Variant report

Variant	esv1798215
Chromosome Location	chr6:64487748-64544220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:826)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64512548-64512818	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64509356-64509581	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:64502828-64502906	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:64516019-64516583	HepG2	liver:	n/a	n/a
5	ATF3	chr6:64516012-64516622	A549	lung:	n/a	n/a
6	BATF	chr6:64509823-64510050	GM12878	blood:	n/a	n/a
7	BCL3	chr6:64516097-64516650	A549	lung:	n/a	n/a
8	BCL3	chr6:64516032-64516762	A549	lung:	n/a	n/a
9	BRCA1	chr6:64515968-64516744	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr6:64516057-64516555	HCT-116	colon:	n/a	n/a
11	CEBPB	chr6:64510827-64511000	HepG2	liver:	n/a	chr6:64510915-64510926
12	CEBPB	chr6:64529734-64530107	HepG2	liver:	n/a	chr6:64529929-64529940
13	CEBPB	chr6:64516011-64516857	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:64516000-64516850	HCT-116	colon:	n/a	n/a
15	CEBPB	chr6:64516083-64516765	HCT-116	colon:	n/a	n/a
16	CEBPB	chr6:64516164-64516661	A549	lung:	n/a	n/a
17	CEBPB	chr6:64516190-64516609	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:64514181-64514648	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:64502986-64503469	A549	lung:	n/a	chr6:64503400-64503411
20	CEBPB	chr6:64529788-64530058	A549	lung:	n/a	chr6:64529929-64529940
21	CEBPB	chr6:64515999-64516759	A549	lung:	n/a	n/a
22	CEBPB	chr6:64516140-64516596	A549	lung:	n/a	n/a
23	CEBPB	chr6:64516151-64516626	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:64529773-64530065	Hela-S3	cervix:	n/a	chr6:64529929-64529940
25	CEBPB	chr6:64515869-64516618	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:64502725-64503490	HepG2	liver:	n/a	chr6:64503400-64503411
27	CEBPB	chr6:64516212-64516545	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr6:64516253-64516536	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:64516116-64516669	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:64504842-64504844	K562	blood:	n/a	n/a
31	CEBPB	chr6:64510927-64511061	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:64529735-64530074	IMR90	lung:	n/a	chr6:64529929-64529940
33	CEBPB	chr6:64512478-64512975	HepG2	liver:	n/a	chr6:64512893-64512904 chr6:64512891-64512904 chr6:64512539-64512548 chr6:64512695-64512708 chr6:64512537-64512550 chr6:64512539-64512550
34	CHD2	chr6:64516070-64516537	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:64512600-64512750	RPTEC	kidney:	n/a	n/a
36	CTCF	chr6:64512620-64512770	AG04449	skin:	n/a	n/a
37	CTCF	chr6:64512600-64512750	NHEK	skin:	n/a	n/a
38	CTCF	chr6:64512620-64512770	HPF	lung:	n/a	n/a
39	CTCF	chr6:64512680-64512830	HAc	cerebellar:	n/a	n/a
40	CTCF	chr6:64527143-64527252	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr6:64523520-64523670	Caco-2	colon:	n/a	chr6:64523614-64523624 chr6:64523609-64523627
42	CTCF	chr6:64512640-64512790	HCFaa	heart:	n/a	n/a
43	CTCF	chr6:64527100-64527250	HPF	lung:	n/a	n/a
44	CTCF	chr6:64527100-64527250	AG04449	skin:	n/a	n/a
45	CTCF	chr6:64527120-64527270	AG04450	lung:	n/a	n/a
46	CTCF	chr6:64527120-64527270	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:64512580-64512730	GM12878	blood:	n/a	n/a
48	CTCF	chr6:64527120-64527270	GM12872	blood:	n/a	n/a
49	CTCF	chr6:64523560-64523710	HMF	breast:	n/a	chr6:64523614-64523624 chr6:64523609-64523627
