Variant report

Variant	nsv1036331
Chromosome Location	chr12:11493164-11581762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:366)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 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	CBX3	chr12:11569521-11569734	K562	blood:	n/a	n/a
5	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
8	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
9	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
10	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
11	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
12	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
13	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
14	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
15	CTCF	chr12:11556054-11556104	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:11505592-11505641	GM20000	blood:	n/a	n/a
17	CTCF	chr12:11500840-11500990	HMF	breast:	n/a	n/a
18	CTCF	chr12:11552280-11552316	GM13977	blood:	n/a	n/a
19	CTCF	chr12:11500860-11501010	Caco-2	colon:	n/a	n/a
20	CTCF	chr12:11501525-11501558	Fibrobl	skin:	n/a	n/a
21	CTCF	chr12:11500880-11501030	HCT-116	colon:	n/a	n/a
22	CTCF	chr12:11500880-11501030	HMEC	breast:	n/a	n/a
23	CTCF	chr12:11566785-11566861	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr12:11500873-11500995	K562	blood:	n/a	n/a
25	CTCF	chr12:11500840-11500990	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr12:11500800-11500950	GM12871	blood:	n/a	n/a
27	CTCF	chr12:11549867-11549930	GM13976	blood:	n/a	n/a
28	CTCF	chr12:11500860-11501010	GM06990	blood:	n/a	n/a
29	CTCF	chr12:11500900-11501050	RPTEC	kidney:	n/a	n/a
30	CTCF	chr12:11500860-11501010	GM12874	blood:	n/a	n/a
31	CTCF	chr12:11500780-11500930	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr12:11500720-11500870	BE2_C	brain:	n/a	n/a
33	CTCF	chr12:11545778-11545816	GM12891	blood:	n/a	n/a
34	CTCF	chr12:11500820-11500970	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:11500840-11500990	GM12870	blood:	n/a	n/a
36	CTCF	chr12:11506054-11506114	GM10266	blood:	n/a	n/a
37	CTCF	chr12:11501520-11501609	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:11501578-11501581	A549	lung:	n/a	n/a
39	CTCF	chr12:11500900-11501050	GM12878	blood:	n/a	n/a
40	CTCF	chr12:11501587-11501601	A549	lung:	n/a	n/a
41	CTCF	chr12:11500920-11501070	WI-38	lung:	n/a	n/a
42	CTCF	chr12:11506021-11506166	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:11500860-11501010	GM12872	blood:	n/a	n/a
44	CTCF	chr12:11500800-11500950	GM12865	blood:	n/a	n/a
45	CTCF	chr12:11500800-11500950	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr12:11500840-11500990	GM12872	blood:	n/a	n/a
47	CTCF	chr12:11500780-11500930	Caco-2	colon:	n/a	n/a
48	CTCF	chr12:11500820-11500970	HMF	breast:	n/a	n/a
49	CTCF	chr12:11544846-11544963	GM13976	blood:	n/a	n/a
50	CTCF	chr12:11545746-11545856	MCF-7	breast:	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	GM12892	blood:	n/a
2	chr12:11548867-11548917	AG10803	skin:	n/a
3	chr12:11509583-11509633	AoSMC	blood vessel:	n/a
4	chr12:11509583-11509633	AG10803	skin:	n/a
5	chr12:11549555-11549605	GM12892	blood:	n/a
6	chr12:11549192-11549242	AG09309	skin:	n/a
7	chr12:11509583-11509633	HCT-116	colon:	n/a
8	chr12:11549555-11549605	HCT-116	colon:	n/a
9	chr12:11508049-11508099	HMEC	breast:	n/a
10	chr12:11548867-11548917	H1-hESC	embryonic stem cell:	embryo
11	chr12:11548867-11548917	BJ	skin:	n/a
12	chr12:11548019-11548069	NT2-D1	testis:	n/a
13	chr12:11549555-11549605	SAEC	small airway:	n/a
14	chr12:11549555-11549605	Hepatocyte	liver:	n/a
15	chr12:11509583-11509633	AG09309	skin:	n/a
16	chr12:11508049-11508099	AoSMC	blood vessel:	n/a
17	chr12:11548867-11548917	HCT-116	colon:	n/a
18	chr12:11508049-11508099	AG04449	skin:	fetal
19	chr12:11509583-11509633	K562	blood:	n/a
20	chr12:11549555-11549605	NHBE	bronchial:	n/a
21	chr12:11508049-11508099	GM19239	blood:	n/a
22	chr12:11509583-11509633	ovcar-3	ovarian:	n/a
23	chr12:11549192-11549242	HCM	heart:	n/a
24	chr12:11509583-11509633	BJ	skin:	n/a
25	chr12:11549192-11549242	AG04450	lung:	fetal
26	chr12:11549192-11549242	GM06990	blood:	n/a
27	chr12:11508049-11508099	HEEpiC	esophagus:	n/a
28	chr12:11508049-11508099	H1-hESC	embryonic stem cell:	embryo
29	chr12:11548867-11548917	PrEC	prostate:	n/a
30	chr12:11549555-11549605	SK-N-SH	brain:	n/a
31	chr12:11549192-11549242	ProgFib	skin:	n/a
32	chr12:11548867-11548917	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:11548019-11548069	AG09309	skin:	n/a
34	chr12:11548019-11548069	HNPCEpiC	eye:	n/a
35	chr12:11509583-11509633	HNPCEpiC	eye:	n/a
36	chr12:11549555-11549605	Hela-S3	cervix:	n/a
37	chr12:11508049-11508099	GM12878	blood:	n/a
38	chr12:11549192-11549242	HEK293	kidney:	embryo
39	chr12:11548867-11548917	LNCaP	prostate:	n/a
40	chr12:11549555-11549605	GM12891	blood:	n/a
41	chr12:11508049-11508099	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:11549555-11549605	LNCaP	prostate:	n/a
43	chr12:11549555-11549605	HRE	kidney:	n/a
44	chr12:11548019-11548069	HUVEC	blood vessel:	n/a
45	chr12:11548019-11548069	AG04450	lung:	fetal
46	chr12:11549555-11549605	NHDF-neo	bronchial:	n/a
47	chr12:11548867-11548917	SK-N-MC	brain:	n/a
48	chr12:11549555-11549605	AG10803	skin:	n/a
49	chr12:11548867-11548917	GM12892	blood:	n/a
50	chr12:11549555-11549605	AG09309	skin:	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:4 , 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	chr12:11559632-11559826	ENSG00000255790.1
3	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
