Variant report

Variant	nsv900580
Chromosome Location	chr13:76665408-76735400
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	ATF1	chr13:76711905-76712094	K562	blood:	n/a	n/a
2	CCNT2	chr13:76673714-76673907	K562	blood:	n/a	n/a
3	CEBPB	chr13:76716118-76716181	H1-hESC	embryonic stem cell:	n/a	chr13:76716142-76716153
4	CEBPB	chr13:76698248-76698479	HepG2	liver:	n/a	chr13:76698389-76698400
5	CEBPB	chr13:76728261-76728550	A549	lung:	n/a	chr13:76728401-76728412 chr13:76728402-76728413 chr13:76728401-76728414
6	CEBPB	chr13:76723131-76723544	IMR90	lung:	n/a	n/a
7	CEBPB	chr13:76728237-76728552	IMR90	lung:	n/a	chr13:76728401-76728412 chr13:76728402-76728413 chr13:76728401-76728414
8	CEBPB	chr13:76674706-76674865	IMR90	lung:	n/a	n/a
9	CEBPB	chr13:76728249-76728559	HepG2	liver:	n/a	chr13:76728401-76728412 chr13:76728402-76728413 chr13:76728401-76728414
10	CEBPB	chr13:76715973-76716300	HepG2	liver:	n/a	chr13:76716142-76716153
11	CEBPB	chr13:76698249-76698539	A549	lung:	n/a	chr13:76698389-76698400
12	CEBPB	chr13:76715978-76716283	IMR90	lung:	n/a	chr13:76716142-76716153
13	CEBPB	chr13:76715983-76716242	K562	blood:	n/a	chr13:76716142-76716153
14	CEBPB	chr13:76715980-76716246	A549	lung:	n/a	chr13:76716142-76716153
15	CEBPB	chr13:76698216-76698579	IMR90	lung:	n/a	chr13:76698389-76698400
16	CTCF	chr13:76692273-76692353	GM20000	blood:	n/a	n/a
17	CTCF	chr13:76711240-76711390	NHLF	lung:	n/a	n/a
18	CTCF	chr13:76705876-76705946	GM20000	blood:	n/a	n/a
19	CTCF	chr13:76694958-76694999	Kidney_OC	kidney:	n/a	n/a
20	E2F4	chr13:76694339-76694539	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr13:76717265-76717424	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr13:76731686-76731773	K562	blood:	n/a	n/a
23	FOS	chr13:76723236-76723335	MCF10A-Er-Src	breast:	n/a	n/a
24	FOSL2	chr13:76722973-76723515	SK-N-SH	brain:	n/a	n/a
25	GATA2	chr13:76682806-76683287	SH-SY5Y	brain:	n/a	chr13:76683121-76683129
26	GATA3	chr13:76683007-76683256	SH-SY5Y	brain:	n/a	chr13:76683121-76683129
27	GATA3	chr13:76679760-76680106	SH-SY5Y	brain:	n/a	chr13:76679805-76679814
28	JUN	chr13:76698329-76698518	HepG2	liver:	n/a	chr13:76698386-76698399
29	JUND	chr13:76723038-76723462	SK-N-SH	brain:	n/a	n/a
30	KAP1	chr13:76697676-76698275	HEK293	kidney:	n/a	n/a
31	KAP1	chr13:76698516-76698772	HEK293	kidney:	n/a	n/a
32	MAFF	chr13:76681685-76681873	HepG2	liver:	n/a	chr13:76681814-76681832
33	MAFF	chr13:76717352-76717513	HepG2	liver:	n/a	n/a
34	MAFK	chr13:76717281-76717583	HepG2	liver:	n/a	chr13:76717429-76717444 chr13:76717429-76717445 chr13:76717425-76717442
35	MAFK	chr13:76681709-76681950	HepG2	liver:	n/a	n/a
36	MAFK	chr13:76704391-76704637	HepG2	liver:	n/a	n/a
37	MAFK	chr13:76705688-76705824	HepG2	liver:	n/a	n/a
38	MAFK	chr13:76717313-76717579	IMR90	lung:	n/a	chr13:76717429-76717444 chr13:76717429-76717445 chr13:76717425-76717442
39	MAFK	chr13:76714346-76714561	HepG2	liver:	n/a	n/a
40	MAFK	chr13:76681769-76681853	HepG2	liver:	n/a	n/a
41	MAFK	chr13:76717387-76717548	HepG2	liver:	n/a	chr13:76717429-76717444 chr13:76717429-76717445 chr13:76717425-76717442
42	MAFK	chr13:76674187-76674371	HepG2	liver:	n/a	n/a
43	MAFK	chr13:76704453-76704596	HepG2	liver:	n/a	n/a
44	MAFK	chr13:76718501-76718628	HepG2	liver:	n/a	n/a
45	MAX	chr13:76702049-76702080	HepG2	liver:	n/a	n/a
46	MAZ	chr13:76730110-76730200	HepG2	liver:	n/a	n/a
47	MAZ	chr13:76722867-76723518	IMR90	lung:	n/a	n/a
48	MYC	chr13:76719815-76719901	GM12878	blood:	n/a	n/a
49	MYC	chr13:76725348-76725447	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr13:76732064-76732458	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76723380-76723430	NHDF-neo	bronchial:	n/a
2	chr13:76723380-76723430	BE2_C	brain:	n/a
3	chr13:76723380-76723430	GM12878	blood:	n/a
4	chr13:76723380-76723430	LNCaP	prostate:	n/a
5	chr13:76723380-76723430	A549	lung:	n/a
6	chr13:76723380-76723430	SK-N-MC	brain:	n/a
7	chr13:76723380-76723430	HIPEpiC	eye:	n/a
8	chr13:76723380-76723430	AG10803	skin:	n/a
9	chr13:76723380-76723430	SK-N-SH	brain:	n/a
10	chr13:76723380-76723430	Hela-S3	cervix:	n/a
11	chr13:76723380-76723430	HPAEpiC	pulmonary alveolar:	n/a
12	chr13:76723380-76723430	ovcar-3	ovarian:	n/a
13	chr13:76723380-76723430	MCF10A-Er-Src	breast:	n/a
14	chr13:76723380-76723430	HCPEpiC	choroid plexus:	n/a
15	chr13:76723380-76723430	PANC-1	pancreas:	n/a
16	chr13:76723380-76723430	HL-60	blood:	n/a
17	chr13:76723380-76723430	HEEpiC	esophagus:	n/a
18	chr13:76723380-76723430	K562	blood:	n/a
19	chr13:76723380-76723430	RPTEC	kidney:	n/a
20	chr13:76723380-76723430	AG09309	skin:	n/a
21	chr13:76723380-76723430	HRE	kidney:	n/a
22	chr13:76723380-76723430	HEK293	kidney:	embryo
