Variant report

Variant	nsv526146
Chromosome Location	chr12:29989292-30112823
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:30074366-30074532	K562	blood:	n/a	n/a
2	ATF2	chr12:30037909-30038322	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:30037896-30038293	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:30037174-30037384	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:30011309-30011494	GM12878	blood:	n/a	n/a
6	BATF	chr12:29998207-29998406	GM12878	blood:	n/a	chr12:29998338-29998349
7	BATF	chr12:30011854-30012105	GM12878	blood:	n/a	chr12:30012002-30012013
8	BCL11A	chr12:30037980-30038278	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr12:30037917-30038252	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr12:30083094-30083126	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:30011251-30011451	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:30035579-30035745	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr12:30042695-30042991	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:30037981-30038350	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:30097586-30097898	IMR90	lung:	n/a	n/a
16	CEBPB	chr12:30073337-30073369	HepG2	liver:	n/a	chr12:30073350-30073361
17	CEBPB	chr12:30097554-30097899	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:30042693-30042986	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:30109122-30109385	A549	lung:	n/a	chr12:30109282-30109293
20	CEBPB	chr12:30097575-30097889	A549	lung:	n/a	n/a
21	CEBPB	chr12:30073678-30073947	IMR90	lung:	n/a	chr12:30073815-30073826 chr12:30073817-30073826
22	CEBPB	chr12:30030003-30030203	HepG2	liver:	n/a	chr12:30030066-30030077
23	CEBPB	chr12:30109117-30109423	HepG2	liver:	n/a	chr12:30109282-30109293
24	CEBPB	chr12:30009767-30009887	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:30073708-30073951	HepG2	liver:	n/a	chr12:30073815-30073826 chr12:30073817-30073826
26	CEBPB	chr12:30009784-30009882	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:30097592-30097854	HepG2	liver:	n/a	n/a
28	CHD1	chr12:30001143-30001184	GM12878	blood:	n/a	n/a
29	CHD1	chr12:29991136-29991204	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr12:30037916-30038373	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr12:30020929-30020939	K562	blood:	n/a	n/a
32	CHD2	chr12:30042718-30043019	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr12:30032183-30032581	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr12:29997760-29997910	HCFaa	heart:	n/a	n/a
35	CTCF	chr12:30042740-30042890	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr12:30042637-30043021	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:30042716-30042977	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr12:30042728-30042963	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:30042780-30042930	GM12872	blood:	n/a	n/a
40	CTCF	chr12:29997740-29997890	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr12:30054700-30054850	GM12871	blood:	n/a	chr12:30054741-30054757 chr12:30054735-30054756
42	CTCF	chr12:30042780-30042930	AG09309	skin:	n/a	n/a
43	CTCF	chr12:30042691-30042965	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr12:30054641-30054828	Hela-S3	cervix:	n/a	chr12:30054741-30054757 chr12:30054735-30054756
45	CTCF	chr12:30042720-30042870	GM12865	blood:	n/a	n/a
46	CTCF	chr12:30042793-30042933	GM20000	blood:	n/a	n/a
47	CTCF	chr12:30087578-30087614	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr12:30042800-30042950	AG04450	lung:	n/a	n/a
49	CTCF	chr12:30042800-30042950	HCT-116	colon:	n/a	n/a
50	CTCF	chr12:30042740-30042890	HEEpiC	esophagus:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30032232-30032282	BJ	skin:	n/a
2	chr12:30032232-30032282	NH-A	brain:	n/a
3	chr12:30032232-30032282	NB4	blood:	n/a
4	chr12:30032232-30032282	PFSK-1	brain:	n/a
5	chr12:30032232-30032282	Jurkat	blood:	n/a
6	chr12:30016391-30016441	GM12892	blood:	n/a
7	chr12:30032232-30032282	HCT-116	colon:	n/a
8	chr12:30032232-30032282	NHBE	bronchial:	n/a
9	chr12:30016391-30016441	HMEC	breast:	n/a
10	chr12:30016391-30016441	U87	brain:	n/a
11	chr12:30016391-30016441	HRE	kidney:	n/a
12	chr12:30032232-30032282	HL-60	blood:	n/a
13	chr12:30032232-30032282	AG04450	lung:	fetal
14	chr12:30016391-30016441	HAEpiC	amniotic membrane:	n/a
15	chr12:30032232-30032282	T-47D	breast:	n/a
16	chr12:30016391-30016441	SK-N-SH	brain:	n/a
17	chr12:30032232-30032282	ECC-1	luminal epithelium:	n/a
18	chr12:30016391-30016441	T-47D	breast:	n/a
19	chr12:30016391-30016441	GM12878	blood:	n/a
20	chr12:30016391-30016441	HEEpiC	esophagus:	n/a
21	chr12:30016391-30016441	A549	lung:	n/a
22	chr12:30016391-30016441	LNCaP	prostate:	n/a
23	chr12:30032232-30032282	Hela-S3	cervix:	n/a
24	chr12:30032232-30032282	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:30016391-30016441	CMK	blood:	n/a
26	chr12:30032232-30032282	RPTEC	kidney:	n/a
27	chr12:30016391-30016441	NH-A	brain:	n/a
28	chr12:30016391-30016441	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:30016391-30016441	HEK293	kidney:	embryo
