Variant report

Variant	nsv898790
Chromosome Location	chr12:11476725-11557659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:367)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:11501400-11501725	K562	blood:	n/a	n/a
2	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:11478711-11479007	HepG2	liver:	n/a	chr12:11478828-11478841 chr12:11478830-11478839 chr12:11478828-11478839 chr12:11478829-11478840
6	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
7	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
8	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
9	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
11	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
12	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
13	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
14	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
15	CTCF	chr12:11500780-11500930	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr12:11500900-11501050	GM12864	blood:	n/a	n/a
17	CTCF	chr12:11500858-11500977	GM12878	blood:	n/a	n/a
18	CTCF	chr12:11548407-11548506	Lung_OC	lung:	n/a	n/a
19	CTCF	chr12:11500800-11500950	SAEC	small airway:	n/a	n/a
20	CTCF	chr12:11531414-11531456	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr12:11500860-11501010	GM12873	blood:	n/a	n/a
22	CTCF	chr12:11500840-11500990	AG04450	lung:	n/a	n/a
23	CTCF	chr12:11505990-11506144	K562	blood:	n/a	n/a
24	CTCF	chr12:11545775-11545832	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:11500860-11501010	Caco-2	colon:	n/a	n/a
26	CTCF	chr12:11501529-11501579	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:11500766-11501020	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11500920-11501070	GM12872	blood:	n/a	n/a
29	CTCF	chr12:11500840-11500990	GM12875	blood:	n/a	n/a
30	CTCF	chr12:11500800-11500950	GM12874	blood:	n/a	n/a
31	CTCF	chr12:11500880-11501030	HVMF	connective:	n/a	n/a
32	CTCF	chr12:11545671-11545700	GM10266	blood:	n/a	n/a
33	CTCF	chr12:11506021-11506166	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr12:11500880-11501030	GM12869	blood:	n/a	n/a
35	CTCF	chr12:11501578-11501581	A549	lung:	n/a	n/a
36	CTCF	chr12:11500689-11501045	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr12:11500860-11501010	GM12872	blood:	n/a	n/a
38	CTCF	chr12:11524600-11524750	GM12865	blood:	n/a	n/a
39	CTCF	chr12:11506052-11506137	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:11552280-11552316	GM13977	blood:	n/a	n/a
41	CTCF	chr12:11505978-11506004	Lung_OC	lung:	n/a	n/a
42	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:11500820-11500970	RPTEC	kidney:	n/a	n/a
44	CTCF	chr12:11500880-11501030	GM06990	blood:	n/a	n/a
45	CTCF	chr12:11500820-11500970	GM12801	blood:	n/a	n/a
46	CTCF	chr12:11500874-11501000	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr12:11500800-11500950	GM12871	blood:	n/a	n/a
48	CTCF	chr12:11500920-11501070	AG04450	lung:	n/a	n/a
49	CTCF	chr12:11508581-11508633	GM13976	blood:	n/a	n/a
50	CTCF	chr12:11545778-11545816	GM12891	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11548867-11548917	GM12892	blood:	n/a
2	chr12:11548867-11548917	GM12892	blood:	n/a
3	chr12:11549192-11549242	HCT-116	colon:	n/a
4	chr12:11508049-11508099	HAEpiC	amniotic membrane:	n/a
5	chr12:11508049-11508099	H1-hESC	embryonic stem cell:	embryo
6	chr12:11549555-11549605	NB4	blood:	n/a
7	chr12:11549192-11549242	Hela-S3	cervix:	n/a
8	chr12:11549555-11549605	K562	blood:	n/a
9	chr12:11508049-11508099	PFSK-1	brain:	n/a
10	chr12:11509583-11509633	GM19239	blood:	n/a
11	chr12:11549192-11549242	ProgFib	skin:	n/a
12	chr12:11549555-11549605	AG04450	lung:	fetal
13	chr12:11549192-11549242	HRE	kidney:	n/a
14	chr12:11549555-11549605	HEK293	kidney:	embryo
15	chr12:11509583-11509633	PANC-1	pancreas:	n/a
16	chr12:11549555-11549605	Caco-2	colon:	n/a
17	chr12:11508049-11508099	GM12892	blood:	n/a
18	chr12:11549192-11549242	T-47D	breast:	n/a
19	chr12:11549192-11549242	GM12892	blood:	n/a
20	chr12:11548019-11548069	ECC-1	luminal epithelium:	n/a
21	chr12:11548019-11548069	PANC-1	pancreas:	n/a
22	chr12:11549555-11549605	PFSK-1	brain:	n/a
23	chr12:11548867-11548917	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:11549192-11549242	Caco-2	colon:	n/a
25	chr12:11549555-11549605	SAEC	small airway:	n/a
26	chr12:11509583-11509633	ovcar-3	ovarian:	n/a
27	chr12:11509583-11509633	SK-N-SH_RA	brain:	n/a
28	chr12:11508049-11508099	NHBE	bronchial:	n/a
29	chr12:11549192-11549242	AG04450	lung:	fetal
30	chr12:11548867-11548917	SK-N-SH_RA	brain:	n/a
31	chr12:11548867-11548917	LNCaP	prostate:	n/a
32	chr12:11508049-11508099	NB4	blood:	n/a
33	chr12:11549192-11549242	AG09319	gingival:	n/a
34	chr12:11509583-11509633	RPTEC	kidney:	n/a
35	chr12:11508049-11508099	NT2-D1	testis:	n/a
36	chr12:11508049-11508099	Hepatocyte	liver:	n/a
37	chr12:11508049-11508099	SK-N-SH_RA	brain:	n/a
38	chr12:11549192-11549242	SK-N-SH_RA	brain:	n/a
39	chr12:11549555-11549605	CMK	blood:	n/a
40	chr12:11549192-11549242	SKMC	muscle:	n/a
41	chr12:11548019-11548069	A549	lung:	n/a
42	chr12:11549555-11549605	AoSMC	blood vessel:	n/a
43	chr12:11548867-11548917	CMK	blood:	n/a
44	chr12:11548019-11548069	GM06990	blood:	n/a
45	chr12:11549555-11549605	HL-60	blood:	n/a
46	chr12:11548019-11548069	AG09319	gingival:	n/a
47	chr12:11548867-11548917	HRPEpiC	eye:	n/a
48	chr12:11548019-11548069	ProgFib	skin:	n/a
49	chr12:11549555-11549605	HMEC	breast:	n/a
50	chr12:11508049-11508099	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
2	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1
2	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
3	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1

