Variant report

Variant	nsv557527
Chromosome Location	chr12:11481057-11557659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:366)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

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	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
6	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
8	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
9	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
10	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
11	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
12	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
13	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
14	CTCF	chr12:11500820-11500970	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr12:11544846-11544963	GM13976	blood:	n/a	n/a
16	CTCF	chr12:11500840-11500990	NHEK	skin:	n/a	n/a
17	CTCF	chr12:11506052-11506137	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:11500860-11500982	LNCaP	prostate:	n/a	n/a
20	CTCF	chr12:11529002-11529034	GM10266	blood:	n/a	n/a
21	CTCF	chr12:11505592-11505641	GM20000	blood:	n/a	n/a
22	CTCF	chr12:11500860-11501010	GM12864	blood:	n/a	n/a
23	CTCF	chr12:11500800-11500950	GM12865	blood:	n/a	n/a
24	CTCF	chr12:11500880-11501030	HVMF	connective:	n/a	n/a
25	CTCF	chr12:11500820-11500970	GM12873	blood:	n/a	n/a
26	CTCF	chr12:11500840-11500990	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr12:11500840-11500990	GM12865	blood:	n/a	n/a
28	CTCF	chr12:11500539-11501299	A549	lung:	n/a	n/a
29	CTCF	chr12:11528342-11528385	LNCaP	prostate:	n/a	n/a
30	CTCF	chr12:11545750-11545873	GM13977	blood:	n/a	n/a
31	CTCF	chr12:11500860-11501010	GM12874	blood:	n/a	n/a
32	CTCF	chr12:11506036-11506126	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:11500840-11500990	HPF	lung:	n/a	n/a
34	CTCF	chr12:11506054-11506114	GM10266	blood:	n/a	n/a
35	CTCF	chr12:11500900-11501050	GM12868	blood:	n/a	n/a
36	CTCF	chr12:11500900-11501050	RPTEC	kidney:	n/a	n/a
37	CTCF	chr12:11500907-11500926	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:11501529-11501579	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:11501680-11501830	GM12866	blood:	n/a	n/a
40	CTCF	chr12:11500840-11500990	HMF	breast:	n/a	n/a
41	CTCF	chr12:11490383-11490444	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr12:11500820-11500970	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:11548407-11548506	Lung_OC	lung:	n/a	n/a
44	CTCF	chr12:11500820-11500970	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr12:11500880-11501030	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr12:11506136-11506201	GM20000	blood:	n/a	n/a
47	CTCF	chr12:11545746-11545856	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:11500820-11500970	HMF	breast:	n/a	n/a
49	CTCF	chr12:11500920-11501070	HMEC	breast:	n/a	n/a
50	CTCF	chr12:11492997-11493057	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11549192-11549242	GM12878	blood:	n/a
2	chr12:11548019-11548069	GM12892	blood:	n/a
3	chr12:11549555-11549605	HepG2	liver:	n/a
4	chr12:11509583-11509633	IMR90	lung:	fetal
5	chr12:11548019-11548069	HRCEpiC	kidney:	n/a
6	chr12:11509583-11509633	Jurkat	blood:	n/a
7	chr12:11549192-11549242	Hela-S3	cervix:	n/a
8	chr12:11548867-11548917	A549	lung:	n/a
9	chr12:11549555-11549605	MCF10A-Er-Src	breast:	n/a
10	chr12:11508049-11508099	MCF-7	breast:	n/a
11	chr12:11549555-11549605	HEEpiC	esophagus:	n/a
12	chr12:11509583-11509633	SKMC	muscle:	n/a
13	chr12:11549192-11549242	HMEC	breast:	n/a
14	chr12:11549192-11549242	MCF10A-Er-Src	breast:	n/a
15	chr12:11508049-11508099	SK-N-MC	brain:	n/a
16	chr12:11549192-11549242	HCT-116	colon:	n/a
17	chr12:11509583-11509633	CMK	blood:	n/a
18	chr12:11508049-11508099	A549	lung:	n/a
19	chr12:11508049-11508099	AG04449	skin:	fetal
20	chr12:11548867-11548917	PANC-1	pancreas:	n/a
21	chr12:11549192-11549242	A549	lung:	n/a
22	chr12:11549192-11549242	AG04450	lung:	fetal
23	chr12:11548019-11548069	PrEC	prostate:	n/a
24	chr12:11508049-11508099	Jurkat	blood:	n/a
25	chr12:11549192-11549242	SK-N-SH_RA	brain:	n/a
26	chr12:11509583-11509633	AG09319	gingival:	n/a
27	chr12:11549555-11549605	HIPEpiC	eye:	n/a
28	chr12:11548019-11548069	PFSK-1	brain:	n/a
29	chr12:11509583-11509633	GM06990	blood:	n/a
30	chr12:11509583-11509633	HCM	heart:	n/a
31	chr12:11509583-11509633	AoSMC	blood vessel:	n/a
32	chr12:11549192-11549242	HCM	heart:	n/a
33	chr12:11549192-11549242	CMK	blood:	n/a
34	chr12:11549192-11549242	HL-60	blood:	n/a
35	chr12:11548867-11548917	BJ	skin:	n/a
36	chr12:11548867-11548917	CMK	blood:	n/a
37	chr12:11509583-11509633	HAEpiC	amniotic membrane:	n/a
38	chr12:11548019-11548069	ECC-1	luminal epithelium:	n/a
39	chr12:11549192-11549242	H1-hESC	embryonic stem cell:	embryo
40	chr12:11549192-11549242	PANC-1	pancreas:	n/a
41	chr12:11508049-11508099	SKMC	muscle:	n/a
42	chr12:11548867-11548917	Caco-2	colon:	n/a
43	chr12:11549192-11549242	U87	brain:	n/a
44	chr12:11508049-11508099	GM06990	blood:	n/a
45	chr12:11548867-11548917	NHBE	bronchial:	n/a
46	chr12:11549192-11549242	NH-A	brain:	n/a
47	chr12:11548019-11548069	ovcar-3	ovarian:	n/a
48	chr12:11549555-11549605	U87	brain:	n/a
49	chr12:11548019-11548069	NT2-D1	testis:	n/a
