Variant report

Variant	esv2762979
Chromosome Location	chr12:50719438-50736171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:145)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:145 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:50719928-50720204	HepG2	liver:	n/a	n/a
2	ATF3	chr12:50735830-50736079	K562	blood:	n/a	n/a
3	CEBPB	chr12:50720374-50720944	A549	lung:	n/a	n/a
4	CEBPB	chr12:50720517-50720730	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:50719555-50720077	A549	lung:	n/a	chr12:50719728-50719739
6	CEBPB	chr12:50720433-50720841	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:50719564-50720198	MCF-7	breast:	n/a	chr12:50719728-50719739
8	CEBPB	chr12:50720470-50720803	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:50720399-50720913	MCF-7	breast:	n/a	n/a
10	CEBPB	chr12:50719566-50719966	A549	lung:	n/a	chr12:50719728-50719739
11	CEBPB	chr12:50719711-50719826	K562	blood:	n/a	chr12:50719728-50719739
12	CEBPB	chr12:50719545-50720275	A549	lung:	n/a	chr12:50719728-50719739
13	CEBPB	chr12:50720417-50720872	A549	lung:	n/a	n/a
14	CEBPB	chr12:50719562-50719898	IMR90	lung:	n/a	chr12:50719728-50719739
15	CEBPB	chr12:50719616-50720083	HepG2	liver:	n/a	chr12:50719728-50719739
16	CEBPB	chr12:50719542-50720113	Hela-S3	cervix:	n/a	chr12:50719728-50719739
17	CEBPB	chr12:50733572-50733709	K562	blood:	n/a	n/a
18	CEBPB	chr12:50720355-50720822	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:50720474-50720797	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:50720439-50720957	A549	lung:	n/a	n/a
21	CEBPB	chr12:50733616-50733650	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:50735932-50736109	K562	blood:	n/a	n/a
23	CHD2	chr12:50720556-50720660	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:50720680-50720830	AG09319	gingival:	n/a	n/a
25	CTCF	chr12:50720680-50720830	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr12:50720580-50720730	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr12:50720720-50720870	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr12:50720680-50720830	A549	lung:	n/a	n/a
29	CTCF	chr12:50720680-50720830	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr12:50724093-50724256	GM12878	blood:	n/a	chr12:50724142-50724163
31	CTCF	chr12:50720620-50720770	SAEC	small airway:	n/a	n/a
32	CTCF	chr12:50720700-50720850	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr12:50720694-50720765	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr12:50720640-50720790	HMF	breast:	n/a	n/a
35	CTCF	chr12:50720680-50720830	BJ	skin:	n/a	n/a
36	CTCF	chr12:50720660-50720810	HPF	lung:	n/a	n/a
37	CTCF	chr12:50720680-50720830	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr12:50720680-50720830	HMF	breast:	n/a	n/a
39	CTCF	chr12:50731740-50731890	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:50720740-50720890	AG09309	skin:	n/a	n/a
41	CTCF	chr12:50720680-50720830	AG10803	skin:	n/a	n/a
42	CTCF	chr12:50720700-50720850	HPF	lung:	n/a	n/a
43	CTCF	chr12:50720740-50720890	HMEC	breast:	n/a	n/a
44	CTCF	chr12:50720460-50720610	HCM	heart:	n/a	n/a
45	CTCF	chr12:50720740-50720890	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr12:50720640-50720790	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr12:50724109-50724209	HUVEC	blood vessel:	n/a	chr12:50724142-50724163
48	CTCF	chr12:50720708-50720767	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:50720680-50720830	HCFaa	heart:	n/a	n/a
50	CTCF	chr12:50720600-50720750	AoAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50720139-50720189	HIPEpiC	eye:	n/a
2	chr12:50720139-50720189	K562	blood:	n/a
3	chr12:50720139-50720189	SK-N-SH_RA	brain:	n/a
4	chr12:50720139-50720189	SK-N-MC	brain:	n/a
5	chr12:50720139-50720189	AG10803	skin:	n/a
6	chr12:50720139-50720189	SKMC	muscle:	n/a
7	chr12:50720139-50720189	RPTEC	kidney:	n/a
8	chr12:50720139-50720189	Caco-2	colon:	n/a
9	chr12:50720139-50720189	HCPEpiC	choroid plexus:	n/a
10	chr12:50720139-50720189	HRE	kidney:	n/a
11	chr12:50720139-50720189	HRCEpiC	kidney:	n/a
12	chr12:50720139-50720189	AG04450	lung:	fetal
13	chr12:50720139-50720189	NHDF-neo	bronchial:	n/a
14	chr12:50720139-50720189	IMR90	lung:	fetal
15	chr12:50720139-50720189	AG04449	skin:	fetal
16	chr12:50720139-50720189	GM12878	blood:	n/a
17	chr12:50720139-50720189	GM12891	blood:	n/a
18	chr12:50720139-50720189	HMEC	breast:	n/a
19	chr12:50720139-50720189	AG09309	skin:	n/a
20	chr12:50720139-50720189	ECC-1	luminal epithelium:	n/a
21	chr12:50720139-50720189	SK-N-SH	brain:	n/a
22	chr12:50720139-50720189	HCF	heart:	n/a
23	chr12:50720139-50720189	AoSMC	blood vessel:	n/a
24	chr12:50720139-50720189	HCM	heart:	n/a
25	chr12:50720139-50720189	ovcar-3	ovarian:	n/a
