Variant report

Variant	nsv832639
Chromosome Location	chr13:67049800-67223701
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	ARID3A	chr13:67192956-67193156	K562	blood:	n/a	n/a
2	ARID3A	chr13:67142089-67142310	K562	blood:	n/a	n/a
3	BACH1	chr13:67132673-67133003	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:67078100-67078397	H1-hESC	embryonic stem cell:	n/a	chr13:67078231-67078245
5	BATF	chr13:67052441-67052616	GM12878	blood:	n/a	n/a
6	BATF	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:67159926-67160259	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:67214443-67214833	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:67218623-67218628	GM12878	blood:	n/a	n/a
10	BRCA1	chr13:67088395-67088424	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr13:67137257-67137558	K562	blood:	n/a	n/a
12	CCNT2	chr13:67142117-67142330	K562	blood:	n/a	n/a
13	CEBPB	chr13:67160712-67161041	HepG2	liver:	n/a	chr13:67160889-67160900 chr13:67160891-67160902 chr13:67160822-67160833 chr13:67160891-67160900
14	CEBPB	chr13:67077994-67078240	A549	lung:	n/a	n/a
15	CEBPB	chr13:67103680-67103817	K562	blood:	n/a	chr13:67103735-67103748 chr13:67103735-67103748 chr13:67103735-67103746 chr13:67103796-67103807
16	CEBPB	chr13:67122102-67122405	HepG2	liver:	n/a	chr13:67122290-67122303 chr13:67122290-67122303 chr13:67122290-67122301 chr13:67122228-67122237 chr13:67122227-67122238 chr13:67122290-67122303 chr13:67122290-67122301
17	CEBPB	chr13:67160722-67161032	A549	lung:	n/a	chr13:67160889-67160900 chr13:67160891-67160902 chr13:67160822-67160833 chr13:67160891-67160900
18	CEBPB	chr13:67082284-67083068	Hela-S3	cervix:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707
19	CEBPB	chr13:67134434-67134888	K562	blood:	n/a	chr13:67134725-67134736
20	CEBPB	chr13:67208642-67208947	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:67130505-67130814	IMR90	lung:	n/a	n/a
22	CEBPB	chr13:67209643-67210073	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:67182388-67182540	K562	blood:	n/a	chr13:67182412-67182423 chr13:67182414-67182423
24	CEBPB	chr13:67081072-67081476	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:67130497-67130793	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:67082285-67083002	IMR90	lung:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707
27	CEBPB	chr13:67075269-67075708	A549	lung:	n/a	n/a
28	CEBPB	chr13:67082342-67082558	K562	blood:	n/a	chr13:67082473-67082484
29	CEBPB	chr13:67134638-67134723	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:67082302-67082679	H1-hESC	embryonic stem cell:	n/a	chr13:67082473-67082484
31	CEBPB	chr13:67130559-67130736	A549	lung:	n/a	n/a
32	CEBPB	chr13:67106195-67106574	IMR90	lung:	n/a	n/a
33	CEBPB	chr13:67134562-67134910	HepG2	liver:	n/a	chr13:67134725-67134736
34	CEBPB	chr13:67082292-67082664	HepG2	liver:	n/a	chr13:67082473-67082484
35	CEBPB	chr13:67082246-67082701	MCF-7	breast:	n/a	chr13:67082473-67082484
36	CEBPB	chr13:67082306-67082697	ECC-1	luminal epithelium:	n/a	chr13:67082473-67082484
37	CEBPB	chr13:67116340-67116460	A549	lung:	n/a	n/a
38	CEBPB	chr13:67082285-67082684	K562	blood:	n/a	chr13:67082473-67082484
39	CEBPB	chr13:67160725-67161052	IMR90	lung:	n/a	chr13:67160889-67160900 chr13:67160891-67160902 chr13:67160822-67160833 chr13:67160891-67160900
40	CEBPB	chr13:67077959-67078370	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr13:67082251-67082727	A549	lung:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707
42	CEBPB	chr13:67209677-67210025	IMR90	lung:	n/a	n/a
43	CEBPB	chr13:67066668-67066956	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:67082274-67082614	ECC-1	luminal epithelium:	n/a	chr13:67082473-67082484
45	CEBPB	chr13:67082287-67082669	MCF-7	breast:	n/a	chr13:67082473-67082484
46	CEBPB	chr13:67075285-67075687	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:67082287-67082928	A549	lung:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707
48	CEBPB	chr13:67082184-67082860	A549	lung:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707
49	CEBPB	chr13:67075293-67075671	IMR90	lung:	n/a	n/a
50	CEBPD	chr13:67142069-67142448	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67197277-67197327	AG09309	skin:	n/a
2	chr13:67101887-67101937	BE2_C	brain:	n/a
3	chr13:67155091-67155141	Caco-2	colon:	n/a
4	chr13:67155091-67155141	HNPCEpiC	eye:	n/a
5	chr13:67197133-67197183	NHBE	bronchial:	n/a
6	chr13:67197133-67197183	GM12892	blood:	n/a
7	chr13:67101887-67101937	Hela-S3	cervix:	n/a
8	chr13:67101887-67101937	ProgFib	skin:	n/a
9	chr13:67155091-67155141	SK-N-SH_RA	brain:	n/a
10	chr13:67101887-67101937	GM19239	blood:	n/a
11	chr13:67196386-67196436	MCF-7	breast:	n/a
12	chr13:67196386-67196436	PANC-1	pancreas:	n/a
13	chr13:67197277-67197327	AG04450	lung:	fetal
14	chr13:67197173-67197223	AG09319	gingival:	n/a
15	chr13:67197133-67197183	SK-N-SH_RA	brain:	n/a
16	chr13:67196386-67196436	ECC-1	luminal epithelium:	n/a
17	chr13:67196386-67196436	HCM	heart:	n/a
18	chr13:67197173-67197223	HEK293	kidney:	embryo
19	chr13:67197277-67197327	NH-A	brain:	n/a
20	chr13:67197277-67197327	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:67155091-67155141	HCPEpiC	choroid plexus:	n/a
22	chr13:67101887-67101937	HCF	heart:	n/a
23	chr13:67197277-67197327	SK-N-MC	brain:	n/a
24	chr13:67197173-67197223	RPTEC	kidney:	n/a
