Variant report

Variant	esv2759465
Chromosome Location	chr6:117431224-117627275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:1708)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:117548019-117548316	HepG2	liver:	n/a	n/a
2	ATF2	chr6:117586060-117586371	GM12878	blood:	n/a	n/a
3	BACH1	chr6:117586712-117586778	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:117591194-117591325	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:117592194-117592308	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:117459342-117459361	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:117593759-117594104	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:117561663-117561856	GM12878	blood:	n/a	n/a
9	BCL3	chr6:117442363-117442670	GM12878	blood:	n/a	n/a
10	CBX3	chr6:117488717-117489231	HCT-116	colon:	n/a	n/a
11	CCNT2	chr6:117538241-117538436	K562	blood:	n/a	n/a
12	CCNT2	chr6:117476295-117476440	K562	blood:	n/a	n/a
13	CCNT2	chr6:117620327-117620446	K562	blood:	n/a	n/a
14	CEBPB	chr6:117587004-117587185	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:117516918-117517266	Hela-S3	cervix:	n/a	chr6:117517085-117517096
16	CEBPB	chr6:117432748-117432961	HepG2	liver:	n/a	chr6:117432811-117432822
17	CEBPB	chr6:117548007-117548706	HepG2	liver:	n/a	chr6:117548497-117548508 chr6:117548495-117548506
18	CEBPB	chr6:117486492-117486632	HepG2	liver:	n/a	chr6:117486549-117486560 chr6:117486549-117486562 chr6:117486551-117486562
19	CEBPB	chr6:117554591-117554700	A549	lung:	n/a	chr6:117554655-117554666
20	CEBPB	chr6:117554489-117554800	HepG2	liver:	n/a	chr6:117554655-117554666
21	CEBPB	chr6:117439668-117439869	HepG2	liver:	n/a	chr6:117439757-117439768 chr6:117439759-117439770 chr6:117439757-117439770 chr6:117439754-117439771 chr6:117439757-117439770
22	CEBPB	chr6:117549961-117550163	HepG2	liver:	n/a	chr6:117550075-117550086
23	CEBPB	chr6:117516940-117517351	HCT-116	colon:	n/a	chr6:117517085-117517096
24	CEBPB	chr6:117516938-117517254	H1-hESC	embryonic stem cell:	n/a	chr6:117517085-117517096
25	CEBPB	chr6:117560505-117560830	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:117550047-117550129	A549	lung:	n/a	chr6:117550075-117550086
27	CEBPB	chr6:117516923-117517217	HepG2	liver:	n/a	chr6:117517085-117517096
28	CEBPB	chr6:117591356-117591416	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:117442319-117442608	HepG2	liver:	n/a	chr6:117442451-117442462 chr6:117442489-117442500
30	CEBPB	chr6:117516814-117517281	HCT-116	colon:	n/a	chr6:117517085-117517096
31	CEBPB	chr6:117601351-117601551	HepG2	liver:	n/a	chr6:117601467-117601478
32	CHD1	chr6:117592127-117592222	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr6:117591181-117591739	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:117603480-117603676	K562	blood:	n/a	n/a
35	CHD2	chr6:117586262-117586360	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:117591297-117591320	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr6:117586600-117587155	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr6:117586727-117587425	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr6:117591168-117592322	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr6:117585407-117586358	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr6:117510100-117510250	Caco-2	colon:	n/a	chr6:117510166-117510184
42	CTCF	chr6:117510039-117510254	A549	lung:	n/a	chr6:117510166-117510184
43	CTCF	chr6:117488860-117489010	HMEC	breast:	n/a	n/a
44	CTCF	chr6:117510180-117510330	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr6:117510060-117510210	AoAF	blood vessel:	n/a	chr6:117510166-117510184
46	CTCF	chr6:117589284-117589721	K562	blood:	n/a	n/a
47	CTCF	chr6:117510100-117510250	AG09319	gingival:	n/a	chr6:117510166-117510184
48	CTCF	chr6:117573590-117573608	GM10248	blood:	n/a	n/a
49	CTCF	chr6:117510120-117510270	HRPEpiC	eye:	n/a	chr6:117510166-117510184
50	CTCF	chr6:117510160-117510310	GM12878	blood:	n/a	chr6:117510166-117510184

