Variant report

Variant	nsv1037003
Chromosome Location	chr12:86610040-86798121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:467)
CpG islands
(count:488)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr12:86624079-86624702	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr12:86705709-86705766	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr12:86617529-86617530	GM12878	blood:	n/a	n/a
6	CEBPB	chr12:86624082-86624737	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:86729535-86729923	A549	lung:	n/a	n/a
8	CEBPB	chr12:86654966-86655213	A549	lung:	n/a	n/a
9	CEBPB	chr12:86716434-86716725	Hela-S3	cervix:	n/a	chr12:86716572-86716585 chr12:86716574-86716585 chr12:86716572-86716585 chr12:86716574-86716585
10	CEBPB	chr12:86760323-86760570	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:86654940-86655288	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:86645972-86646254	HepG2	liver:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
13	CEBPB	chr12:86647213-86647291	HepG2	liver:	n/a	chr12:86647273-86647284
14	CEBPB	chr12:86742139-86742513	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:86736448-86736846	Hela-S3	cervix:	n/a	chr12:86736661-86736673
16	CEBPB	chr12:86760270-86760559	A549	lung:	n/a	n/a
17	CEBPB	chr12:86749345-86749363	K562	blood:	n/a	n/a
18	CEBPB	chr12:86707089-86707289	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:86646079-86646091	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:86654936-86655271	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:86645929-86646233	IMR90	lung:	n/a	chr12:86646082-86646093 chr12:86646081-86646094 chr12:86646081-86646092
22	CEBPB	chr12:86620344-86620573	MCF-7	breast:	n/a	n/a
23	CTCF	chr12:86770020-86770170	HCFaa	heart:	n/a	n/a
24	CTCF	chr12:86770020-86770170	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr12:86658952-86658969	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:86770000-86770150	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:86769997-86770157	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:86769960-86770110	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:86617780-86617930	HEK293	kidney:	n/a	n/a
30	CTCF	chr12:86770040-86770190	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr12:86769960-86770110	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr12:86770020-86770170	HMEC	breast:	n/a	n/a
33	CTCF	chr12:86769980-86770130	HMEC	breast:	n/a	n/a
34	CTCF	chr12:86617880-86618030	GM12878	blood:	n/a	n/a
35	CTCF	chr12:86617840-86617990	HCT-116	colon:	n/a	n/a
36	CTCF	chr12:86770040-86770190	HPF	lung:	n/a	n/a
37	CTCF	chr12:86769920-86770070	HMF	breast:	n/a	n/a
38	CTCF	chr12:86652320-86652470	AG10803	skin:	n/a	n/a
39	CTCF	chr12:86658898-86658932	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:86769940-86770090	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr12:86769960-86770110	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr12:86770000-86770150	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr12:86769960-86770110	SAEC	small airway:	n/a	n/a
44	CTCF	chr12:86787420-86787570	BE2_C	brain:	n/a	n/a
45	CTCF	chr12:86769940-86770090	AG04450	lung:	n/a	n/a
46	CTCF	chr12:86617848-86617963	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr12:86787468-86787487	GM10266	blood:	n/a	n/a
48	CTCF	chr12:86769980-86770130	GM12875	blood:	n/a	n/a
49	CTCF	chr12:86769900-86770050	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr12:86658906-86658951	MCF-7	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86658745-86658795	Jurkat	blood:	n/a
2	chr12:86727874-86727924	CMK	blood:	n/a
3	chr12:86727874-86727924	AG04449	skin:	fetal
4	chr12:86690485-86690535	HCPEpiC	choroid plexus:	n/a
5	chr12:86658745-86658795	NB4	blood:	n/a
6	chr12:86659008-86659058	GM06990	blood:	n/a
7	chr12:86727874-86727924	GM12891	blood:	n/a
8	chr12:86658860-86658910	PFSK-1	brain:	n/a
9	chr12:86658860-86658910	SKMC	muscle:	n/a
10	chr12:86690485-86690535	HMEC	breast:	n/a
11	chr12:86727874-86727924	AG09309	skin:	n/a
12	chr12:86690485-86690535	SK-N-SH_RA	brain:	n/a
13	chr12:86651249-86651299	Hela-S3	cervix:	n/a
14	chr12:86658385-86658435	SK-N-SH_RA	brain:	n/a
15	chr12:86658385-86658435	GM12878	blood:	n/a
16	chr12:86690485-86690535	NH-A	brain:	n/a
17	chr12:86650107-86650157	CMK	blood:	n/a
18	chr12:86727874-86727924	PANC-1	pancreas:	n/a
19	chr12:86658385-86658435	HIPEpiC	eye:	n/a
20	chr12:86690485-86690535	HAEpiC	amniotic membrane:	n/a
21	chr12:86658860-86658910	GM12891	blood:	n/a
22	chr12:86690485-86690535	HCM	heart:	n/a
23	chr12:86658385-86658435	HRPEpiC	eye:	n/a
24	chr12:86658860-86658910	PrEC	prostate:	n/a
25	chr12:86690485-86690535	GM12892	blood:	n/a
26	chr12:86727874-86727924	Caco-2	colon:	n/a
27	chr12:86659008-86659058	SK-N-SH_RA	brain:	n/a
28	chr12:86690485-86690535	HUVEC	blood vessel:	n/a
29	chr12:86659008-86659058	ProgFib	skin:	n/a
30	chr12:86651249-86651299	HIPEpiC	eye:	n/a
31	chr12:86690485-86690535	LNCaP	prostate:	n/a
32	chr12:86651249-86651299	HepG2	liver:	n/a
33	chr12:86659008-86659058	A549	lung:	n/a
34	chr12:86651249-86651299	ECC-1	luminal epithelium:	n/a
35	chr12:86690485-86690535	ECC-1	luminal epithelium:	n/a
36	chr12:86659008-86659058	HNPCEpiC	eye:	n/a
37	chr12:86727874-86727924	HCPEpiC	choroid plexus:	n/a
38	chr12:86690485-86690535	U87	brain:	n/a
39	chr12:86651249-86651299	CMK	blood:	n/a
40	chr12:86727874-86727924	GM12878	blood:	n/a
41	chr12:86690485-86690535	SK-N-MC	brain:	n/a
42	chr12:86727874-86727924	NHBE	bronchial:	n/a
43	chr12:86659008-86659058	LNCaP	prostate:	n/a
44	chr12:86658385-86658435	GM12892	blood:	n/a
45	chr12:86651249-86651299	AG04450	lung:	fetal
46	chr12:86658860-86658910	NH-A	brain:	n/a
47	chr12:86651249-86651299	SK-N-SH	brain:	n/a
48	chr12:86659008-86659058	H1-hESC	embryonic stem cell:	embryo
49	chr12:86659008-86659058	HRCEpiC	kidney:	n/a
50	chr12:86650107-86650157	T-47D	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
2	chr12:86783284..86785651-chr14:104583194..104586028,2	MCF-7	breast:
3	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
4	chr12:86629307..86629807-chr7:120030191..120030808,2	MCF-7	breast:
5	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
6	chr12:86633057..86634931-chr12:86636880..86638760,2	K562	blood:
7	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
8	chr12:86661669..86664440-chr12:86664812..86667661,2	MCF-7	breast:
9	chr12:86626187..86628759-chr12:86629956..86631967,2	K562	blood:
10	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	chr12:86650017-86650192	NONHSAT029760
2	lnc-MGAT4C-1	chr12:86650017-86650101	NONHSAT029763
3	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029759
4	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029762