25	chr13:67197173-67197223	GM12878	blood:	n/a
26	chr13:67155091-67155141	GM12878	blood:	n/a
27	chr13:67197173-67197223	K562	blood:	n/a
28	chr13:67196386-67196436	NH-A	brain:	n/a
29	chr13:67155091-67155141	A549	lung:	n/a
30	chr13:67155091-67155141	NB4	blood:	n/a
31	chr13:67197173-67197223	AG10803	skin:	n/a
32	chr13:67196386-67196436	LNCaP	prostate:	n/a
33	chr13:67197173-67197223	SKMC	muscle:	n/a
34	chr13:67197173-67197223	Hepatocyte	liver:	n/a
35	chr13:67155091-67155141	SKMC	muscle:	n/a
36	chr13:67101887-67101937	HRE	kidney:	n/a
37	chr13:67197133-67197183	LNCaP	prostate:	n/a
38	chr13:67197133-67197183	Hepatocyte	liver:	n/a
39	chr13:67155091-67155141	RPTEC	kidney:	n/a
40	chr13:67197133-67197183	NH-A	brain:	n/a
41	chr13:67196386-67196436	PrEC	prostate:	n/a
42	chr13:67197277-67197327	PrEC	prostate:	n/a
43	chr13:67197173-67197223	SAEC	small airway:	n/a
44	chr13:67197173-67197223	PANC-1	pancreas:	n/a
45	chr13:67196386-67196436	SK-N-SH	brain:	n/a
46	chr13:67197277-67197327	NHDF-neo	bronchial:	n/a
47	chr13:67197133-67197183	PrEC	prostate:	n/a
48	chr13:67155091-67155141	MCF10A-Er-Src	breast:	n/a
49	chr13:67196386-67196436	Hepatocyte	liver:	n/a
50	chr13:67155091-67155141	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
2	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
3	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
4	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
5	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
6	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
7	chr13:67204110..67206444-chr13:67209007..67211337,2	K562	blood:
8	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
9	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
10	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
11	chr13:67066396..67067204-chr13:67263202..67263856,3	MCF-7	breast:
12	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
13	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
14	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
15	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
16	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
17	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
18	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
19	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
20	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
21	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:

Variant related genes	Relation type
RNU7-87P	TF binding region
RNU7-87P	CpG island
ENSG00000238500	chromatin interactions

Extended variants
information (count: 4635 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4635 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141429240	chr13:67049806-67049807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534043931	chr13:67049816-67049817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376178245	chr13:67049840-67049841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570785869	chr13:67049884-67049885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539435069	chr13:67049885-67049886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556236946	chr13:67049896-67049897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144569811	chr13:67049929-67049930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61957636	chr13:67049971-67049972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541336231	chr13:67049977-67049978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555654254	chr13:67049986-67049987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138523890	chr13:67050043-67050044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551643901	chr13:67050094-67050095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs920863	chr13:67050121-67050122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs555720905	chr13:67050132-67050133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577957917	chr13:67050160-67050161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543371003	chr13:67050161-67050162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563702162	chr13:67050164-67050165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12876635	chr13:67050187-67050188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543282297	chr13:67051604-67051605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563596318	chr13:67051639-67051640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147442586	chr13:67051656-67051657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562993730	chr13:67051676-67051677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183221674	chr13:67051749-67051750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528139128	chr13:67051756-67051757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140713180	chr13:67051823-67051824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149779602	chr13:67051888-67051889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113028032	chr13:67051934-67051935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542634965	chr13:67051953-67051954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187913652	chr13:67051975-67051976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567905904	chr13:67051992-67051993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536550452	