Variant report

Variant	nsv999796
Chromosome Location	chr3:79762461-79938163
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	chr3:79895393-79895705	HepG2	liver:	n/a	n/a
2	BACH1	chr3:79815463-79816887	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr3:79875120-79875138	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr3:79893061-79893185	A549	lung:	n/a	n/a
5	CEBPB	chr3:79792370-79792570	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:79895428-79895613	HepG2	liver:	n/a	chr3:79895546-79895557
7	CEBPB	chr3:79805850-79806038	H1-hESC	embryonic stem cell:	n/a	chr3:79805873-79805884
8	CEBPB	chr3:79895411-79895612	MCF-7	breast:	n/a	chr3:79895546-79895557
9	CEBPB	chr3:79921627-79921962	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:79773324-79773772	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:79895392-79895631	A549	lung:	n/a	chr3:79895546-79895557
12	CEBPB	chr3:79921554-79922186	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:79805807-79806044	HepG2	liver:	n/a	chr3:79805873-79805884
14	CEBPB	chr3:79805720-79806054	A549	lung:	n/a	chr3:79805873-79805884
15	CEBPB	chr3:79773393-79773804	MCF-7	breast:	n/a	n/a
16	CEBPB	chr3:79895338-79895728	HepG2	liver:	n/a	chr3:79895546-79895557
17	CEBPB	chr3:79805787-79806055	K562	blood:	n/a	chr3:79805873-79805884
18	CEBPB	chr3:79921641-79922161	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:79921618-79922085	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:79805711-79806054	IMR90	lung:	n/a	chr3:79805873-79805884
21	CHD2	chr3:79789666-79789843	HepG2	liver:	n/a	n/a
22	CTCF	chr3:79773560-79773710	HRE	kidney:	n/a	n/a
23	CTCF	chr3:79773424-79773623	Medullo	brain:	n/a	n/a
24	CTCF	chr3:79816140-79816290	HPF	lung:	n/a	chr3:79816209-79816217
25	CTCF	chr3:79773494-79773516	LNCaP	prostate:	n/a	n/a
26	CTCF	chr3:79895780-79895930	HUVEC	blood vessel:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
27	CTCF	chr3:79773420-79773570	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr3:79895860-79896010	GM12864	blood:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
29	CTCF	chr3:79773426-79773799	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:79906312-79906359	GM20000	blood:	n/a	n/a
31	CTCF	chr3:79895800-79895950	HVMF	connective:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
32	CTCF	chr3:79895840-79895990	HPF	lung:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
33	CTCF	chr3:79895860-79896010	NHEK	skin:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
34	CTCF	chr3:79773504-79773592	GM13977	blood:	n/a	n/a
35	CTCF	chr3:79839445-79839574	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:79895800-79895950	AG04450	lung:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
37	CTCF	chr3:79839429-79839611	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:79816640-79816790	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr3:79773440-79773590	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr3:79895817-79895992	Hela-S3	cervix:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
41	CTCF	chr3:79839360-79839510	GM12872	blood:	n/a	n/a
42	CTCF	chr3:79895760-79895910	HepG2	liver:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
43	CTCF	chr3:79895673-79896092	H1-hESC	embryonic stem cell:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
44	CTCF	chr3:79778300-79778450	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr3:79895800-79895950	GM12869	blood:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
46	CTCF	chr3:79895730-79896073	K562	blood:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
47	CTCF	chr3:79839518-79839614	GM13977	blood:	n/a	n/a
48	CTCF	chr3:79895798-79896018	Medullo	brain:	n/a	chr3:79895893-79895906 chr3:79895892-79895908 chr3:79895894-79895904 chr3:79895891-79895909
49	CTCF	chr3:79839440-79839616	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:79839420-79839570	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:79816794-79816844	AG09309	skin:	n/a
2	chr3:79817232-79817282	NHBE	bronchial:	n/a
3	chr3:79815782-79815832	GM12892	blood:	n/a
4	chr3:79818505-79818555	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:79817333-79817383	AG10803	skin:	n/a
6	chr3:79817333-79817383	Caco-2	colon:	n/a
7	chr3:79816309-79816359	SK-N-SH	brain:	n/a
8	chr3:79815848-79815898	Hepatocyte	liver:	n/a
9	chr3:79816309-79816359	NHDF-neo	bronchial:	n/a
10	chr3:79816309-79816359	LNCaP	prostate:	n/a
11	chr3:79816838-79816888	Hepatocyte	liver:	n/a
12	chr3:79818505-79818555	HIPEpiC	eye:	n/a
13	chr3:79817333-79817383	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:79817125-79817175	HCT-116	colon:	n/a
15	chr3:79817278-79817328	HPAEpiC	pulmonary alveolar:	n/a
16	chr3:79817333-79817383	HCT-116	colon:	n/a
17	chr3:79818505-79818555	HCPEpiC	choroid plexus:	n/a
18	chr3:79817125-79817175	AG10803	skin:	n/a
19	chr3:79816794-79816844	HUVEC	blood vessel:	n/a
20	chr3:79815639-79815689	A549	lung:	n/a
21	chr3:79815639-79815689	GM12892	blood:	n/a
22	chr3:79818505-79818555	HUVEC	blood vessel:	n/a
23	chr3:79815639-79815689	ovcar-3	ovarian:	n/a
24	chr3:79816949-79816999	ovcar-3	ovarian:	n/a
25	chr3:79815782-79815832	HAEpiC	amniotic membrane:	n/a
26	chr3:79816949-79816999	T-47D	breast:	n/a
27	chr3:79817333-79817383	GM12878	blood:	n/a
28	chr3:79816838-79816888	HCT-116	colon:	n/a
29	chr3:79815718-79815768	GM19239	blood:	n/a
30	chr3:79817278-79817328	GM12891	blood:	n/a
