Variant report

Variant	nsv534038
Chromosome Location	chr3:60781917-60993082
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	chr3:60952698-60953635	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:60826899-60827442	HepG2	liver:	n/a	n/a
3	BATF	chr3:60798279-60798572	GM12878	blood:	n/a	chr3:60798453-60798464
4	BHLHE40	chr3:60978219-60978349	K562	blood:	n/a	n/a
5	BHLHE40	chr3:60975976-60976102	K562	blood:	n/a	n/a
6	BRCA1	chr3:60987420-60987425	GM12878	blood:	n/a	n/a
7	CBX3	chr3:60921319-60921862	HCT-116	colon:	n/a	chr3:60921818-60921829
8	CCNT2	chr3:60975948-60976272	K562	blood:	n/a	n/a
9	CCNT2	chr3:60972227-60972556	K562	blood:	n/a	n/a
10	CEBPB	chr3:60805231-60805319	K562	blood:	n/a	chr3:60805273-60805282 chr3:60805273-60805282 chr3:60805271-60805284 chr3:60805273-60805284 chr3:60805271-60805282 chr3:60805271-60805284 chr3:60805273-60805284 chr3:60805273-60805282 chr3:60805273-60805282
11	CEBPB	chr3:60827136-60827432	A549	lung:	n/a	chr3:60827319-60827336
12	CEBPB	chr3:60827089-60827338	HepG2	liver:	n/a	chr3:60827319-60827336
13	CEBPB	chr3:60812519-60812606	H1-hESC	embryonic stem cell:	n/a	chr3:60812568-60812581 chr3:60812568-60812579 chr3:60812568-60812579
14	CEBPB	chr3:60795660-60795869	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:60952811-60953332	HepG2	liver:	n/a	chr3:60953284-60953297
16	CEBPB	chr3:60795601-60795961	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:60826993-60827500	HepG2	liver:	n/a	chr3:60827319-60827336
18	CEBPB	chr3:60863006-60863244	MCF-7	breast:	n/a	chr3:60863087-60863098
19	CEBPB	chr3:60795597-60795965	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:60862936-60863252	H1-hESC	embryonic stem cell:	n/a	chr3:60863087-60863098
21	CEBPB	chr3:60794781-60795064	HepG2	liver:	n/a	chr3:60794924-60794935
22	CEBPB	chr3:60795646-60795932	K562	blood:	n/a	n/a
23	CEBPB	chr3:60827138-60827466	HepG2	liver:	n/a	chr3:60827319-60827336
24	CEBPB	chr3:60862973-60863244	HepG2	liver:	n/a	chr3:60863087-60863098
25	CEBPB	chr3:60795584-60795966	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:60827074-60827475	A549	lung:	n/a	chr3:60827319-60827336
27	CEBPB	chr3:60795630-60795879	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:60826950-60827481	MCF-7	breast:	n/a	chr3:60827319-60827336
29	CEBPB	chr3:60823658-60823891	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:60812393-60812748	HepG2	liver:	n/a	chr3:60812568-60812581 chr3:60812568-60812579 chr3:60812568-60812579
31	CEBPB	chr3:60795445-60796117	MCF-7	breast:	n/a	n/a
32	CEBPB	chr3:60794905-60795022	K562	blood:	n/a	chr3:60794924-60794935
33	CEBPB	chr3:60827100-60827487	HepG2	liver:	n/a	chr3:60827319-60827336
34	CEBPB	chr3:60812447-60812703	A549	lung:	n/a	chr3:60812568-60812581 chr3:60812568-60812579 chr3:60812568-60812579
35	CEBPB	chr3:60795629-60795932	A549	lung:	n/a	n/a
36	CEBPB	chr3:60794803-60795103	IMR90	lung:	n/a	chr3:60794924-60794935
37	CEBPB	chr3:60799895-60800056	K562	blood:	n/a	n/a
38	CEBPB	chr3:60795620-60795952	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr3:60812412-60812683	ECC-1	luminal epithelium:	n/a	chr3:60812568-60812581 chr3:60812568-60812579 chr3:60812568-60812579
40	CEBPB	chr3:60795531-60796022	MCF-7	breast:	n/a	n/a
41	CEBPB	chr3:60805150-60805407	HepG2	liver:	n/a	chr3:60805273-60805282 chr3:60805273-60805282 chr3:60805271-60805284 chr3:60805273-60805284 chr3:60805271-60805282 chr3:60805271-60805284 chr3:60805273-60805284 chr3:60805273-60805282 chr3:60805273-60805282
42	CEBPB	chr3:60862954-60863154	A549	lung:	n/a	chr3:60863087-60863098
43	CEBPB	chr3:60826911-60827588	MCF-7	breast:	n/a	chr3:60827319-60827336
44	CEBPB	chr3:60795588-60795967	HepG2	liver:	n/a	n/a
45	CEBPD	chr3:60891893-60892237	K562	blood:	n/a	n/a
46	CHD2	chr3:60952944-60953139	HepG2	liver:	n/a	n/a
47	CTCF	chr3:60862973-60863189	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:60934315-60934414	Kidney_OC	kidney:	n/a	chr3:60934356-60934369 chr3:60934356-60934369 chr3:60934349-60934370 chr3:60934360-60934369
49	CTCF	chr3:60825005-60825154	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:60825080-60825230	RPTEC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:60818194-60818244	HAEpiC	amniotic membrane:	n/a
2	chr3:60818194-60818244	HAEpiC	amniotic membrane:	n/a
3	chr3:60818194-60818244	T-47D	breast:	n/a
4	chr3:60913404-60913454	SKMC	muscle:	n/a
5	chr3:60913404-60913454	LNCaP	prostate:	n/a
6	chr3:60913404-60913454	HL-60	blood:	n/a
7	chr3:60913404-60913454	AG04449	skin:	fetal
8	chr3:60913404-60913454	Hepatocyte	liver:	n/a
9	chr3:60913404-60913454	NB4	blood:	n/a
10	chr3:60818194-60818244	HRE	kidney:	n/a
11	chr3:60818194-60818244	NH-A	brain:	n/a
12	chr3:60913404-60913454	ovcar-3	ovarian:	n/a
13	chr3:60818194-60818244	HEK293	kidney:	embryo
14	chr3:60913404-60913454	HCF	heart:	n/a
15	chr3:60913404-60913454	HEK293	kidney:	embryo
16	chr3:60818194-60818244	NB4	blood:	n/a
17	chr3:60913404-60913454	HRCEpiC	kidney:	n/a
18	chr3:60818194-60818244	HIPEpiC	eye:	n/a
19	chr3:60913404-60913454	GM06990	blood:	n/a
20	chr3:60818194-60818244	HNPCEpiC	eye:	n/a
21	chr3:60818194-60818244	SK-N-MC	brain:	n/a
22	chr3:60913404-60913454	CMK	blood:	n/a
23	chr3:60913404-60913454	Caco-2	colon:	n/a
24	chr3:60818194-60818244	AG10803	skin:	n/a