26	chr12:50720139-50720189	T-47D	breast:	n/a
27	chr12:50720139-50720189	PrEC	prostate:	n/a
28	chr12:50720139-50720189	MCF10A-Er-Src	breast:	n/a
29	chr12:50720139-50720189	A549	lung:	n/a
30	chr12:50720139-50720189	NB4	blood:	n/a
31	chr12:50720139-50720189	LNCaP	prostate:	n/a
32	chr12:50720139-50720189	CMK	blood:	n/a
33	chr12:50720139-50720189	PANC-1	pancreas:	n/a
34	chr12:50720139-50720189	AG09319	gingival:	n/a
35	chr12:50720139-50720189	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:50720139-50720189	MCF-7	breast:	n/a
37	chr12:50720139-50720189	HAEpiC	amniotic membrane:	n/a
38	chr12:50720139-50720189	HepG2	liver:	n/a
39	chr12:50720139-50720189	HRPEpiC	eye:	n/a
40	chr12:50720139-50720189	HCT-116	colon:	n/a
41	chr12:50720139-50720189	GM06990	blood:	n/a
42	chr12:50720139-50720189	GM12892	blood:	n/a
43	chr12:50720139-50720189	NH-A	brain:	n/a
44	chr12:50720139-50720189	HUVEC	blood vessel:	n/a
45	chr12:50720139-50720189	Hepatocyte	liver:	n/a
46	chr12:50720139-50720189	BJ	skin:	n/a
47	chr12:50720139-50720189	NT2-D1	testis:	n/a
48	chr12:50720139-50720189	HL-60	blood:	n/a
49	chr12:50720139-50720189	HNPCEpiC	eye:	n/a
50	chr12:50720139-50720189	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr12:50728708..50730581-chr12:50746052..50748839,2	K562	blood:
2	chr12:50730126..50732365-chr17:57921759..57924342,2	MCF-7	breast:
3	chr12:50720749..50723312-chr12:50808337..50810670,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM186A	TF binding region
FAM186A	CpG island

Extended variants
information (count: 289 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565673164	chr12:50719445-50719446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528105642	chr12:50719532-50719533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551659015	chr12:50719534-50719535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74941968	chr12:50719556-50719557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537216344	chr12:50719601-50719602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150865877	chr12:50719652-50719653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115859691	chr12:50719670-50719671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183282181	chr12:50719772-50719773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555450103	chr12:50719832-50719833	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs74090103	chr12:50719839-50719840	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112776999	chr12:50719869-50719870	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs568615698	chr12:50719909-50719910	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs547995543	chr12:50719913-50719914	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs557992931	chr12:50719916-50719917	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs192216038	chr12:50719920-50719921	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs544120649	chr12:50719965-50719966	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs563726754	chr12:50720006-50720007	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35391747	chr12:50720008-50720009	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375652521	chr12:50720020-50720021	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542706377	chr12:50720052-50720053	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368246504	chr12:50720147-50720148	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115546976	chr12:50720180-50720181	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537596526	chr12:50720231-50720232	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184461498	chr12:50720268-50720269	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11169380	chr12:50720308-50720309	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116753940	chr12:50720321-50720322	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149625396	chr12:50720348-50720349	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187993014	chr12:50720367-50720368	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34098872	chr12:50720373-50720374	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567306950	chr12:50720374-50720375	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141950669	chr12:50720388-50720389	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79402824	chr12:50720390-50720391	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536449256	chr12:50720416-50720417	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193248590	chr12:50720438-50720439	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11169381	chr12:50720460-50720461	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565851444	