50	CTCF	chr6:64512373-64513150	A549	lung:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64515007-64515057	HNPCEpiC	eye:	n/a
2	chr6:64515007-64515057	HNPCEpiC	eye:	n/a
3	chr6:64527786-64527836	GM12878	blood:	n/a
4	chr6:64527786-64527836	HEK293	kidney:	embryo
5	chr6:64527786-64527836	RPTEC	kidney:	n/a
6	chr6:64515007-64515057	AG04449	skin:	fetal
7	chr6:64527786-64527836	PANC-1	pancreas:	n/a
8	chr6:64515007-64515057	GM19239	blood:	n/a
9	chr6:64527786-64527836	SKMC	muscle:	n/a
10	chr6:64527786-64527836	AG04449	skin:	fetal
11	chr6:64527786-64527836	ovcar-3	ovarian:	n/a
12	chr6:64515007-64515057	Hepatocyte	liver:	n/a
13	chr6:64515007-64515057	SKMC	muscle:	n/a
14	chr6:64515007-64515057	GM12891	blood:	n/a
15	chr6:64515007-64515057	AG09319	gingival:	n/a
16	chr6:64515007-64515057	SK-N-SH	brain:	n/a
17	chr6:64527786-64527836	K562	blood:	n/a
18	chr6:64527786-64527836	SK-N-MC	brain:	n/a
19	chr6:64527786-64527836	HCPEpiC	choroid plexus:	n/a
20	chr6:64527786-64527836	HCM	heart:	n/a
21	chr6:64515007-64515057	HEEpiC	esophagus:	n/a
22	chr6:64515007-64515057	HCF	heart:	n/a
23	chr6:64527786-64527836	GM19239	blood:	n/a
24	chr6:64527786-64527836	CMK	blood:	n/a
25	chr6:64527786-64527836	MCF-7	breast:	n/a
26	chr6:64527786-64527836	SK-N-SH	brain:	n/a
27	chr6:64527786-64527836	Hela-S3	cervix:	n/a
28	chr6:64527786-64527836	AG10803	skin:	n/a
29	chr6:64527786-64527836	MCF10A-Er-Src	breast:	n/a
30	chr6:64515007-64515057	NHDF-neo	bronchial:	n/a
31	chr6:64527786-64527836	ECC-1	luminal epithelium:	n/a
32	chr6:64527786-64527836	SAEC	small airway:	n/a
33	chr6:64515007-64515057	HCT-116	colon:	n/a
34	chr6:64515007-64515057	CMK	blood:	n/a
35	chr6:64515007-64515057	SK-N-SH_RA	brain:	n/a
36	chr6:64515007-64515057	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:64527786-64527836	NB4	blood:	n/a
38	chr6:64515007-64515057	K562	blood:	n/a
39	chr6:64515007-64515057	BJ	skin:	n/a
40	chr6:64515007-64515057	HRPEpiC	eye:	n/a
41	chr6:64527786-64527836	PFSK-1	brain:	n/a
42	chr6:64515007-64515057	GM12892	blood:	n/a
43	chr6:64527786-64527836	NH-A	brain:	n/a
44	chr6:64515007-64515057	NT2-D1	testis:	n/a
45	chr6:64515007-64515057	ECC-1	luminal epithelium:	n/a
46	chr6:64515007-64515057	NH-A	brain:	n/a
47	chr6:64515007-64515057	PFSK-1	brain:	n/a
48	chr6:64515007-64515057	MCF10A-Er-Src	breast:	n/a
49	chr6:64527786-64527836	IMR90	lung:	fetal
50	chr6:64515007-64515057	A549	lung:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:64061604..64062576-chr6:64512267..64512790,2	MCF-7	breast:
2	chr6:64281819..64283796-chr6:64507632..64510704,3	MCF-7	breast:
3	chr6:64308255..64308783-chr6:64512237..64512792,2	MCF-7	breast:
4	chr6:64499118..64500868-chr6:64506115..64508701,2	K562	blood:
5	chr6:64062812..64063338-chr6:64512230..64512915,2	MCF-7	breast:
6	chr6:64503767..64506389-chr6:64511361..64513457,2	K562	blood:
7	chr6:64281948..64284181-chr6:64510881..64512793,2	MCF-7	breast:
8	chr6:64523219..64524103-chr6:65442776..65443345,2	MCF-7	breast:
9	chr6:64062103..64065068-chr6:64510364..64512443,2	MCF-7	breast:
10	chr6:64503767..64506389-chr6:64511361..64513457,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF3-1	chr6:64527231-64527298	NONHSAT113357
2	lnc-PHF3-1	chr6:64516729-64516779	ENSG00000236345.1
3	lnc-PHF3-1	chr6:64531133-64532559	NONHSAT113357
4	lnc-PHF3-6	chr6:64507082-64507924	NONHSAT113355
5	lnc-PHF3-5	chr6:64489031-64489229	NONHSAT113354
6	lnc-PHF3-1	chr6:64531133-64532535	ENSG00000236345.1
7	lnc-PHF3-5	chr6:64487498-64488136	NONHSAT113354

