Variant report

Variant	nsv1011
Chromosome Location	chr13:40008962-40034177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr13:40025875-40026305	GM12878	blood:	n/a	n/a
2	BHLHE40	chr13:40024463-40024532	GM12878	blood:	n/a	n/a
3	CEBPB	chr13:40025478-40025817	ECC-1	luminal epithelium:	n/a	chr13:40025610-40025623
4	CEBPB	chr13:40014130-40014496	IMR90	lung:	n/a	chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014311-40014322 chr13:40014312-40014321 chr13:40014310-40014321 chr13:40014310-40014323
5	CEBPB	chr13:40014192-40014421	A549	lung:	n/a	chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014311-40014322 chr13:40014312-40014321 chr13:40014310-40014321 chr13:40014310-40014323
6	CEBPB	chr13:40026159-40026506	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr13:40014146-40014481	HepG2	liver:	n/a	chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014312-40014321 chr13:40014311-40014322 chr13:40014312-40014321 chr13:40014310-40014321 chr13:40014310-40014323
8	CEBPB	chr13:40025399-40025784	ECC-1	luminal epithelium:	n/a	chr13:40025610-40025623
9	CEBPB	chr13:40025549-40025662	A549	lung:	n/a	chr13:40025610-40025623
10	E2F4	chr13:40016268-40016468	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr13:40024443-40024539	GM12878	blood:	n/a	n/a
12	EP300	chr13:40026102-40026122	GM12878	blood:	n/a	n/a
13	EP300	chr13:40029699-40029962	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr13:40025996-40026196	GM12878	blood:	n/a	chr13:40026035-40026049
15	EP300	chr13:40029759-40029960	SK-N-SH_RA	brain:	n/a	n/a
16	FOS	chr13:40025574-40025632	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXP2	chr13:40026251-40026374	PFSK-1	brain:	n/a	n/a
18	GATA1	chr13:40018813-40019481	PBDE	blood:	n/a	n/a
19	GATA1	chr13:40019966-40021254	PBDE	blood:	n/a	chr13:40020023-40020033 chr13:40020306-40020323 chr13:40020395-40020404
20	GATA2	chr13:40029789-40030389	HUVEC	blood vessel:	n/a	chr13:40030130-40030147 chr13:40029843-40029850 chr13:40030136-40030152 chr13:40030134-40030155
21	GATA2	chr13:40026970-40027225	SH-SY5Y	brain:	n/a	chr13:40027079-40027087
22	GATA2	chr13:40029652-40030459	SH-SY5Y	brain:	n/a	chr13:40030130-40030147 chr13:40029843-40029850 chr13:40030136-40030152 chr13:40030134-40030155
23	GATA2	chr13:40021561-40021893	SH-SY5Y	brain:	n/a	chr13:40021684-40021705
24	GATA3	chr13:40029413-40030551	SH-SY5Y	brain:	n/a	chr13:40030130-40030147 chr13:40029843-40029850 chr13:40030136-40030152 chr13:40030134-40030155 chr13:40029462-40029473
25	GATA3	chr13:40021561-40021748	SH-SY5Y	brain:	n/a	chr13:40021684-40021705
26	GATA3	chr13:40026820-40027097	SH-SY5Y	brain:	n/a	chr13:40027079-40027087
27	GATA3	chr13:40029990-40030305	T-47D	breast:	n/a	chr13:40030130-40030147 chr13:40030136-40030152 chr13:40030134-40030155
28	GATA3	chr13:40029670-40030387	SK-N-SH	brain:	n/a	chr13:40030130-40030147 chr13:40029843-40029850 chr13:40030136-40030152 chr13:40030134-40030155
29	KAP1	chr13:40012609-40012989	HEK293	kidney:	n/a	n/a
30	KAP1	chr13:40025670-40026999	HEK293	kidney:	n/a	chr13:40026171-40026179
31	KAP1	chr13:40029863-40030263	U2OS	brain:	n/a	n/a
32	KAP1	chr13:40025874-40026399	U2OS	brain:	n/a	chr13:40026171-40026179
33	MAFK	chr13:40033612-40033841	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAFK	chr13:40033498-40033823	IMR90	lung:	n/a	n/a
35	MAFK	chr13:40031410-40031749	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr13:40025907-40026934	NB4	blood:	n/a	n/a
37	MAX	chr13:40025199-40025262	NB4	blood:	n/a	n/a
38	MEF2A	chr13:40025928-40026351	GM12878	blood:	n/a	chr13:40026114-40026128 chr13:40026112-40026133 chr13:40026112-40026133
39	MEF2A	chr13:40025968-40026275	GM12878	blood:	n/a	chr13:40026114-40026128 chr13:40026112-40026133 chr13:40026112-40026133
40	MEF2C	chr13:40025812-40026313	GM12878	blood:	n/a	chr13:40026114-40026128 chr13:40026112-40026133 chr13:40026112-40026133
41	MXI1	chr13:40019930-40019985	GM12878	blood:	n/a	n/a
42	MYC	chr13:40025465-40027107	NB4	blood:	n/a	n/a
43	NFIC	chr13:40025366-40025911	SK-N-SH	brain:	n/a	chr13:40025592-40025608 chr13:40025592-40025609 chr13:40025594-40025610
44	NFIC	chr13:40025331-40025951	ECC-1	luminal epithelium:	n/a	chr13:40025592-40025608 chr13:40025592-40025609 chr13:40025594-40025610
45	NFIC	chr13:40025417-40025897	ECC-1	luminal epithelium:	n/a	chr13:40025592-40025608 chr13:40025592-40025609 chr13:40025594-40025610
46	POLR2A	chr13:40030248-40030353	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr13:40025833-40026604	HL-60	blood:	n/a	n/a
48	POLR2A	chr13:40024420-40024422	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr13:40025832-40026467	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr13:40026116-40026556	HL-60	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:40028098-40028148	PrEC	prostate:	n/a
2	chr13:40028098-40028148	H1-hESC	embryonic stem cell:	embryo
3	chr13:40026426-40026476	AG09309	skin:	n/a
4	chr13:40028098-40028148	HL-60	blood:	n/a
5	chr13:40028098-40028148	NB4	blood:	n/a
6	chr13:40028098-40028148	HEK293	kidney:	embryo
