Variant report

Variant	nsv886211
Chromosome Location	chr6:77208816-77317683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:77272270-77272992	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:77271069-77271494	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:77283185-77283204	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:77228168-77228521	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:77219241-77219437	GM12878	blood:	n/a	chr6:77219332-77219343
6	BRCA1	chr6:77271283-77271621	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:77292633-77292981	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:77292641-77292990	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:77292690-77292979	MCF-7	breast:	n/a	n/a
10	CEBPB	chr6:77222364-77222689	HepG2	liver:	n/a	chr6:77222528-77222539
11	CEBPB	chr6:77292690-77292951	A549	lung:	n/a	n/a
12	CEBPB	chr6:77292654-77292991	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:77270671-77271457	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:77225453-77225545	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:77258211-77258468	HepG2	liver:	n/a	chr6:77258347-77258360 chr6:77258347-77258358 chr6:77258349-77258360
16	CEBPB	chr6:77303904-77304153	HepG2	liver:	n/a	chr6:77304017-77304028
17	CEBPB	chr6:77273322-77273624	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:77273332-77273682	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:77273334-77273659	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:77222375-77222632	IMR90	lung:	n/a	chr6:77222528-77222539
21	CHD1	chr6:77271046-77273553	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr6:77294414-77294455	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr6:77274462-77275324	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr6:77306735-77306899	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr6:77271136-77271457	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr6:77303098-77303102	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr6:77238680-77238719	LNCaP	prostate:	n/a	n/a
28	CTCF	chr6:77211510-77211575	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:77211495-77211569	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:77235950-77235982	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:77211660-77211810	HCT-116	colon:	n/a	n/a
32	CTCF	chr6:77211492-77211561	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:77243008-77243025	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:77211380-77211530	HCT-116	colon:	n/a	n/a
35	CTCF	chr6:77315960-77316110	AG09319	gingival:	n/a	n/a
36	CTCF	chr6:77233308-77233386	ProgFib	skin:	n/a	n/a
37	CTCF	chr6:77314846-77314886	GM10266	blood:	n/a	n/a
38	CTCF	chr6:77235924-77235938	Fibrobl	skin:	n/a	n/a
39	E2F4	chr6:77244979-77245186	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr6:77283024-77283454	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F6	chr6:77303731-77304201	H1-hESC	embryonic stem cell:	n/a	n/a
42	E2F6	chr6:77270499-77270810	H1-hESC	embryonic stem cell:	n/a	n/a
43	E2F6	chr6:77264756-77265293	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr6:77264891-77265202	H1-hESC	embryonic stem cell:	n/a	chr6:77265079-77265089
45	FAM48A	chr6:77297527-77297652	GM12878	blood:	n/a	n/a
46	FOS	chr6:77228173-77228517	MCF10A-Er-Src	breast:	n/a	chr6:77228364-77228375
47	FOS	chr6:77228173-77228535	HUVEC	blood vessel:	n/a	chr6:77228364-77228375
48	FOS	chr6:77228207-77228537	MCF10A-Er-Src	breast:	n/a	chr6:77228364-77228375
49	FOS	chr6:77228176-77228525	MCF10A-Er-Src	breast:	n/a	chr6:77228364-77228375
50	FOS	chr6:77297221-77297659	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:77291523-77291573	BJ	skin:	n/a
2	chr6:77265160-77265210	ProgFib	skin:	n/a
3	chr6:77291523-77291573	K562	blood:	n/a
4	chr6:77291523-77291573	AG09319	gingival:	n/a
5	chr6:77265160-77265210	HIPEpiC	eye:	n/a
6	chr6:77265160-77265210	PFSK-1	brain:	n/a
7	chr6:77291523-77291573	SK-N-MC	brain:	n/a
8	chr6:77291523-77291573	HIPEpiC	eye:	n/a
9	chr6:77265160-77265210	H1-hESC	embryonic stem cell:	embryo
10	chr6:77291523-77291573	HL-60	blood:	n/a
11	chr6:77265160-77265210	HMEC	breast:	n/a
12	chr6:77291523-77291573	ProgFib	skin:	n/a
13	chr6:77291523-77291573	NB4	blood:	n/a
14	chr6:77291523-77291573	PrEC	prostate:	n/a
15	chr6:77265160-77265210	NB4	blood:	n/a
16	chr6:77265160-77265210	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:77291523-77291573	ECC-1	luminal epithelium:	n/a
18	chr6:77265160-77265210	BE2_C	brain:	n/a
19	chr6:77291523-77291573	Jurkat	blood:	n/a
20	chr6:77291523-77291573	HRCEpiC	kidney:	n/a
21	chr6:77291523-77291573	HepG2	liver:	n/a
22	chr6:77291523-77291573	GM12891	blood:	n/a
23	chr6:77265160-77265210	SKMC	muscle:	n/a
24	chr6:77265160-77265210	CMK	blood:	n/a
25	chr6:77291523-77291573	MCF10A-Er-Src	breast:	n/a
26	chr6:77265160-77265210	HepG2	liver:	n/a
27	chr6:77291523-77291573	HUVEC	blood vessel:	n/a
28	chr6:77291523-77291573	HCF	heart:	n/a
29	chr6:77291523-77291573	GM12878	blood:	n/a
