancers	Fetal Intestine Large	intestine
3	chr8:34179400-34180000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:34179600-34180000	Enhancers	Fetal Lung	lung
5	chr8:34180000-34180600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:34180600-34181000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:34181000-34181800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:34181200-34184400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr8:34181800-34182000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:34181800-34182600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:34181800-34184800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:34181800-34185400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:34182000-34182400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:34182000-34184800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:34182000-34185600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:34182200-34182400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:34182200-34182800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:34182200-34183800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:34182400-34182800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:34182400-34183400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:34182600-34183000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr8:34182600-34184000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:34182800-34184000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr8:34182800-34184000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr8:34182800-34184400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:34183000-34184000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr8:34183400-34185400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:34183800-34184000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr8:34184000-34184200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:34184000-34184200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr8:34184000-34184400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:34184000-34184600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr8:34184000-34184800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:34184200-34184400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr8:34184200-34184400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr8:34184400-34184600	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr8:34184400-34186000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:34184400-34195800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr8:34184600-34184800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr8:34185400-34186600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:34186000-34193400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:34192400-34194200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr8:34192600-34193600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr8:34192800-34193600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:34193000-34193600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:34193000-34193600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:34193000-34193800	Enhancers	Brain Germinal Matrix	brain
48	chr8:34193000-34194000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:34193200-34193600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr8:34193200-34193800	Enhancers	HUES64 Cell Line	embryonic stem cell

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