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:117503272-117503322	T-47D	breast:	n/a
2	chr6:117584815-117584865	SK-N-SH	brain:	n/a
3	chr6:117591534-117591584	ovcar-3	ovarian:	n/a
4	chr6:117586538-117586588	ECC-1	luminal epithelium:	n/a
5	chr6:117592358-117592408	NT2-D1	testis:	n/a
6	chr6:117586575-117586625	HRE	kidney:	n/a
7	chr6:117591433-117591483	HRPEpiC	eye:	n/a
8	chr6:117591433-117591483	SK-N-MC	brain:	n/a
9	chr6:117586225-117586275	ProgFib	skin:	n/a
10	chr6:117587155-117587205	HUVEC	blood vessel:	n/a
11	chr6:117587588-117587638	Caco-2	colon:	n/a
12	chr6:117586225-117586275	PFSK-1	brain:	n/a
13	chr6:117591534-117591584	H1-hESC	embryonic stem cell:	embryo
14	chr6:117584815-117584865	SAEC	small airway:	n/a
15	chr6:117586681-117586731	NT2-D1	testis:	n/a
16	chr6:117586681-117586731	NH-A	brain:	n/a
17	chr6:117587588-117587638	HEEpiC	esophagus:	n/a
18	chr6:117591534-117591584	GM12892	blood:	n/a
19	chr6:117586817-117586867	HRPEpiC	eye:	n/a
20	chr6:117586593-117586643	AG04450	lung:	fetal
21	chr6:117503272-117503322	HEEpiC	esophagus:	n/a
22	chr6:117591827-117591877	CMK	blood:	n/a
23	chr6:117589651-117589701	PFSK-1	brain:	n/a
24	chr6:117586681-117586731	Hepatocyte	liver:	n/a
25	chr6:117591684-117591734	AG09309	skin:	n/a
26	chr6:117586918-117586968	AoSMC	blood vessel:	n/a
27	chr6:117586666-117586716	Hela-S3	cervix:	n/a
28	chr6:117609650-117609700	NT2-D1	testis:	n/a
29	chr6:117591433-117591483	PFSK-1	brain:	n/a
30	chr6:117586538-117586588	CMK	blood:	n/a
31	chr6:117584596-117584646	U87	brain:	n/a
32	chr6:117586225-117586275	AG04450	lung:	fetal
33	chr6:117585479-117585529	NHBE	bronchial:	n/a
34	chr6:117587155-117587205	AG04450	lung:	fetal
35	chr6:117583181-117583231	NT2-D1	testis:	n/a
36	chr6:117591827-117591877	MCF-7	breast:	n/a
37	chr6:117592262-117592312	AG10803	skin:	n/a
38	chr6:117503272-117503322	Caco-2	colon:	n/a
39	chr6:117586681-117586731	LNCaP	prostate:	n/a
40	chr6:117587588-117587638	SK-N-MC	brain:	n/a
41	chr6:117586575-117586625	AG09319	gingival:	n/a
42	chr6:117585815-117585865	HCF	heart:	n/a
43	chr6:117584596-117584646	MCF-7	breast:	n/a
44	chr6:117586817-117586867	Jurkat	blood:	n/a
45	chr6:117591433-117591483	SKMC	muscle:	n/a
46	chr6:117584715-117584765	GM06990	blood:	n/a
47	chr6:117586593-117586643	NHDF-neo	bronchial:	n/a
48	chr6:117584815-117584865	ProgFib	skin:	n/a
49	chr6:117589651-117589701	A549	lung:	n/a
50	chr6:117585815-117585865	IMR90	lung:	fetal

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:117456061..117457595-chr6:117459840..117462446,2	K562	blood:
2	chr6:117447258..117449659-chr6:117456353..117459059,2	K562	blood:
3	chr6:117432728..117435225-chr6:117439078..117441229,2	MCF-7	breast:
4	chr6:117293198..117294084-chr6:117602223..117602832,3	MCF-7	breast:
5	chr6:117290291..117290928-chr6:117516415..117517089,2	MCF-7	breast:
6	chr6:117601835..117602502-chr6:117638433..117639008,2	MCF-7	breast:
7	chr6:117456061..117457595-chr6:117459840..117462446,2	K562	blood:
8	chr6:116710278..116712360-chr6:117478553..117480106,2	K562	blood:
9	chr6:117447258..117449659-chr6:117456353..117459059,2	K562	blood:
10	chr6:117292562..117293807-chr6:117509373..117510214,3	MCF-7	breast:
11	chr6:117623559..117626369-chr6:117645253..117647045,2	K562	blood:
12	chr6:117432728..117435225-chr6:117439078..117441229,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL2-1	chr6:117620527-117620801	NONHSAT114667
2	lnc-ROS1-2	chr6:117585738-117585864	NONHSAT114666
3	lnc-ROS1-2	chr6:117583516-117584346	NONHSAT114666
4	lnc-VGLL2-2	chr6:117622618-117622921	NONHSAT114668

No data

Variant related genes	Relation type
VGLL2	TF binding region
RN7SKP51	TF binding region
RN7SKP18	TF binding region
VGLL2	CpG island
RN7SKP51	CpG island
RN7SKP18	CpG island

