Variant report

Variant	nsv541565
Chromosome Location	chr12:86616015-86733418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:489)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:86643692-86643942	GM12878	blood:	n/a	n/a
2	BATF	chr12:86643693-86643934	GM12878	blood:	n/a	n/a
3	BRCA1	chr12:86705709-86705766	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr12:86617529-86617530	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:86624079-86624702	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:86646079-86646091	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr12:86645972-86646254	HepG2	liver:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
8	CEBPB	chr12:86716434-86716725	Hela-S3	cervix:	n/a	chr12:86716572-86716585 chr12:86716574-86716585 chr12:86716572-86716585 chr12:86716574-86716585
9	CEBPB	chr12:86654940-86655288	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:86729535-86729923	A549	lung:	n/a	n/a
11	CEBPB	chr12:86654966-86655213	A549	lung:	n/a	n/a
12	CEBPB	chr12:86707089-86707289	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:86620344-86620573	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:86647213-86647291	HepG2	liver:	n/a	chr12:86647273-86647284
15	CEBPB	chr12:86645929-86646233	IMR90	lung:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
16	CEBPB	chr12:86624082-86624737	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:86654936-86655271	IMR90	lung:	n/a	n/a
18	CTCF	chr12:86617869-86617939	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:86658898-86658932	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:86658292-86658348	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:86652320-86652470	AG10803	skin:	n/a	n/a
22	CTCF	chr12:86696271-86696316	ProgFib	skin:	n/a	n/a
23	CTCF	chr12:86719551-86719594	A549	lung:	n/a	n/a
24	CTCF	chr12:86617740-86617890	HAc	cerebellar:	n/a	n/a
25	CTCF	chr12:86617720-86617870	BE2_C	brain:	n/a	n/a
26	CTCF	chr12:86658620-86658770	SAEC	small airway:	n/a	n/a
27	CTCF	chr12:86617840-86617990	HCT-116	colon:	n/a	n/a
28	CTCF	chr12:86690624-86690689	GM13976	blood:	n/a	n/a
29	CTCF	chr12:86617880-86617907	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr12:86658247-86658371	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:86643680-86643830	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr12:86617780-86617930	HEK293	kidney:	n/a	n/a
33	CTCF	chr12:86617860-86618010	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr12:86658952-86658969	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:86658906-86658951	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:86617800-86617950	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr12:86617800-86617950	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr12:86617820-86617970	HepG2	liver:	n/a	n/a
39	CTCF	chr12:86617800-86617950	HRE	kidney:	n/a	n/a
40	CTCF	chr12:86617848-86617963	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:86617880-86618030	GM12878	blood:	n/a	n/a
42	E2F4	chr12:86652235-86652336	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr12:86654976-86655318	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr12:86716434-86716644	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr12:86699919-86700118	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr12:86680671-86681053	GM12878	blood:	n/a	n/a
47	EBF1	chr12:86643633-86643900	GM12878	blood:	n/a	chr12:86643773-86643784
48	EBF1	chr12:86643661-86643889	GM12878	blood:	n/a	chr12:86643773-86643784
49	EBF1	chr12:86680730-86681018	GM12878	blood:	n/a	n/a
50	EBF1	chr12:86643368-86643996	GM12878	blood:	n/a	chr12:86643773-86643784

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86650107-86650157	HMEC	breast:	n/a
2	chr12:86650107-86650157	HMEC	breast:	n/a
3	chr12:86659008-86659058	NH-A	brain:	n/a
4	chr12:86690485-86690535	HepG2	liver:	n/a
5	chr12:86650107-86650157	T-47D	breast:	n/a
6	chr12:86727874-86727924	HL-60	blood:	n/a
7	chr12:86650107-86650157	NHBE	bronchial:	n/a
8	chr12:86651249-86651299	SKMC	muscle:	n/a
9	chr12:86650107-86650157	Hepatocyte	liver:	n/a
10	chr12:86658745-86658795	AG04449	skin:	fetal
11	chr12:86651249-86651299	HEK293	kidney:	embryo
12	chr12:86650107-86650157	K562	blood:	n/a
13	chr12:86658385-86658435	HAEpiC	amniotic membrane:	n/a
14	chr12:86658860-86658910	Caco-2	colon:	n/a
15	chr12:86727874-86727924	GM19239	blood:	n/a
16	chr12:86690485-86690535	HRCEpiC	kidney:	n/a
17	chr12:86658745-86658795	AG04450	lung:	fetal
18	chr12:86727874-86727924	ECC-1	luminal epithelium:	n/a
19	chr12:86690485-86690535	PFSK-1	brain:	n/a
20	chr12:86690485-86690535	BE2_C	brain:	n/a
21	chr12:86658745-86658795	HL-60	blood:	n/a
22	chr12:86658385-86658435	IMR90	lung:	fetal
23	chr12:86658745-86658795	HRPEpiC	eye:	n/a
24	chr12:86658745-86658795	NB4	blood:	n/a
25	chr12:86650107-86650157	Caco-2	colon:	n/a
26	chr12:86690485-86690535	HUVEC	blood vessel:	n/a
27	chr12:86658860-86658910	SK-N-SH_RA	brain:	n/a
28	chr12:86658385-86658435	SAEC	small airway:	n/a
29	chr12:86650107-86650157	HNPCEpiC	eye:	n/a
30	chr12:86658745-86658795	HMEC	breast:	n/a
31	chr12:86658745-86658795	AG09319	gingival:	n/a
32	chr12:86651249-86651299	PrEC	prostate:	n/a
33	chr12:86650107-86650157	PANC-1	pancreas:	n/a
34	chr12:86659008-86659058	HMEC	breast:	n/a
35	chr12:86658745-86658795	GM12878	blood:	n/a
36	chr12:86650107-86650157	HEK293	kidney:	embryo
37	chr12:86658385-86658435	HCF	heart:	n/a
38	chr12:86651249-86651299	GM12892	blood:	n/a
39	chr12:86727874-86727924	HMEC	breast:	n/a
40	chr12:86658385-86658435	HRCEpiC	kidney:	n/a
41	chr12:86658745-86658795	GM06990	blood:	n/a
42	chr12:86658860-86658910	HCF	heart:	n/a
43	chr12:86651249-86651299	RPTEC	kidney:	n/a
44	chr12:86690485-86690535	HRE	kidney:	n/a
45	chr12:86690485-86690535	HEEpiC	esophagus:	n/a
46	chr12:86658385-86658435	PrEC	prostate:	n/a
47	chr12:86658860-86658910	HL-60	blood:	n/a
48	chr12:86658860-86658910	A549	lung:	n/a
49	chr12:86658745-86658795	PANC-1	pancreas:	n/a
50	chr12:86658745-86658795	BE2_C	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
2	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
3	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
4	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
5	chr12:86629307..86629807-chr7:120030191..120030808,2	MCF-7	breast:
6	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
7	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
8	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029759
2	lnc-MGAT4C-1	chr12:86650017-86650192	NONHSAT029760
3	lnc-MGAT4C-1	chr12:86650017-86650101	NONHSAT029763
4	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029762