23	chr13:76723380-76723430	AG04450	lung:	fetal
24	chr13:76723380-76723430	AG09319	gingival:	n/a
25	chr13:76723380-76723430	GM06990	blood:	n/a
26	chr13:76723380-76723430	NHBE	bronchial:	n/a
27	chr13:76723380-76723430	Jurkat	blood:	n/a
28	chr13:76723380-76723430	ProgFib	skin:	n/a
29	chr13:76723380-76723430	SAEC	small airway:	n/a
30	chr13:76723380-76723430	CMK	blood:	n/a
31	chr13:76723380-76723430	GM12891	blood:	n/a
32	chr13:76723380-76723430	AG04449	skin:	fetal
33	chr13:76723380-76723430	Caco-2	colon:	n/a
34	chr13:76723380-76723430	NH-A	brain:	n/a
35	chr13:76723380-76723430	SK-N-SH_RA	brain:	n/a
36	chr13:76723380-76723430	HCM	heart:	n/a
37	chr13:76723380-76723430	IMR90	lung:	fetal
38	chr13:76723380-76723430	HAEpiC	amniotic membrane:	n/a
39	chr13:76723380-76723430	PrEC	prostate:	n/a
40	chr13:76723380-76723430	T-47D	breast:	n/a
41	chr13:76723380-76723430	HRCEpiC	kidney:	n/a
42	chr13:76723380-76723430	HepG2	liver:	n/a
43	chr13:76723380-76723430	Hepatocyte	liver:	n/a
44	chr13:76723380-76723430	BJ	skin:	n/a
45	chr13:76723380-76723430	HUVEC	blood vessel:	n/a
46	chr13:76723380-76723430	H1-hESC	embryonic stem cell:	embryo
47	chr13:76723380-76723430	MCF-7	breast:	n/a
48	chr13:76723380-76723430	GM19239	blood:	n/a
49	chr13:76723380-76723430	HCT-116	colon:	n/a
50	chr13:76723380-76723430	NB4	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL359392.1-5	chr13:76709067-76709360	NONHSAT034379

Variant related genes	Relation type
RN7SL571P	TF binding region
RN7SL571P	CpG island

Extended variants
information (count: 1463 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1463 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184521928	chr13:76669853-76669854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540226986	chr13:76669856-76669857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555689067	chr13:76669883-76669884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9544154	chr13:76669885-76669886	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544438911	chr13:76669899-76669900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563110438	chr13:76669908-76669909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115407169	chr13:76669941-76669942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374222027	chr13:76669954-76669955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190484558	chr13:76669973-76669974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558570219	chr13:76670006-76670007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545088270	chr13:76670007-76670008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559948288	chr13:76670008-76670009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527322496	chr13:76670023-76670024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148581068	chr13:76670035-76670036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567593586	chr13:76670050-76670051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531620670	chr13:76670080-76670081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575210320	chr13:76670094-76670095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538246693	chr13:76670102-76670103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556342206	chr13:76670109-76670110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571423243	chr13:76670124-76670125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12877102	chr13:76670140-76670141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558274317	chr13:76670141-76670142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142369500	chr13:76670153-76670154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371290235	chr13:76670154-76670155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7324382	chr13:76670162-76670163	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191774698	chr13:76686482-76686483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs369341491	chr13:76686513-76686514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs550851935	chr13:76686536-76686537	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs2663230	chr13:76686541-76686542	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539638390	chr13:76686551-76686552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs181629245	chr13:76686554-76686555	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs570839451	chr13:76686578-76686579	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs531347240	chr13:76686596-76686597	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs535080735	chr13:76686602-76686603	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs534443963	