Variant report

Variant	nsv900384
Chromosome Location	chr13:66289610-66389936
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	CEBPB	chr13:66302696-66303002	IMR90	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
2	CEBPB	chr13:66348740-66349098	HepG2	liver:	n/a	chr13:66348913-66348924
3	CEBPB	chr13:66300708-66300953	IMR90	lung:	n/a	chr13:66300832-66300845
4	CEBPB	chr13:66302788-66302938	A549	lung:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
5	CEBPB	chr13:66357410-66357610	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:66348742-66349098	IMR90	lung:	n/a	chr13:66348913-66348924
7	CEBPB	chr13:66343067-66343334	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:66348781-66349093	A549	lung:	n/a	chr13:66348913-66348924
9	CEBPB	chr13:66367393-66367619	IMR90	lung:	n/a	n/a
10	CEBPB	chr13:66302768-66302924	H1-hESC	embryonic stem cell:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
11	CEBPB	chr13:66302712-66302983	HepG2	liver:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
12	CEBPB	chr13:66343051-66343372	IMR90	lung:	n/a	n/a
13	CEBPB	chr13:66302716-66302972	K562	blood:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
14	CTCF	chr13:66357800-66357950	GM12869	blood:	n/a	n/a
15	CTCF	chr13:66319000-66319150	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr13:66338040-66338190	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr13:66350320-66350470	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr13:66362113-66362146	Medullo	brain:	n/a	n/a
19	CTCF	chr13:66350320-66350470	HMF	breast:	n/a	n/a
20	CTCF	chr13:66350340-66350454	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr13:66350320-66350470	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr13:66350260-66350410	BE2_C	brain:	n/a	n/a
23	CTCF	chr13:66319665-66319688	Fibrobl	skin:	n/a	n/a
24	CTCF	chr13:66338133-66338214	LNCaP	prostate:	n/a	n/a
25	E2F4	chr13:66318652-66318758	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr13:66389749-66390206	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr13:66380583-66380641	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:66310922-66311018	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr13:66382203-66382600	HUVEC	blood vessel:	n/a	n/a
30	FOS	chr13:66300622-66300899	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:66300685-66300886	MCF10A-Er-Src	breast:	n/a	n/a
32	FOXA1	chr13:66336824-66337068	T-47D	breast:	n/a	chr13:66336926-66336941
33	FOXA1	chr13:66336847-66337043	T-47D	breast:	n/a	chr13:66336926-66336941
34	FOXP2	chr13:66298407-66298768	SK-N-MC	brain:	n/a	n/a
35	GATA3	chr13:66289996-66290922	MCF-7	breast:	n/a	chr13:66290452-66290463
36	GATA3	chr13:66385196-66385879	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr13:66318860-66319399	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr13:66380836-66380964	SH-SY5Y	brain:	n/a	chr13:66380878-66380887 chr13:66380878-66380885 chr13:66380878-66380885 chr13:66380877-66380887 chr13:66380874-66380890 chr13:66380871-66380892 chr13:66380887-66380896 chr13:66380878-66380885
39	GATA3	chr13:66385279-66385728	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr13:66326614-66326784	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr13:66290342-66290402	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr13:66290352-66290719	MCF-7	breast:	n/a	chr13:66290452-66290463
43	IKZF1	chr13:66371922-66371996	GM12878	blood:	n/a	n/a
44	JUN	chr13:66328014-66328552	K562	blood:	n/a	n/a
45	JUN	chr13:66382298-66382470	H1-hESC	embryonic stem cell:	n/a	n/a
46	KAP1	chr13:66330183-66330717	HEK293	kidney:	n/a	n/a
47	KAP1	chr13:66386915-66387281	HEK293	kidney:	n/a	n/a
48	KAP1	chr13:66336866-66337218	HEK293	kidney:	n/a	n/a
49	KAP1	chr13:66345966-66346173	U2OS	brain:	n/a	n/a
50	KAP1	chr13:66345812-66346269	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66322551-66322601	MCF10A-Er-Src	breast:	n/a
2	chr13:66322551-66322601	Hepatocyte	liver:	n/a
3	chr13:66322551-66322601	HCF	heart:	n/a
4	chr13:66322551-66322601	SK-N-SH	brain:	n/a
5	chr13:66322551-66322601	BE2_C	brain:	n/a
6	chr13:66322551-66322601	HAEpiC	amniotic membrane:	n/a
7	chr13:66322551-66322601	AG09319	gingival:	n/a
8	chr13:66322551-66322601	GM06990	blood:	n/a
9	chr13:66322551-66322601	NT2-D1	testis:	n/a
10	chr13:66322551-66322601	LNCaP	prostate:	n/a
11	chr13:66322551-66322601	MCF-7	breast:	n/a
12	chr13:66322551-66322601	SK-N-MC	brain:	n/a
13	chr13:66322551-66322601	GM12891	blood:	n/a
14	chr13:66322551-66322601	HRCEpiC	kidney:	n/a
15	chr13:66322551-66322601	NHDF-neo	bronchial:	n/a
16	chr13:66322551-66322601	AG09309	skin:	n/a
17	chr13:66322551-66322601	PFSK-1	brain:	n/a
18	chr13:66322551-66322601	PANC-1	pancreas:	n/a
19	chr13:66322551-66322601	U87	brain:	n/a
20	chr13:66322551-66322601	ECC-1	luminal epithelium:	n/a
21	chr13:66322551-66322601	HNPCEpiC	eye:	n/a
22	chr13:66322551-66322601	NH-A	brain:	n/a
23	chr13:66322551-66322601	A549	lung:	n/a