30	chr12:30032232-30032282	GM12891	blood:	n/a
31	chr12:30032232-30032282	NHDF-neo	bronchial:	n/a
32	chr12:30016391-30016441	MCF10A-Er-Src	breast:	n/a
33	chr12:30016391-30016441	AG09309	skin:	n/a
34	chr12:30032232-30032282	PrEC	prostate:	n/a
35	chr12:30032232-30032282	AG04449	skin:	fetal
36	chr12:30016391-30016441	NHDF-neo	bronchial:	n/a
37	chr12:30016391-30016441	PrEC	prostate:	n/a
38	chr12:30016391-30016441	HCM	heart:	n/a
39	chr12:30016391-30016441	RPTEC	kidney:	n/a
40	chr12:30016391-30016441	ovcar-3	ovarian:	n/a
41	chr12:30016391-30016441	GM06990	blood:	n/a
42	chr12:30032232-30032282	SK-N-MC	brain:	n/a
43	chr12:30016391-30016441	SK-N-MC	brain:	n/a
44	chr12:30032232-30032282	AoSMC	blood vessel:	n/a
45	chr12:30032232-30032282	AG09319	gingival:	n/a
46	chr12:30016391-30016441	Jurkat	blood:	n/a
47	chr12:30032232-30032282	AG09309	skin:	n/a
48	chr12:30032232-30032282	GM19239	blood:	n/a
49	chr12:30016391-30016441	PANC-1	pancreas:	n/a
50	chr12:30016391-30016441	AG04450	lung:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:30029795..30032959-chr12:30033915..30036859,3	K562	blood:
2	chr12:29995160..29997764-chr12:29998716..30001221,2	MCF-7	breast:
3	chr12:30093971..30096199-chr12:30100888..30102830,2	MCF-7	breast:
4	chr12:30012273..30014244-chr12:30025832..30028070,2	MCF-7	breast:
5	chr12:30107931..30110000-chr12:30112088..30114969,2	K562	blood:
6	chr12:30093971..30096199-chr12:30100888..30102830,2	MCF-7	breast:
7	chr12:30012273..30014244-chr12:30025832..30028070,2	MCF-7	breast:
8	chr12:29995160..29997764-chr12:29998716..30001221,2	MCF-7	breast:
9	chr12:30029795..30032959-chr12:30033915..30036859,3	K562	blood:
10	chr12:30048962..30051425-chr12:30054034..30055862,2	MCF-7	breast:
11	chr12:30007730..30010615-chr3:183415263..183417934,2	MCF-7	breast:
12	chr12:30048962..30051425-chr12:30054034..30055862,2	MCF-7	breast:
13	chr12:30107931..30110000-chr12:30112088..30114969,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253052	TF binding region
ENSG00000253052	CpG island
ENSG00000163872	chromatin interactions

Extended variants
information (count: 3653 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3653 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190205976	chr12:29991629-29991630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529456322	chr12:29991639-29991640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs448334	chr12:29991642-29991643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs75557932	chr12:29991675-29991676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558600898	chr12:29991676-29991677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551354681	chr12:29991677-29991678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566575541	chr12:29991706-29991707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534017042	chr12:29991734-29991735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554984527	chr12:29991738-29991739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574070155	chr12:29991740-29991741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537996994	chr12:29991752-29991753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12306578	chr12:29991763-29991764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs572427423	chr12:29991796-29991797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113305576	chr12:29991816-29991817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545368215	chr12:29991823-29991824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141317768	chr12:29991889-29991890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572042046	chr12:29991891-29991892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542274318	chr12:29991922-29991923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566900291	chr12:29991925-29991926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35795005	chr12:29991927-29991928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537584142	chr12:29991953-29991954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146606735	chr12:29991976-29991977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562786082	chr12:29991977-29991978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113834077	chr12:29991996-29991997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181501936	chr12:29992063-29992064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558802236	chr12:29992070-29992071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566836073	chr12:29992092-29992093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534166692	chr12:29992124-29992125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147902531	chr12:29992152-29992153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186112342	chr12:29992166-29992167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535452100	chr12:29992186-29992187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144785509	chr12:29992187-29992188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190137323	