No data

Variant related genes	Relation type
PRB2	TF binding region
PRB1	TF binding region
PRB2	CpG island
PRB1	CpG island

Extended variants
information (count: 3359 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3359 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10845332	chr12:11476725-11476726	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561530926	chr12:11476740-11476741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374079971	chr12:11476760-11476761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111379012	chr12:11476769-11476770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560992679	chr12:11476774-11476775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564152468	chr12:11476817-11476818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532801882	chr12:11476859-11476860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151111541	chr12:11476883-11476884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566267350	chr12:11476895-11476896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528777671	chr12:11476909-11476910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142664094	chr12:11476925-11476926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568664687	chr12:11476956-11476957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537580567	chr12:11477029-11477030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557183993	chr12:11477030-11477031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570877074	chr12:11477070-11477071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529704438	chr12:11477081-11477082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553296499	chr12:11477093-11477094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572836663	chr12:11477113-11477114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4763681	chr12:11477123-11477124	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs202072322	chr12:11477137-11477138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113378839	chr12:11477141-11477142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555190149	chr12:11477148-11477149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186285254	chr12:11477149-11477150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543964789	chr12:11477153-11477154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79224910	chr12:11477159-11477160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564031837	chr12:11477186-11477187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12099553	chr12:11477187-11477188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571970656	chr12:11477279-11477280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117871579	chr12:11477307-11477308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189635951	chr12:11477342-11477343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117273764	chr12:11477360-11477361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528838808	chr12:11477401-11477402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540677193	chr12:11477409-11477410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568729980	chr12:11477442-11477443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560188974	chr12:11477457-11477458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531131602	chr12:11477495-11477496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183415157	chr12:11477500-11477501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6488392	chr12:11477514-11477515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6488393	chr12:11477535-11477536	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs553121790	chr12:11477541-11477542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144613677	chr12:11477555-11477556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535401180	chr12:11477565-11477566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555253759	chr12:11477579-11477580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76060689	chr12:11477597-11477598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186341357	chr12:11477606-11477607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147879699	chr12:11477612-11477613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548877453	chr12:11477616-11477617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190783775	chr12:11477650-11477651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540318122	chr12:11477657-11477658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559929974	chr12:11477689-11477690	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11475400-11478200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:11478200-11479200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr12:11478800-11479400	Enhancers	HMEC	breast
4	chr12:11479000-11479200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:11479200-11480200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr12:11479200-11493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:11486800-11487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:11497200-11497800	Enhancers	HepG2	liver
15	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
16	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel
18	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
19	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
23	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
24	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
26	chr12:11513000-11513800	Enhancers	HMEC	breast
27	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:11513000-11514000	Enhancers	NHEK	skin
29	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:11516600-11517000	Enhancers	HepG2	liver
33	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
44	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
45	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr12:11550000-11550600	Enhancers	HUVEC	blood vessel
47	chr12:11550000-11550800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:11550000-11551000	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr12:11550200-11550800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr12:11550200-11550800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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