7	chr13:40028098-40028148	HCT-116	colon:	n/a
8	chr13:40026426-40026476	BJ	skin:	n/a
9	chr13:40026426-40026476	NHBE	bronchial:	n/a
10	chr13:40026426-40026476	HMEC	breast:	n/a
11	chr13:40028098-40028148	K562	blood:	n/a
12	chr13:40028098-40028148	AG09309	skin:	n/a
13	chr13:40026426-40026476	HNPCEpiC	eye:	n/a
14	chr13:40028098-40028148	T-47D	breast:	n/a
15	chr13:40028098-40028148	HEEpiC	esophagus:	n/a
16	chr13:40026426-40026476	K562	blood:	n/a
17	chr13:40028098-40028148	HMEC	breast:	n/a
18	chr13:40026426-40026476	NT2-D1	testis:	n/a
19	chr13:40026426-40026476	LNCaP	prostate:	n/a
20	chr13:40028098-40028148	HNPCEpiC	eye:	n/a
21	chr13:40028098-40028148	ovcar-3	ovarian:	n/a
22	chr13:40026426-40026476	HIPEpiC	eye:	n/a
23	chr13:40028098-40028148	NHBE	bronchial:	n/a
24	chr13:40026426-40026476	SKMC	muscle:	n/a
25	chr13:40028098-40028148	PANC-1	pancreas:	n/a
26	chr13:40026426-40026476	PANC-1	pancreas:	n/a
27	chr13:40028098-40028148	ECC-1	luminal epithelium:	n/a
28	chr13:40028098-40028148	BJ	skin:	n/a
29	chr13:40028098-40028148	A549	lung:	n/a
30	chr13:40026426-40026476	HRCEpiC	kidney:	n/a
31	chr13:40028098-40028148	MCF-7	breast:	n/a
32	chr13:40026426-40026476	HCPEpiC	choroid plexus:	n/a
33	chr13:40026426-40026476	GM12878	blood:	n/a
34	chr13:40028098-40028148	AG04450	lung:	fetal
35	chr13:40026426-40026476	HEK293	kidney:	embryo
36	chr13:40028098-40028148	PFSK-1	brain:	n/a
37	chr13:40028098-40028148	IMR90	lung:	fetal
38	chr13:40028098-40028148	Caco-2	colon:	n/a
39	chr13:40026426-40026476	HEEpiC	esophagus:	n/a
40	chr13:40026426-40026476	GM12891	blood:	n/a
41	chr13:40026426-40026476	Hela-S3	cervix:	n/a
42	chr13:40026426-40026476	HPAEpiC	pulmonary alveolar:	n/a
43	chr13:40026426-40026476	U87	brain:	n/a
44	chr13:40026426-40026476	GM06990	blood:	n/a
45	chr13:40026426-40026476	AG04450	lung:	fetal
46	chr13:40026426-40026476	CMK	blood:	n/a
47	chr13:40026426-40026476	HAEpiC	amniotic membrane:	n/a
48	chr13:40028098-40028148	RPTEC	kidney:	n/a
49	chr13:40026426-40026476	H1-hESC	embryonic stem cell:	embryo
50	chr13:40026426-40026476	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:40016286..40017209-chr6:84924987..84925612,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238408	TF binding region
ENSG00000238408	CpG island

Extended variants
information (count: 886 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190174595	chr13:40008965-40008966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111858814	chr13:40008989-40008990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs57733100	chr13:40008993-40008994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60516718	chr13:40009036-40009037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534845493	chr13:40009054-40009055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554893036	chr13:40009056-40009057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181714263	chr13:40009141-40009142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184533310	chr13:40009149-40009150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189363910	chr13:40009186-40009187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569324568	chr13:40009199-40009200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568409416	chr13:40009211-40009212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55701240	chr13:40009224-40009225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201348496	chr13:40009225-40009226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79744256	chr13:40009227-40009228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528106484	chr13:40009296-40009297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114272891	chr13:40009307-40009308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs499031	chr13:40009393-40009394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537144986	chr13:40009394-40009395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77132438	chr13:40009406-40009407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565702359	chr13:40009408-40009409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73460972	chr13:40009425-40009426	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs180721622	chr13:40009430-40009431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553424797	chr13:40009434-40009435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557333395	chr13:40009435-40009436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573497212	chr13:40009459-40009460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577233615	chr13:40009469-40009470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538936847	chr13:40009515-40009516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372808854	chr13:40009549-40009550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575197222	chr13:40009591-40009592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9548766	chr13:40009626-40009627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561046377	chr13:40009642-40009643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79684810	