No data

Variant related genes	Relation type
MGAT4C	TF binding region
MGAT4C	CpG island
ENSG00000207568	chromatin interactions

Extended variants
information (count: 3637 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3637 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183046438	chr12:86611201-86611202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534137605	chr12:86611269-86611270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572960817	chr12:86611289-86611290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570837640	chr12:86611431-86611432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188078409	chr12:86611444-86611445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144429681	chr12:86611500-86611501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12581359	chr12:86611543-86611544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573670425	chr12:86611565-86611566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191170224	chr12:86611584-86611585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563947722	chr12:86611641-86611642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531204640	chr12:86611691-86611692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58654411	chr12:86611751-86611752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182342286	chr12:86611753-86611754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570772420	chr12:86611774-86611775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs61949011	chr12:86611779-86611780	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs58096683	chr12:86611809-86611810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575547456	chr12:86611825-86611826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186613119	chr12:86611831-86611832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535435565	chr12:86611851-86611852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373672586	chr12:86611857-86611858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569175210	chr12:86611890-86611891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374217696	chr12:86611923-86611924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539680397	chr12:86611976-86611977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149952676	chr12:86612006-86612007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572991207	chr12:86612021-86612022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145215460	chr12:86612033-86612034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78966696	chr12:86612097-86612098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73180152	chr12:86612108-86612109	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34335987	chr12:86612158-86612159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544343740	chr12:86612216-86612217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556087728	chr12:86612281-86612282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192626119	chr12:86612287-86612288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371721687	chr12:86612300-86612301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535704467	chr12:86612301-86612302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574393775	chr12:86612329-86612330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184606547	chr12:86612337-86612338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78150020	chr12:86612341-86612342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188406140	chr12:86612366-86612367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572351126	chr12:86612378-86612379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564669817	chr12:86612397-86612398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528672887	chr12:86612399-86612400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs58591163	chr12:86612423-86612424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561967543	chr12:86612524-86612525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11103890	chr12:86612529-86612530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529313854	chr12:86612588-86612589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546057955	chr12:86612637-86612638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550671427	chr12:86612668-86612669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193014210	chr12:86612695-86612696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149137461	chr12:86612763-86612764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185145160	chr12:86612800-86612801	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86611200-86613600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:86614000-86625600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:86615800-86616200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:86616200-86618400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:86619000-86620200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:86620200-86620600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:86620600-86622800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:86622200-86622800	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr12:86622200-86624800	Enhancers	HUVEC	blood vessel
10	chr12:86622600-86622800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:86622600-86625400	Enhancers	Hela-S3	cervix
12	chr12:86622800-86623800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:86622800-86623800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:86622800-86624000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr12:86623600-86624600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:86623800-86624000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr12:86623800-86624000	Enhancers	A549	lung
18	chr12:86623800-86624600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:86623800-86625000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:86623800-86625000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr12:86623800-86625000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:86623800-86625200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr12:86623800-86625400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:86623800-86625800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:86624000-86624400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr12:86624000-86624800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:86624000-86625000	Enhancers	NH-A	brain
28	chr12:86624000-86625200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr12:86624000-86625200	Flanking Active TSS	A549	lung
30	chr12:86624200-86624600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr12:86624200-86624600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:86624200-86625000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:86624200-86625200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:86624400-86624600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:86624400-86625200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:86624600-86625200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr12:86624600-86626200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:86624600-86627000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:86624600-86627800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:86624800-86625200	Flanking Active TSS	HUVEC	blood vessel
41	chr12:86625000-86626200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:86625000-86626200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:86625000-86627000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:86625200-86625400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr12:86625200-86625400	Enhancers	Brain Germinal Matrix	brain
46	chr12:86625200-86625400	Enhancers	A549	lung
47	chr12:86625200-86625800	Enhancers	HUVEC	blood vessel
48	chr12:86625200-86626200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr12:86625200-86626200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr12:86625400-86625800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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