No data

Variant related genes	Relation type
ENSG00000236345	TF binding region
EYS	TF binding region
ENSG00000218813	TF binding region
ENSG00000236345	CpG island
EYS	CpG island
ENSG00000218813	CpG island
ENSG00000112245	chromatin interactions
ENSG00000218813	chromatin interactions
ENSG00000266680	chromatin interactions

Extended variants
information (count: 1491 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1491 , 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	rs115292685	chr6:64487754-64487755	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs553956077	chr6:64487854-64487855	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs557020239	chr6:64487887-64487888	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs559824825	chr6:64487929-64487930	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs374494800	chr6:64487955-64487956	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs368798160	chr6:64487986-64487987	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs74636274	chr6:64488001-64488002	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs557892188	chr6:64488046-64488047	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564020009	chr6:64488049-64488050	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs191846522	chr6:64488060-64488061	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs144282503	chr6:64488085-64488086	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs146094035	chr6:64488097-64488098	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs115940573	chr6:64488098-64488099	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs548427462	chr6:64488110-64488111	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs543672734	chr6:64488187-64488188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539123403	chr6:64488221-64488222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556158834	chr6:64488222-64488223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200712814	chr6:64488231-64488232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530805298	chr6:64488240-64488241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138209379	chr6:64488256-64488257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370588829	chr6:64488263-64488264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184039696	chr6:64488272-64488273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144942923	chr6:64488289-64488290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189499625	chr6:64488291-64488292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75428001	chr6:64488334-64488335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546495563	chr6:64488398-64488399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568235213	chr6:64488466-64488467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367977782	chr6:64488491-64488492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557281515	chr6:64488636-64488637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575355304	chr6:64488649-64488650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192158011	chr6:64488755-64488756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574328817	chr6:64488842-64488843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139666987	chr6:64488856-64488857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559101288	chr6:64488869-64488870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572419295	chr6:64488875-64488876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557866505	chr6:64488924-64488925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370880021	chr6:64488964-64488965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528838897	chr6:64488965-64488966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572866164	chr6:64489030-64489031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576396043	chr6:64489083-64489084	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs540293728	chr6:64489184-64489185	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs113078824	chr6:64489204-64489205	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs559979017	chr6:64489216-64489217	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs542157217	chr6:64489239-64489240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541433696	chr6:64489282-64489283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185883920	chr6:64489301-64489302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561163063	chr6:64489322-64489323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145597984	chr6:64489330-64489331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562405836	chr6:64489346-64489347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35119731	chr6:64489347-64489348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64485200-64514400	Weak transcription	Adipose Nuclei	Adipose
2	chr6:64487600-64487800	Enhancers	NHDF-Ad	bronchial
3	chr6:64492800-64493000	Enhancers	Liver	Liver
4	chr6:64492800-64493200	Active TSS	Duodenum Smooth Muscle	Duodenum
5	chr6:64493000-64493600	Flanking Active TSS	Liver	Liver
6	chr6:64493000-64493600	Enhancers	Duodenum Mucosa	Duodenum
7	chr6:64493000-64495800	Enhancers	GM12878-XiMat	blood
8	chr6:64493400-64495400	Enhancers	Stomach Mucosa	stomach
9	chr6:64493600-64494000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
10	chr6:64493600-64494200	ZNF genes & repeats	Liver	Liver
11	chr6:64494800-64495600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:64495000-64495400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:64495400-64498000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr6:64495600-64498000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:64495800-64499800	Weak transcription	GM12878-XiMat	blood
16	chr6:64496600-64497000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:64496600-64497800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr6:64497000-64497400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:64497000-64497400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr6:64497000-64514400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:64497400-64502800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr6:64497800-64503000	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr6:64498000-64499000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:64498000-64499200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:64498000-64499200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:64498200-64498800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:64498200-64499000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr6:64498200-64499000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:64498200-64499000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr6:64498200-64499200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:64498400-64499200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:64498600-64498800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:64498600-64499000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr6:64498800-64499200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr6:64498800-64499200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:64498800-64499200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr6:64498800-64499400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:64499000-64499200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
39	chr6:64499000-64499200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:64499000-64500400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr6:64499000-64503200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr6:64499000-64503200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:64499000-64503800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:64499800-64501800	Enhancers	GM12878-XiMat	blood
45	chr6:64500400-64500600	Enhancers	H9 Cell Line	embryonic stem cell
46	chr6:64500600-64500800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr6:64501800-64502600	Enhancers	Fetal Intestine Small	intestine
48	chr6:64501800-64503600	Weak transcription	GM12878-XiMat	blood
49	chr6:64501800-64504200	Enhancers	Fetal Intestine Large	intestine
50	chr6:64502000-64506200	Enhancers	Primary monocytes fromperipheralblood	blood

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