chr13:40009717-40009718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542789196	chr13:40009782-40009783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553219954	chr13:40009799-40009800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573371282	chr13:40009800-40009801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78097493	chr13:40009822-40009823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542061399	chr13:40009884-40009885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564881559	chr13:40009886-40009887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530508704	chr13:40009946-40009947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550741912	chr13:40009997-40009998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567332120	chr13:40010003-40010004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112439330	chr13:40010008-40010009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547195171	chr13:40010059-40010060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566905548	chr13:40010169-40010170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562043430	chr13:40010175-40010176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538958286	chr13:40010189-40010190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562796974	chr13:40010249-40010250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576832589	chr13:40010251-40010252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145491185	chr13:40010273-40010274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61945315	chr13:40010289-40010290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Monoclonal gammopathy of undetermined significance	19135901	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39992000-40018600	Weak transcription	Right Ventricle	heart
2	chr13:39998000-40022200	Weak transcription	Ovary	ovary
3	chr13:39998200-40012200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr13:40004200-40018600	Weak transcription	Psoas Muscle	Psoas
5	chr13:40004800-40011600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr13:40006800-40012000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:40007000-40012600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:40008000-40009000	Enhancers	Left Ventricle	heart
9	chr13:40011200-40012400	Weak transcription	Lung	lung
10	chr13:40011600-40013800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr13:40012200-40012600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr13:40012400-40013400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
13	chr13:40012600-40013400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:40012600-40015000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:40012800-40013000	Enhancers	Aorta	Aorta
16	chr13:40012800-40013000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
17	chr13:40012800-40013600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
18	chr13:40013000-40016800	Weak transcription	Aorta	Aorta
19	chr13:40013400-40026200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr13:40013800-40023000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:40014600-40015200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr13:40014600-40015200	Enhancers	Left Ventricle	heart
23	chr13:40015000-40023200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr13:40015200-40018600	Weak transcription	Left Ventricle	heart
25	chr13:40015200-40023000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:40015200-40023000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:40016400-40017600	Enhancers	Fetal Heart	heart
28	chr13:40016600-40017800	Enhancers	Right Atrium	heart
29	chr13:40016800-40017000	Enhancers	Aorta	Aorta
30	chr13:40017000-40017400	Weak transcription	Aorta	Aorta
31	chr13:40017400-40017600	Enhancers	Aorta	Aorta
32	chr13:40017600-40019200	Weak transcription	Fetal Heart	heart
33	chr13:40017600-40023000	Weak transcription	Aorta	Aorta
34	chr13:40017600-40026200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr13:40017800-40018800	Weak transcription	Right Atrium	heart
36	chr13:40018600-40019000	Enhancers	Esophagus	oesophagus
37	chr13:40018600-40019000	Enhancers	Gastric	stomach
38	chr13:40018600-40019200	Enhancers	Fetal Muscle Leg	muscle
39	chr13:40018600-40019200	Enhancers	Left Ventricle	heart
40	chr13:40018600-40019200	Enhancers	Lung	lung
41	chr13:40018600-40019200	Enhancers	Psoas Muscle	Psoas
42	chr13:40018600-40019400	Enhancers	Right Ventricle	heart
43	chr13:40018800-40019200	Enhancers	Right Atrium	heart
44	chr13:40019200-40019400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr13:40019200-40020200	Enhancers	Fetal Heart	heart
46	chr13:40019200-40020400	Weak transcription	Left Ventricle	heart
47	chr13:40019200-40020400	Weak transcription	Lung	lung
48	chr13:40019200-40020400	Weak transcription	Right Atrium	heart
49	chr13:40019200-40022000	Weak transcription	Fetal Muscle Leg	muscle
50	chr13:40019200-40023000	Weak transcription	Psoas Muscle	Psoas

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