24	chr13:66322551-66322601	Jurkat	blood:	n/a
25	chr13:66322551-66322601	PrEC	prostate:	n/a
26	chr13:66322551-66322601	GM12878	blood:	n/a
27	chr13:66322551-66322601	BJ	skin:	n/a
28	chr13:66322551-66322601	AoSMC	blood vessel:	n/a
29	chr13:66322551-66322601	HCPEpiC	choroid plexus:	n/a
30	chr13:66322551-66322601	HepG2	liver:	n/a
31	chr13:66322551-66322601	SK-N-SH_RA	brain:	n/a
32	chr13:66322551-66322601	H1-hESC	embryonic stem cell:	embryo
33	chr13:66322551-66322601	RPTEC	kidney:	n/a
34	chr13:66322551-66322601	HL-60	blood:	n/a
35	chr13:66322551-66322601	AG04449	skin:	fetal
36	chr13:66322551-66322601	HCT-116	colon:	n/a
37	chr13:66322551-66322601	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:66322551-66322601	SKMC	muscle:	n/a
39	chr13:66322551-66322601	CMK	blood:	n/a
40	chr13:66322551-66322601	ovcar-3	ovarian:	n/a
41	chr13:66322551-66322601	IMR90	lung:	fetal
42	chr13:66322551-66322601	HEK293	kidney:	embryo
43	chr13:66322551-66322601	NB4	blood:	n/a
44	chr13:66322551-66322601	Hela-S3	cervix:	n/a
45	chr13:66322551-66322601	GM19239	blood:	n/a
46	chr13:66322551-66322601	AG10803	skin:	n/a
47	chr13:66322551-66322601	HRE	kidney:	n/a
48	chr13:66322551-66322601	HEEpiC	esophagus:	n/a
49	chr13:66322551-66322601	HCM	heart:	n/a
50	chr13:66322551-66322601	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
2	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
3	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
4	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
5	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
6	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:

Variant related genes	Relation type
HNRNPA3P5	TF binding region
HNRNPA3P5	CpG island
ENSG00000236565	chromatin interactions

Extended variants
information (count: 1032 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549161686	chr13:66298132-66298133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566213617	chr13:66298146-66298147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189171760	chr13:66298152-66298153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375424063	chr13:66298160-66298161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541490992	chr13:66298177-66298178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4098535	chr13:66298181-66298182	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571951006	chr13:66298183-66298184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537709480	chr13:66298185-66298186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373182647	chr13:66298273-66298274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182150090	chr13:66298289-66298290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574109889	chr13:66298320-66298321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536855295	chr13:66298350-66298351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116457653	chr13:66298360-66298361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571848688	chr13:66298364-66298365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578094972	chr13:66298371-66298372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540608023	chr13:66298383-66298384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563766827	chr13:66298436-66298437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186865844	chr13:66298458-66298459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543273157	chr13:66298467-66298468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563604276	chr13:66298504-66298505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7992551	chr13:66298543-66298544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549202868	chr13:66298626-66298627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74789345	chr13:66298628-66298629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528627963	chr13:66298638-66298639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372506088	chr13:66298657-66298658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563689043	chr13:66298667-66298668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551929471	chr13:66298669-66298670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9571466	chr13:66298690-66298691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537448036	chr13:66298698-66298699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550944712	chr13:66298709-66298710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567993439	chr13:66298722-66298723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536434044	chr13:66298738-66298739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543050186	chr13:66298758-66298759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144408296	chr13:66298760-66298761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377651745	chr13:66298764-66298765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190057995	