No data

Variant related genes	Relation type
MGAT4C	TF binding region
MGAT4C	CpG island

Extended variants
information (count: 2752 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2752 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576872671	chr12:86616018-86616019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532385595	chr12:86616019-86616020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140425621	chr12:86616063-86616064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565469594	chr12:86616091-86616092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs61949013	chr12:86616092-86616093	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547752623	chr12:86616104-86616105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189237806	chr12:86616106-86616107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs207473216	chr12:86616150-86616151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576219492	chr12:86616192-86616193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144281504	chr12:86616234-86616235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556817925	chr12:86616273-86616274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs193077081	chr12:86616293-86616294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34079580	chr12:86616333-86616334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539256866	chr12:86616392-86616393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73387513	chr12:86616433-86616434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73387516	chr12:86616450-86616451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543159270	chr12:86616482-86616483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183800403	chr12:86616490-86616491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188289941	chr12:86616524-86616525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543351727	chr12:86616580-86616581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565226276	chr12:86616613-86616614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532190630	chr12:86616621-86616622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540852792	chr12:86616726-86616727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369047929	chr12:86616763-86616764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191849302	chr12:86616796-86616797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539736622	chr12:86616799-86616800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529706206	chr12:86616804-86616805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372569981	chr12:86616846-86616847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569503175	chr12:86616857-86616858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370877054	chr12:86616898-86616899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530573296	chr12:86616950-86616951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541827584	chr12:86616953-86616954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550192318	chr12:86616978-86616979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571937630	chr12:86616984-86616985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538985868	chr12:86617003-86617004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554373047	chr12:86617027-86617028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566289136	chr12:86617044-86617045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536700627	chr12:86617112-86617113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555149032	chr12:86617124-86617125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576350454	chr12:86617142-86617143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543832476	chr12:86617146-86617147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147413184	chr12:86617157-86617158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375854123	chr12:86617164-86617165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375432150	chr12:86617177-86617178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139651450	chr12:86617217-86617218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560474801	chr12:86617234-86617235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184027143	chr12:86617236-86617237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559080555	chr12:86617268-86617269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537800504	chr12:86617272-86617273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529842408	chr12:86617295-86617296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86614000-86625600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:86615800-86616200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:86616200-86618400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:86619000-86620200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:86620200-86620600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:86620600-86622800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:86622200-86622800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr12:86622200-86624800	Enhancers	HUVEC	blood vessel
9	chr12:86622600-86622800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:86622600-86625400	Enhancers	Hela-S3	cervix
11	chr12:86622800-86623800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:86622800-86623800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:86622800-86624000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr12:86623600-86624600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr12:86623800-86624000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr12:86623800-86624000	Enhancers	A549	lung
17	chr12:86623800-86624600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr12:86623800-86625000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:86623800-86625000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr12:86623800-86625000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:86623800-86625200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:86623800-86625400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:86623800-86625800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:86624000-86624400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr12:86624000-86624800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr12:86624000-86625000	Enhancers	NH-A	brain
27	chr12:86624000-86625200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr12:86624000-86625200	Flanking Active TSS	A549	lung
29	chr12:86624200-86624600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr12:86624200-86624600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr12:86624200-86625000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:86624200-86625200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr12:86624400-86624600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr12:86624400-86625200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr12:86624600-86625200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr12:86624600-86626200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr12:86624600-86627000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr12:86624600-86627800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:86624800-86625200	Flanking Active TSS	HUVEC	blood vessel
40	chr12:86625000-86626200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:86625000-86626200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr12:86625000-86627000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr12:86625200-86625400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr12:86625200-86625400	Enhancers	Brain Germinal Matrix	brain
45	chr12:86625200-86625400	Enhancers	A549	lung
46	chr12:86625200-86625800	Enhancers	HUVEC	blood vessel
47	chr12:86625200-86626200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr12:86625200-86626200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr12:86625400-86625800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:86625400-86626400	Weak transcription	Brain Germinal Matrix	brain

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