25	chr3:60818194-60818244	PFSK-1	brain:	n/a
26	chr3:60913404-60913454	ProgFib	skin:	n/a
27	chr3:60818194-60818244	H1-hESC	embryonic stem cell:	embryo
28	chr3:60913404-60913454	NH-A	brain:	n/a
29	chr3:60913404-60913454	Jurkat	blood:	n/a
30	chr3:60818194-60818244	AG04450	lung:	fetal
31	chr3:60818194-60818244	U87	brain:	n/a
32	chr3:60818194-60818244	K562	blood:	n/a
33	chr3:60818194-60818244	HMEC	breast:	n/a
34	chr3:60913404-60913454	PANC-1	pancreas:	n/a
35	chr3:60913404-60913454	HCT-116	colon:	n/a
36	chr3:60818194-60818244	SAEC	small airway:	n/a
37	chr3:60818194-60818244	HL-60	blood:	n/a
38	chr3:60913404-60913454	HMEC	breast:	n/a
39	chr3:60913404-60913454	MCF-7	breast:	n/a
40	chr3:60913404-60913454	U87	brain:	n/a
41	chr3:60818194-60818244	BJ	skin:	n/a
42	chr3:60818194-60818244	AG09319	gingival:	n/a
43	chr3:60913404-60913454	Hela-S3	cervix:	n/a
44	chr3:60818194-60818244	Hela-S3	cervix:	n/a
45	chr3:60913404-60913454	HRPEpiC	eye:	n/a
46	chr3:60913404-60913454	SK-N-MC	brain:	n/a
47	chr3:60818194-60818244	MCF10A-Er-Src	breast:	n/a
48	chr3:60913404-60913454	SK-N-SH	brain:	n/a
49	chr3:60818194-60818244	HepG2	liver:	n/a
50	chr3:60913404-60913454	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:60924570..60926089-chr3:60929535..60931529,2	K562	blood:
2	chr3:60973639..60975889-chr3:60980470..60983301,2	MCF-7	breast:
3	chr20:52815778..52818231-chr3:60835539..60838352,2	MCF-7	breast:
4	chr3:60788618..60790358-chr3:60795094..60797575,2	K562	blood:
5	chr3:60788618..60790358-chr3:60795094..60797575,2	K562	blood:
6	chr3:60973639..60975889-chr3:60980470..60983301,2	MCF-7	breast:
7	chr3:60955729..60956229-chr8:43092430..43093268,2	MCF-7	breast:
8	chr3:60567788..60568640-chr3:60933917..60934730,2	MCF-7	breast:
9	chr3:60669436..60671802-chr3:60824320..60825859,2	MCF-7	breast:
10	chr3:60917588..60920198-chr3:60923789..60925680,2	K562	blood:
11	chr3:60924570..60926089-chr3:60929535..60931529,2	K562	blood:
12	chr3:60917588..60920198-chr3:60923789..60925680,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FEZF2-6	chr3:60923447-60924934	NONHSAT090164
2	lnc-FEZF2-9	chr3:60807613-60807705	NONHSAT090160
3	lnc-FEZF2-7	chr3:60842062-60842277	NONHSAT090163

Variant related genes	Relation type
ENSG00000212211	TF binding region
ENSG00000212211	CpG island

Extended variants
information (count: 6947 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6947 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554060477	chr3:60781965-60781966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572078446	chr3:60781972-60781973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139729157	chr3:60781980-60781981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9754707	chr3:60782006-60782007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs149801360	chr3:60782015-60782016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386661522	chr3:60782030-60782031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192247396	chr3:60782067-60782068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2736731	chr3:60782102-60782103	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2594171	chr3:60782122-60782123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561963581	chr3:60782127-60782128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552357422	chr3:60782159-60782160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573871232	chr3:60782190-60782191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541331349	chr3:60782203-60782204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2594170	chr3:60782218-60782219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533409713	chr3:60782247-60782248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542254394	chr3:60782307-60782308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200513221	chr3:60782315-60782316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533928256	chr3:60782319-60782320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551462118	chr3:60782320-60782321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184271722	chr3:60782343-60782344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530921026	chr3:60782361-60782362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145783275	chr3:60782380-60782381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2594169	chr3:60782381-60782382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs535604389	chr3:60782410-60782411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547756079	chr3:60782428-60782429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554321496	chr3:60782437-60782438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565834691	chr3:60782474-60782475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375905319	chr3:60782477-60782478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188830838	chr3:60782484-60782485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575960870	chr3:60782506-60782507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567914309	chr3:60782516-60782517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2594168	chr3:60782560-60782561	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191749515	chr3:60782561-60782562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541221448	