Extended variants
information (count: 5515 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5515 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564898035	chr6:117431804-117431805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532320476	chr6:117431817-117431818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547332309	chr6:117431850-117431851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544410095	chr6:117431873-117431874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557094482	chr6:117431874-117431875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529649104	chr6:117431893-117431894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114714712	chr6:117431911-117431912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569751212	chr6:117431919-117431920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140324503	chr6:117431920-117431921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552231629	chr6:117431952-117431953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571774980	chr6:117431963-117431964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149662609	chr6:117431965-117431966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554548734	chr6:117431966-117431967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566338332	chr6:117431972-117431973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536653138	chr6:117432002-117432003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs940985	chr6:117432110-117432111	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs369863900	chr6:117432139-117432140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576497505	chr6:117432212-117432213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543588536	chr6:117432229-117432230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189533421	chr6:117432265-117432266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182352870	chr6:117432272-117432273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145642121	chr6:117432281-117432282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73766166	chr6:117432334-117432335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529907469	chr6:117432353-117432354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541822905	chr6:117432390-117432391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563169840	chr6:117432411-117432412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530502429	chr6:117432438-117432439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536758546	chr6:117432449-117432450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552034455	chr6:117432484-117432485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77755897	chr6:117432520-117432521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532765063	chr6:117432523-117432524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547968016	chr6:117432594-117432595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs118054285	chr6:117432605-117432606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536912332	chr6:117432612-117432613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555229883	chr6:117432614-117432615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528418251	chr6:117432623-117432624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148896015	chr6:117432630-117432631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537443057	chr6:117432638-117432639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186467579	chr6:117432679-117432680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191311147	chr6:117432683-117432684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576878307	chr6:117432694-117432695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540848624	chr6:117432745-117432746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78942626	chr6:117432749-117432750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373094228	chr6:117432752-117432753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375661971	chr6:117432755-117432756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370247865	chr6:117432763-117432764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183573663	chr6:117432785-117432786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142618844	chr6:117432823-117432824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561564257	chr6:117432845-117432846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563594253	chr6:117432849-117432850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117431800-117432000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:117431800-117432200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:117432000-117432200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr6:117432200-117438600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:117432400-117435400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:117435400-117435600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:117435600-117440200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:117438200-117440000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:117438600-117439400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:117438800-117439200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:117439000-117439400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:117439000-117439400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:117446800-117448800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr6:117447400-117447800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:117447400-117448000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:117450000-117450200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr6:117450800-117451000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr6:117457800-117458000	Weak transcription	Psoas Muscle	Psoas
19	chr6:117457800-117459200	Enhancers	Left Ventricle	heart
20	chr6:117457800-117461400	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr6:117458000-117458200	Enhancers	Colon Smooth Muscle	Colon
22	chr6:117458000-117458200	Enhancers	Fetal Muscle Leg	muscle
23	chr6:117458000-117458200	Enhancers	Psoas Muscle	Psoas
24	chr6:117458000-117459000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:117458200-117460200	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:117458200-117460200	Weak transcription	Psoas Muscle	Psoas
27	chr6:117458400-117459600	Weak transcription	Colon Smooth Muscle	Colon
28	chr6:117459000-117459200	Enhancers	Fetal Heart	heart
29	chr6:117459000-117459600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr6:117459000-117460400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:117459200-117460000	Weak transcription	Fetal Heart	heart
32	chr6:117459200-117463000	Weak transcription	Left Ventricle	heart
33	chr6:117459600-117460600	Enhancers	Stomach Smooth Muscle	stomach
34	chr6:117459600-117461200	Enhancers	Colon Smooth Muscle	Colon
35	chr6:117459600-117461400	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr6:117459800-117460000	Enhancers	Fetal Brain Male	brain
37	chr6:117459800-117460600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:117459800-117461000	Enhancers	HSMMtube	muscle
39	chr6:117460000-117461000	Enhancers	Rectal Smooth Muscle	rectum
40	chr6:117460000-117461400	Enhancers	Adipose Nuclei	Adipose
41	chr6:117460000-117461400	Enhancers	Fetal Heart	heart
42	chr6:117460200-117461000	Enhancers	Fetal Muscle Leg	muscle
43	chr6:117460200-117461000	Enhancers	Psoas Muscle	Psoas
44	chr6:117460200-117461200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr6:117460400-117461400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:117460600-117461000	Enhancers	Brain Hippocampus Middle	brain
47	chr6:117460800-117461200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:117461000-117462800	Weak transcription	Fetal Muscle Leg	muscle
49	chr6:117461000-117462800	Weak transcription	Psoas Muscle	Psoas
50	chr6:117461200-117467000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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