chr12:29992194-29992195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556389546	chr12:29992200-29992201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577939626	chr12:29992260-29992261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538919510	chr12:29992265-29992266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576943652	chr12:29992302-29992303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540735643	chr12:29992347-29992348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554074804	chr12:29992351-29992352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114241521	chr12:29992371-29992372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544108772	chr12:29992449-29992450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368755476	chr12:29992453-29992454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554279608	chr12:29992469-29992470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576080452	chr12:29992475-29992476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1595527	chr12:29992505-29992506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs415456	chr12:29992528-29992529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182794744	chr12:29992569-29992570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562603567	chr12:29992601-29992602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1595525	chr12:29992609-29992610	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562592548	chr12:29992686-29992687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29991600-29997600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:29994000-29994200	Enhancers	Fetal Lung	lung
3	chr12:29994000-29996600	Enhancers	Fetal Brain Male	brain
4	chr12:29994200-29995000	Weak transcription	Fetal Lung	lung
5	chr12:29995000-29998000	Enhancers	Fetal Lung	lung
6	chr12:29996000-29996200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:29996200-30003000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:29996400-29996600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr12:29996600-29997600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr12:29997600-29998000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr12:29997600-29998200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:29997600-29998400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr12:29997800-29998400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:29997800-29998400	Enhancers	HSMMtube	muscle
15	chr12:30001400-30001800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:30008400-30014400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr12:30011200-30011800	Enhancers	Fetal Brain Female	brain
18	chr12:30011200-30011800	Enhancers	NHEK	skin
19	chr12:30011200-30012000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:30011200-30012000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:30011400-30012000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:30011400-30012800	Enhancers	HMEC	breast
23	chr12:30014400-30016800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr12:30016000-30017600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
25	chr12:30016200-30016800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
26	chr12:30016200-30017200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr12:30016400-30017200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr12:30016600-30016800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr12:30016800-30018200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr12:30017000-30017200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
31	chr12:30017000-30017400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
32	chr12:30018200-30023600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr12:30020200-30027000	Weak transcription	Fetal Kidney	kidney
34	chr12:30022800-30023000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:30022800-30024000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:30022800-30024200	Enhancers	Fetal Lung	lung
37	chr12:30023000-30023800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:30023000-30024200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:30023000-30024400	Enhancers	Fetal Stomach	stomach
40	chr12:30023000-30032400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:30023600-30024200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr12:30023600-30024400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr12:30023600-30024400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr12:30024200-30026400	Weak transcription	Fetal Lung	lung
45	chr12:30024200-30032400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:30024400-30027000	Weak transcription	Fetal Stomach	stomach
47	chr12:30026400-30027800	Enhancers	Fetal Lung	lung
48	chr12:30027000-30027200	Enhancers	Fetal Stomach	stomach
49	chr12:30027000-30027600	Enhancers	Fetal Kidney	kidney
50	chr12:30031000-30031200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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