31	chr3:79816794-79816844	HAEpiC	amniotic membrane:	n/a
32	chr3:79815718-79815768	ovcar-3	ovarian:	n/a
33	chr3:79817333-79817383	HRPEpiC	eye:	n/a
34	chr3:79816838-79816888	GM19239	blood:	n/a
35	chr3:79816949-79816999	AoSMC	blood vessel:	n/a
36	chr3:79816838-79816888	NT2-D1	testis:	n/a
37	chr3:79817125-79817175	BE2_C	brain:	n/a
38	chr3:79816794-79816844	HEEpiC	esophagus:	n/a
39	chr3:79814509-79814559	SK-N-SH	brain:	n/a
40	chr3:79814509-79814559	GM06990	blood:	n/a
41	chr3:79816949-79816999	H1-hESC	embryonic stem cell:	embryo
42	chr3:79815848-79815898	MCF10A-Er-Src	breast:	n/a
43	chr3:79816794-79816844	HIPEpiC	eye:	n/a
44	chr3:79815639-79815689	LNCaP	prostate:	n/a
45	chr3:79815718-79815768	HMEC	breast:	n/a
46	chr3:79815782-79815832	GM19239	blood:	n/a
47	chr3:79816794-79816844	GM12892	blood:	n/a
48	chr3:79815639-79815689	AG04450	lung:	fetal
49	chr3:79816949-79816999	HCT-116	colon:	n/a
50	chr3:79815639-79815689	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:79852227..79853757-chr3:79856920..79859314,2	MCF-7	breast:
2	chr3:79898588..79900974-chr3:79908884..79910528,2	K562	blood:
3	chr3:79861656..79863360-chr3:79921900..79923820,2	MCF-7	breast:
4	chr3:79853639..79855426-chr3:79859362..79861187,2	MCF-7	breast:
5	chr3:79852227..79853757-chr3:79856920..79859314,2	MCF-7	breast:
6	chr3:79898588..79900974-chr3:79908884..79910528,2	K562	blood:
7	chr3:79892706..79894533-chr3:79898255..79901019,2	MCF-7	breast:
8	chr3:79936013..79938678-chr3:79939132..79941923,2	MCF-7	breast:
9	chr3:79892706..79894533-chr3:79898255..79901019,2	MCF-7	breast:
10	chr3:79805055..79807269-chr3:79815015..79816845,2	K562	blood:
11	chr3:79570076..79571010-chr3:79773148..79773748,2	MCF-7	breast:
12	chr3:79917063..79919514-chr3:79920813..79923055,2	MCF-7	breast:
13	chr3:79836046..79838934-chr3:79839908..79842507,2	MCF-7	breast:
14	chr3:79568902..79571189-chr3:79767488..79770126,2	K562	blood:
15	chr3:79861656..79863360-chr3:79921900..79923820,2	MCF-7	breast:
16	chr1:149223298..149225198-chr3:79807270..79809196,2	MCF-7	breast:
17	chr3:79917063..79919514-chr3:79920813..79923055,2	MCF-7	breast:
18	chr3:79821220..79822809-chr3:79822885..79824428,2	MCF-7	breast:
19	chr3:79925894..79927399-chr3:79928694..79930422,2	MCF-7	breast:
20	chr20:50831774..50832427-chr3:79921398..79922155,2	MCF-7	breast:
21	chr3:79836046..79838934-chr3:79839908..79842507,2	MCF-7	breast:
22	chr3:79853639..79855426-chr3:79859362..79861187,2	MCF-7	breast:
23	chr3:79805055..79807269-chr3:79815015..79816845,2	K562	blood:
24	chr3:79925894..79927399-chr3:79928694..79930422,2	MCF-7	breast:
25	chr3:79821220..79822809-chr3:79822885..79824428,2	MCF-7	breast:

Variant related genes	Relation type
ROBO1	TF binding region
ROBO1	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 1801 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538309304	chr3:79776098-79776099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570890337	chr3:79776124-79776125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186847737	chr3:79776159-79776160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571442478	chr3:79776188-79776189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533924081	chr3:79776202-79776203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191688749	chr3:79776206-79776207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12638741	chr3:79776224-79776225	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541766803	chr3:79776277-79776278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73849825	chr3:79776323-79776324	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs75061088	chr3:79776324-79776325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544444434	chr3:79776338-79776339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554593063	chr3:79776400-79776401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115301366	chr3:79778206-79778207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193129273	chr3:79778207-79778208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531609528	chr3:79778218-79778219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79220023	chr3:79778228-79778229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549858157	chr3:79778264-79778265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571602230	chr3:79778265-79778266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183944392	chr3:79778308-79778309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7613917	chr3:79778355-79778356	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs547717017	chr3:79778371-79778372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188444076	chr3:79778450-79778451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536353788	chr3:79778456-79778457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140384057	chr3:79778457-79778458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35341351	chr3:79778596-79778597	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs554829854	chr3:79778607-79778608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150383152	chr3:79778646-79778647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558808667	chr3:79778658-79778659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79782966	chr3:79778659-79778660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541260555	chr3:79778666-79778667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75043175	