50	chr12:11549555-11549605	SK-N-MC	brain:	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: 3103 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3103 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10047526	chr12:11481057-11481058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577319698	chr12:11481066-11481067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561468083	chr12:11481106-11481107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10047527	chr12:11481107-11481108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs75510675	chr12:11481114-11481115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564089231	chr12:11481116-11481117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61928947	chr12:11481177-11481178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192678345	chr12:11481301-11481302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560050754	chr12:11481345-11481346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575976470	chr12:11481393-11481394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548763764	chr12:11481412-11481413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568493540	chr12:11481431-11481432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185478469	chr12:11481434-11481435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12367016	chr12:11481452-11481453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550744384	chr12:11481501-11481502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561791824	chr12:11481504-11481505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72477468	chr12:11481509-11481510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs188803285	chr12:11481513-11481514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149240271	chr12:11481542-11481543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535284169	chr12:11481550-11481551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79657875	chr12:11481565-11481566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568032777	chr12:11481570-11481571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112892915	chr12:11481637-11481638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541185587	chr12:11481645-11481646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575273913	chr12:11481679-11481680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544294154	chr12:11481680-11481681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563968670	chr12:11481681-11481682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192940045	chr12:11481684-11481685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540204414	chr12:11481692-11481693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560101595	chr12:11481694-11481695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374913258	chr12:11481707-11481708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528777606	chr12:11481708-11481709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79880167	chr12:11481741-11481742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562303309	chr12:11481790-11481791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530946935	chr12:11481823-11481824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564338277	chr12:11481857-11481858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185181158	chr12:11481886-11481887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368458947	chr12:11481892-11481893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570810730	chr12:11481949-11481950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533488197	chr12:11481964-11481965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539470624	chr12:11482012-11482013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143465541	chr12:11482042-11482043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148006362	chr12:11482070-11482071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141683339	chr12:11482078-11482079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555321231	chr12:11482119-11482120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575389387	chr12:11482127-11482128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537605737	chr12:11482137-11482138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61583144	chr12:11482145-11482146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577775784	chr12:11482152-11482153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540262510	chr12:11482160-11482161	Weak transcription	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:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11479200-11493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:11486800-11487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:11497200-11497800	Enhancers	HepG2	liver
10	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
11	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel
13	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
14	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
18	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
19	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
21	chr12:11513000-11513800	Enhancers	HMEC	breast
22	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:11513000-11514000	Enhancers	NHEK	skin
24	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:11516600-11517000	Enhancers	HepG2	liver
28	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
39	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
40	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:11550000-11550600	Enhancers	HUVEC	blood vessel
42	chr12:11550000-11550800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr12:11550000-11551000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr12:11550200-11550800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr12:11550200-11550800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr12:11550200-11551000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr12:11550800-11551600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr12:11550800-11568400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr12:11551600-11551800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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