chr12:50720544-50720545	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534823653	chr12:50720571-50720572	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184504703	chr12:50720611-50720612	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114715017	chr12:50720639-50720640	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189478735	chr12:50720687-50720688	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147321970	chr12:50720708-50720709	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574106802	chr12:50720722-50720723	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543267795	chr12:50720731-50720732	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559456600	chr12:50720813-50720814	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572960175	chr12:50720866-50720867	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536044247	chr12:50720870-50720871	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141049869	chr12:50720872-50720873	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144592004	chr12:50720964-50720965	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550553519	chr12:50720971-50720972	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375183954	chr12:50720984-50720985	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50692000-50719800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:50693600-50722800	Weak transcription	Fetal Intestine Small	intestine
3	chr12:50706400-50720000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:50707400-50720000	Weak transcription	Osteobl	bone
5	chr12:50707400-50720400	Weak transcription	Stomach Mucosa	stomach
6	chr12:50707600-50719600	Weak transcription	A549	lung
7	chr12:50709800-50719800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr12:50716200-50719600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr12:50716200-50720000	Weak transcription	Fetal Lung	lung
10	chr12:50717600-50719800	Enhancers	Liver	Liver
11	chr12:50717800-50720400	Weak transcription	Brain Angular Gyrus	brain
12	chr12:50718000-50719800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:50718600-50719600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:50719400-50719800	Enhancers	Ovary	ovary
15	chr12:50719400-50720000	Enhancers	Hela-S3	cervix
16	chr12:50719400-50720400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:50719600-50719800	Enhancers	A549	lung
18	chr12:50719600-50720200	Enhancers	Duodenum Mucosa	Duodenum
19	chr12:50719600-50721600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr12:50719800-50720000	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr12:50719800-50720400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:50719800-50720600	Flanking Active TSS	Liver	Liver
23	chr12:50719800-50720600	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr12:50719800-50721000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:50719800-50721000	Enhancers	Adipose Nuclei	Adipose
26	chr12:50719800-50721000	Enhancers	Colonic Mucosa	Colon
27	chr12:50719800-50721000	Enhancers	Fetal Intestine Large	intestine
28	chr12:50719800-50721000	Enhancers	Pancreas	Pancrea
29	chr12:50719800-50721000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr12:50719800-50721000	Enhancers	HepG2	liver
31	chr12:50719800-50721200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr12:50719800-50721200	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:50719800-50721200	Flanking Active TSS	A549	lung
34	chr12:50719800-50721400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr12:50719800-50721600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:50720000-50720200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr12:50720000-50720200	Enhancers	Esophagus	oesophagus
38	chr12:50720000-50720200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr12:50720000-50720400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr12:50720000-50720400	Enhancers	Osteobl	bone
41	chr12:50720000-50720600	Enhancers	Aorta	Aorta
42	chr12:50720000-50720800	Enhancers	Fetal Lung	lung
43	chr12:50720000-50720800	Flanking Active TSS	Hela-S3	cervix
44	chr12:50720000-50721200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:50720200-50720400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:50720200-50721000	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr12:50720200-50721200	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr12:50720400-50720600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:50720400-50720600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:50720400-50720600	Enhancers	Brain Angular Gyrus	brain

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