30	chr6:77265160-77265210	AG10803	skin:	n/a
31	chr6:77265160-77265210	HCT-116	colon:	n/a
32	chr6:77265160-77265210	NHDF-neo	bronchial:	n/a
33	chr6:77265160-77265210	AG09309	skin:	n/a
34	chr6:77265160-77265210	SK-N-SH_RA	brain:	n/a
35	chr6:77291523-77291573	HRE	kidney:	n/a
36	chr6:77291523-77291573	HAEpiC	amniotic membrane:	n/a
37	chr6:77291523-77291573	HNPCEpiC	eye:	n/a
38	chr6:77291523-77291573	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:77291523-77291573	GM06990	blood:	n/a
40	chr6:77291523-77291573	NH-A	brain:	n/a
41	chr6:77291523-77291573	Hela-S3	cervix:	n/a
42	chr6:77265160-77265210	SK-N-MC	brain:	n/a
43	chr6:77265160-77265210	MCF-7	breast:	n/a
44	chr6:77265160-77265210	LNCaP	prostate:	n/a
45	chr6:77265160-77265210	HCPEpiC	choroid plexus:	n/a
46	chr6:77265160-77265210	AG04449	skin:	fetal
47	chr6:77265160-77265210	HNPCEpiC	eye:	n/a
48	chr6:77291523-77291573	HEEpiC	esophagus:	n/a
49	chr6:77265160-77265210	SK-N-SH	brain:	n/a
50	chr6:77291523-77291573	MCF-7	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:77258609..77260545-chr6:77270279..77272860,2	K562	blood:
2	chr1:11967926..11968691-chr6:77296332..77297332,3	Hela-S3	cervix:
3	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:
4	chr6:77258609..77260545-chr6:77270279..77272860,2	K562	blood:
5	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-2	chr6:77303246-77303340	ENSG00000236635
2	lnc-IMPG1-1	chr6:77303244-77303340	ENSG00000236635.2
3	lnc-MYO6-2	chr6:77232168-77232521	ENSG00000236635
4	lnc-MYO6-8	chr6:77288887-77289240	NONHSAT113643
5	lnc-IMPG1-1	chr6:77296165-77296283	ENSG00000236635.2
6	lnc-MYO6-2	chr6:77296166-77296285	ENSG00000236635
7	lnc-IMPG1-1	chr6:77232168-77232521	ENSG00000236635.2
8	lnc-MYO6-2	chr6:77296178-77296285	XLOC_005354
9	lnc-MYO6-2	chr6:77303246-77303510	XLOC_005354

No data

Variant related genes	Relation type
ENSG00000236635	TF binding region
ENSG00000272445	TF binding region
ENSG00000236635	CpG island
ENSG00000272445	CpG island
ENSG00000199347	chromatin interactions
JAK1	miRNA target sites

Extended variants
information (count: 2868 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2868 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116409039	chr6:77216215-77216216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574597152	chr6:77216233-77216234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146393142	chr6:77216335-77216336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540189099	chr6:77216439-77216440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550631280	chr6:77216442-77216443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569119506	chr6:77216460-77216461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536295174	chr6:77216468-77216469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548209309	chr6:77216470-77216471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373715790	chr6:77216486-77216487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562849981	chr6:77216492-77216493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533886076	chr6:77216498-77216499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558590941	chr6:77216537-77216538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369109631	chr6:77216542-77216543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556284611	chr6:77216579-77216580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578129964	chr6:77216655-77216656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139700656	chr6:77216732-77216733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115794978	chr6:77216762-77216763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575890353	chr6:77216772-77216773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563160490	chr6:77216793-77216794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373912727	chr6:77216796-77216797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542868303	chr6:77216858-77216859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73462802	chr6:77216871-77216872	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572867399	chr6:77216912-77216913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144359680	chr6:77216928-77216929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565360666	chr6:77216951-77216952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532244631	chr6:77216971-77216972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558312387	chr6:77216979-77216980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146700388	chr6:77216989-77216990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562689170	chr6:77217002-77217003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530023121	chr6:77217060-77217061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112222252	chr6:77217136-77217137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566494310	chr6:77217158-77217159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149899721	