chr3:60782567-60782568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559646489	chr3:60782696-60782697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578174150	chr3:60782708-60782709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184721656	chr3:60782713-60782714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563553904	chr3:60782715-60782716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530887032	chr3:60782732-60782733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2594167	chr3:60782743-60782744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561358250	chr3:60782757-60782758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529148874	chr3:60782774-60782775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75746932	chr3:60782791-60782792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79490770	chr3:60782794-60782795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76427343	chr3:60782795-60782796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547593860	chr3:60782809-60782810	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565999003	chr3:60782814-60782815	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78682814	chr3:60782833-60782834	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531514340	chr3:60782839-60782840	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549684220	chr3:60782857-60782858	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Autism	22102821	CNVD
Prostate cancer	19363497	CNVD
Malaria	21533027	CNVD
Colorectal cancer	21518781	CNVD
Esophageal cancer	21518781	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD
Bipolar disorder	19114987	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60767000-60782800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:60778800-60787800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:60782800-60783400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:60782800-60784400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr3:60784400-60787000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:60784600-60785200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:60785200-60787200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:60786800-60789200	Enhancers	Brain Germinal Matrix	brain
9	chr3:60787000-60787400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr3:60787000-60789200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr3:60787000-60789200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr3:60787200-60789200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:60787400-60788000	Enhancers	Fetal Lung	lung
14	chr3:60787800-60789200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr3:60788000-60789000	Enhancers	Fetal Brain Male	brain
16	chr3:60788800-60790000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:60788800-60790000	Active TSS	Brain Angular Gyrus	brain
18	chr3:60788800-60790000	Active TSS	Brain Cingulate Gyrus	brain
19	chr3:60788800-60790200	Active TSS	Brain Anterior Caudate	brain
20	chr3:60788800-60790200	Active TSS	Brain Hippocampus Middle	brain
21	chr3:60788800-60790200	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr3:60789000-60789200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr3:60789000-60790200	Active TSS	Brain Substantia Nigra	brain
24	chr3:60789000-60790200	Bivalent Enhancer	Fetal Brain Male	brain
25	chr3:60789000-60790200	Active TSS	Fetal Brain Female	brain
26	chr3:60789200-60789600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr3:60789200-60789600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:60789200-60790000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:60789200-60790000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:60789200-60790000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr3:60789200-60790200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr3:60789200-60790200	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr3:60789600-60789800	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr3:60789600-60790000	Enhancers	NHDF-Ad	bronchial
35	chr3:60789600-60790800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:60789800-60790000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr3:60790000-60790200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:60790000-60790200	Enhancers	Brain Angular Gyrus	brain
39	chr3:60790000-60790200	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr3:60790000-60791200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:60790200-60790800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr3:60790200-60790800	Enhancers	Brain Germinal Matrix	brain
43	chr3:60790200-60792400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:60790800-60792400	Weak transcription	Brain Germinal Matrix	brain
45	chr3:60790800-60794400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr3:60790800-60795400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:60792400-60793200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:60792400-60793400	Enhancers	Brain Germinal Matrix	brain
49	chr3:60793200-60794000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr3:60794200-60798600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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