4	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: 3445 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3445 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9971667	chr12:11493164-11493165	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544008429	chr12:11493174-11493175	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs79373620	chr12:11493188-11493189	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs78524412	chr12:11493210-11493211	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552586381	chr12:11493211-11493212	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138423774	chr12:11493215-11493216	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560755437	chr12:11493227-11493228	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142799720	chr12:11493236-11493237	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567992963	chr12:11493245-11493246	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs202013348	chr12:11493305-11493306	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376616689	chr12:11493306-11493307	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555854778	chr12:11493314-11493315	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190419176	chr12:11493372-11493373	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147417031	chr12:11493429-11493430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182670096	chr12:11493462-11493463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539165255	chr12:11493497-11493498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs56957757	chr12:11493501-11493502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572893430	chr12:11493510-11493511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535415587	chr12:11493521-11493522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555328468	chr12:11493528-11493529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575168428	chr12:11493534-11493535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs118182813	chr12:11493641-11493642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563725006	chr12:11493673-11493674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185425427	chr12:11493685-11493686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529686948	chr12:11493817-11493818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545990668	chr12:11493826-11493827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149538238	chr12:11493833-11493834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189788760	chr12:11493851-11493852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182439691	chr12:11493878-11493879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561688124	chr12:11493880-11493881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537632340	chr12:11493881-11493882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557964891	chr12:11493888-11493889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114489746	chr12:11493943-11493944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12820508	chr12:11493963-11493964	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs570566614	chr12:11493968-11493969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539586497	chr12:11493982-11493983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546401579	chr12:11493992-11493993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1816223	chr12:11494021-11494022	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs371069236	chr12:11494058-11494059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540107471	chr12:11494064-11494065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535475055	chr12:11494086-11494087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553665299	chr12:11494113-11494114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374143119	chr12:11494173-11494174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116225124	chr12:11494196-11494197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1834860	chr12:11494222-11494223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557591114	chr12:11494223-11494224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577381179	chr12:11494253-11494254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202158749	chr12:11494265-11494266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200321264	chr12:11494267-11494268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35976233	chr12:11494268-11494269	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:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:11497200-11497800	Enhancers	HepG2	liver
8	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
9	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel
11	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
12	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
16	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
17	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
19	chr12:11513000-11513800	Enhancers	HMEC	breast
20	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr12:11513000-11514000	Enhancers	NHEK	skin
22	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:11516600-11517000	Enhancers	HepG2	liver
26	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
37	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
38	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr12:11550000-11550600	Enhancers	HUVEC	blood vessel
40	chr12:11550000-11550800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:11550000-11551000	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr12:11550200-11550800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr12:11550200-11550800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr12:11550200-11551000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr12:11550800-11551600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr12:11550800-11568400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:11551600-11551800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr12:11560600-11561800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:11561000-11561600	Enhancers	HMEC	breast
50	chr12:11561000-11561800	Enhancers	NHEK	skin

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