chr6:77217159-77217160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552020047	chr6:77217174-77217175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191887014	chr6:77217190-77217191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538909037	chr6:77217193-77217194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112887453	chr6:77217245-77217246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73464703	chr6:77217266-77217267	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs368134226	chr6:77217273-77217274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577061497	chr6:77217278-77217279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35711342	chr6:77217285-77217286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575394522	chr6:77217292-77217293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182952159	chr6:77217318-77217319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552216378	chr6:77217343-77217344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111776075	chr6:77217365-77217366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544125718	chr6:77217376-77217377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370444196	chr6:77217390-77217391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187667821	chr6:77217406-77217407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572932558	chr6:77217438-77217439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75052637	chr6:77217481-77217482	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77216200-77216600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:77216200-77217800	Enhancers	Fetal Lung	lung
3	chr6:77217800-77222400	Weak transcription	Fetal Lung	lung
4	chr6:77219800-77221000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:77222400-77222800	Enhancers	Fetal Lung	lung
6	chr6:77225400-77226200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:77244800-77245200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:77244800-77245200	Enhancers	Dnd41	blood
9	chr6:77245200-77257800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:77247400-77247600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:77247800-77248000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:77257600-77258000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:77257600-77258400	Enhancers	Fetal Heart	heart
14	chr6:77257800-77258000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:77257800-77258000	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:77258000-77266000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr6:77258400-77258800	Weak transcription	Fetal Heart	heart
18	chr6:77258800-77259400	Enhancers	Fetal Heart	heart
19	chr6:77259400-77261000	Weak transcription	Fetal Heart	heart
20	chr6:77261000-77263200	Enhancers	Fetal Heart	heart
21	chr6:77263200-77268000	Weak transcription	Fetal Heart	heart
22	chr6:77264200-77265000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:77264200-77265000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr6:77264200-77265000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:77264400-77264600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:77264400-77265000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr6:77264400-77265000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:77264600-77264800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr6:77264600-77267400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:77264800-77265000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr6:77264800-77267600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr6:77265000-77266800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr6:77265000-77266800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr6:77265000-77267400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:77265000-77267400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:77265000-77267600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr6:77265200-77267600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr6:77266000-77266200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:77266200-77266600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr6:77266600-77270400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:77266800-77267000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:77266800-77270800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:77267000-77267400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr6:77267400-77267600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:77267400-77267600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr6:77267400-77268400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:77267400-77268600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:77267400-77270000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:77267600-77267800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr6:77267600-77268000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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