chr3:79778703-79778704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74354341	chr3:79778726-79778727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138810117	chr3:79778733-79778734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149800184	chr3:79778745-79778746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563801479	chr3:79778761-79778762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193033230	chr3:79778782-79778783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552647775	chr3:79778791-79778792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377268447	chr3:79778793-79778794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571565253	chr3:79778833-79778834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527589062	chr3:79778858-79778859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547236145	chr3:79778877-79778878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567468328	chr3:79778971-79778972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535936414	chr3:79779038-79779039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370508213	chr3:79779049-79779050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184196671	chr3:79779075-79779076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77073520	chr3:79779080-79779081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538237022	chr3:79779094-79779095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141988152	chr3:79779168-79779169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572357010	chr3:79779181-79779182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188871526	chr3:79779225-79779226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:79776000-79776400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:79778200-79778400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:79778200-79779200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr3:79778400-79778800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:79778600-79779200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:79779000-79779200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:79779200-79780200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr3:79780400-79780600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:79783600-79784000	Enhancers	Fetal Brain Male	brain
10	chr3:79811200-79811800	Active TSS	Primary hematopoietic stem cells	blood
11	chr3:79812000-79812200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr3:79814000-79814200	Enhancers	Brain Germinal Matrix	brain
13	chr3:79814000-79815000	Enhancers	Fetal Brain Male	brain
14	chr3:79814000-79818000	Active TSS	Fetal Brain Female	brain
15	chr3:79814200-79814400	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr3:79814200-79814400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr3:79814200-79815400	Enhancers	Ovary	ovary
18	chr3:79814400-79814800	Enhancers	Brain Germinal Matrix	brain
19	chr3:79814800-79815000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:79814800-79815000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
21	chr3:79814800-79815200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr3:79814800-79815200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr3:79814800-79815600	Flanking Active TSS	Brain Germinal Matrix	brain
24	chr3:79815000-79815200	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
25	chr3:79815000-79815200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:79815000-79815200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr3:79815000-79815200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr3:79815000-79815200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
29	chr3:79815000-79815200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:79815000-79815400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr3:79815000-79815400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:79815000-79815400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:79815000-79815400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr3:79815000-79815600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr3:79815000-79815600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
36	chr3:79815000-79816000	Active TSS	Brain Anterior Caudate	brain
37	chr3:79815000-79816000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
38	chr3:79815000-79816000	Flanking Active TSS	Fetal Brain Male	brain
39	chr3:79815000-79817600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr3:79815200-79815400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
41	chr3:79815200-79815400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:79815200-79815400	Bivalent Enhancer	HUVEC	blood vessel
43	chr3:79815200-79815600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr3:79815200-79815600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
45	chr3:79815200-79815600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
46	chr3:79815200-79815800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:79815200-79816200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
48	chr3:79815200-79816400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr3:79815200-79816800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
50	chr3:79815200-79817000	Bivalent/Poised TSS	NH-A	brain

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