chr13:67052035-67052036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145753613	chr13:67052063-67052064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573291858	chr13:67052066-67052067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545456014	chr13:67052076-67052077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376509718	chr13:67052216-67052217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559073460	chr13:67052270-67052271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191772764	chr13:67052272-67052273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183554753	chr13:67052343-67052344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563340648	chr13:67052375-67052376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529158364	chr13:67052376-67052377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76609306	chr13:67052377-67052378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188734080	chr13:67052380-67052381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528053895	chr13:67052396-67052397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551006827	chr13:67052400-67052401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570998287	chr13:67052413-67052414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530527402	chr13:67052421-67052422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192571772	chr13:67052459-67052460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11839087	chr13:67052472-67052473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9571587	chr13:67052476-67052477	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536919298	chr13:67052496-67052497	Enhancers	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
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
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67048200-67050200	Enhancers	Fetal Brain Male	brain
2	chr13:67049800-67050000	Enhancers	Aorta	Aorta
3	chr13:67051600-67052800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:67055200-67055600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr13:67056200-67056400	Enhancers	Brain Cingulate Gyrus	brain
6	chr13:67056400-67066800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr13:67056600-67056800	Enhancers	Brain Angular Gyrus	brain
8	chr13:67057000-67057800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr13:67057400-67057600	Enhancers	Brain Angular Gyrus	brain
10	chr13:67063400-67063800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:67064800-67066200	Enhancers	Fetal Lung	lung
12	chr13:67066800-67067000	Enhancers	Brain Cingulate Gyrus	brain
13	chr13:67066800-67067200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:67066800-67067200	Enhancers	A549	lung
15	chr13:67067000-67069600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr13:67067200-67075200	Weak transcription	A549	lung
17	chr13:67069200-67075200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr13:67069800-67070000	Enhancers	Brain Cingulate Gyrus	brain
19	chr13:67073800-67074200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:67074200-67075200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr13:67075200-67075800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr13:67075200-67076000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr13:67075200-67078800	Enhancers	A549	lung
24	chr13:67075400-67075600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr13:67075600-67075800	Enhancers	HSMM	muscle
26	chr13:67075600-67076000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr13:67075600-67076200	Enhancers	HSMMtube	muscle
28	chr13:67075800-67076800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr13:67075800-67078000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr13:67076000-67077800	Weak transcription	HSMM	muscle
31	chr13:67076000-67081000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:67076000-67087600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr13:67076200-67078000	Weak transcription	HSMMtube	muscle
34	chr13:67076800-67078800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr13:67077000-67078800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr13:67077000-67079200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr13:67077200-67077400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:67077200-67078600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:67077200-67078800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr13:67077200-67079000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr13:67077200-67079200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr13:67077400-67078000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:67077800-67078200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr13:67077800-67078400	Enhancers	HSMM	muscle
45	chr13:67078000-67078200	Enhancers	HSMMtube	muscle
46	chr13:67078000-67078400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr13:67078000-67078800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr13:67078000-67078800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr13:67078000-67079000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr13:67078000-67079000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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