chr13:66298778-66298779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534385800	chr13:66298797-66298798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557441169	chr13:66298798-66298799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182126907	chr13:66298801-66298802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529918573	chr13:66298805-66298806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143139948	chr13:66298813-66298814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185608840	chr13:66298816-66298817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190425801	chr13:66298819-66298820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542439573	chr13:66298839-66298840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146403343	chr13:66298860-66298861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377643820	chr13:66298868-66298869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370148343	chr13:66298920-66298921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528308870	chr13:66298939-66298940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370859763	chr13:66298985-66298986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551855517	chr13:66298986-66298987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	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
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	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
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66298000-66298800	Enhancers	Dnd41	blood
2	chr13:66298200-66298600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:66298200-66298600	Enhancers	Fetal Stomach	stomach
4	chr13:66298200-66298800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr13:66298200-66298800	Enhancers	Fetal Kidney	kidney
6	chr13:66298200-66298800	Enhancers	NHDF-Ad	bronchial
7	chr13:66298200-66299400	Enhancers	Fetal Lung	lung
8	chr13:66298200-66299800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:66298200-66300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:66298800-66299200	Weak transcription	Fetal Kidney	kidney
11	chr13:66299200-66299800	Enhancers	Fetal Kidney	kidney
12	chr13:66299400-66299800	Enhancers	Fetal Heart	heart
13	chr13:66307000-66307600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:66318200-66319600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:66318400-66318800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr13:66318400-66319600	Enhancers	Osteobl	bone
17	chr13:66318800-66319000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr13:66318800-66319400	Enhancers	Adipose Nuclei	Adipose
19	chr13:66318800-66320600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr13:66319000-66319600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:66330600-66331400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
22	chr13:66336600-66337200	Enhancers	Fetal Kidney	kidney
23	chr13:66342600-66343200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr13:66343000-66343400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr13:66343000-66343400	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr13:66347000-66347200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:66347200-66349800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:66357600-66358000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr13:66358000-66358400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr13:66363800-66364200	Enhancers	Osteobl	bone
31	chr13:66363800-66364600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:66363800-66364600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:66363800-66364600	Enhancers	HSMMtube	muscle
34	chr13:66364200-66364600	Flanking Active TSS	Osteobl	bone
35	chr13:66372000-66373600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:66373600-66376400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:66376400-66377200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:66376600-66377000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:66377000-66379000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr13:66377200-66379000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:66379000-66379200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:66379000-66379400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:66379200-66379600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:66379400-66382200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:66379600-66379800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr13:66379800-66382400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:66380800-66382000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr13:66381000-66382800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr13:66381000-66382800	Enhancers	Osteobl	bone
50	chr13:66381400-66383200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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