chr13:76686607-76686608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs574732735	chr13:76686635-76686636	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs185461270	chr13:76686642-76686643	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557224239	chr13:76686668-76686669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs190266911	chr13:76686777-76686778	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs545967613	chr13:76686821-76686822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564242362	chr13:76686822-76686823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4885382	chr13:76686823-76686824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572868212	chr13:76686824-76686825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60815888	chr13:76686843-76686844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141867788	chr13:76686844-76686845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79168911	chr13:76686874-76686875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149466618	chr13:76686892-76686893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528871525	chr13:76686893-76686894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550937914	chr13:76686903-76686904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143868491	chr13:76686927-76686928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76669800-76670200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr13:76686400-76686800	ZNF genes & repeats	Aorta	Aorta
3	chr13:76686800-76691600	Weak transcription	Aorta	Aorta
4	chr13:76690400-76691600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr13:76691600-76692600	ZNF genes & repeats	Aorta	Aorta
6	chr13:76692200-76692400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:76692400-76694800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr13:76692600-76697400	Weak transcription	Aorta	Aorta
9	chr13:76697400-76697600	ZNF genes & repeats	Aorta	Aorta
10	chr13:76697400-76698800	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr13:76703000-76703200	Enhancers	Psoas Muscle	Psoas
12	chr13:76703200-76704000	Enhancers	Fetal Heart	heart
13	chr13:76703200-76704000	Enhancers	HSMMtube	muscle
14	chr13:76703400-76704000	Enhancers	Fetal Lung	lung
15	chr13:76703400-76704000	Enhancers	Right Atrium	heart
16	chr13:76703600-76704000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr13:76703600-76704600	Enhancers	Fetal Muscle Leg	muscle
18	chr13:76704000-76705800	Weak transcription	Fetal Heart	heart
19	chr13:76704000-76705800	Weak transcription	Fetal Lung	lung
20	chr13:76705800-76706200	Enhancers	Fetal Brain Male	brain
21	chr13:76705800-76706200	Enhancers	Fetal Lung	lung
22	chr13:76705800-76706400	Enhancers	Fetal Heart	heart
23	chr13:76706400-76706800	Weak transcription	Fetal Heart	heart
24	chr13:76706800-76709400	Enhancers	Fetal Heart	heart
25	chr13:76716200-76717400	Enhancers	Fetal Heart	heart
26	chr13:76722200-76723000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr13:76722400-76723800	Enhancers	HSMM	muscle
28	chr13:76722600-76723200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr13:76722600-76723400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr13:76722600-76723600	Enhancers	NH-A	brain
31	chr13:76722600-76723800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr13:76722600-76723800	Enhancers	HSMMtube	muscle
33	chr13:76722600-76723800	Enhancers	NHLF	lung
34	chr13:76722600-76723800	Enhancers	Osteobl	bone
35	chr13:76722600-76724000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:76722800-76723600	Enhancers	NHDF-Ad	bronchial
37	chr13:76723000-76723400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr13:76723400-76723800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr13:76723800-76724000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr13:76724000-76726400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr13:76726400-76726800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr13:76726800-76728000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:76727600-76727800	Enhancers	Psoas Muscle	Psoas
44	chr13:76727800-76734200	Weak transcription	Psoas Muscle	Psoas
45	chr13:76728200-76728400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr13:76729600-76734200	Weak transcription	Aorta	Aorta
47	chr13:76732000-76732600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr13:76732200-76732400	Enhancers	Fetal Heart	heart
49	chr13:76732200-76732800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr13:76732200-76732800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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