Variant report

Variant	nsv886207
Chromosome Location	chr6:77130167-77266188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:77151494-77151955	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:77151557-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:77151504-77151916	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:77151627-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:77148487-77148871	H1-hESC	embryonic stem cell:	n/a	chr6:77148663-77148677
6	BACH1	chr6:77228168-77228521	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:77176056-77176337	GM12878	blood:	n/a	chr6:77176197-77176208
8	BATF	chr6:77219241-77219437	GM12878	blood:	n/a	chr6:77219332-77219343
9	BATF	chr6:77176105-77176301	GM12878	blood:	n/a	chr6:77176197-77176208
10	BHLHE40	chr6:77176053-77176331	GM12878	blood:	n/a	n/a
11	CBX3	chr6:77205617-77206052	HCT-116	colon:	n/a	n/a
12	CEBPB	chr6:77151495-77151928	HepG2	liver:	n/a	chr6:77151746-77151757
13	CEBPB	chr6:77140266-77140742	IMR90	lung:	n/a	chr6:77140653-77140666 chr6:77140654-77140665 chr6:77140653-77140664
14	CEBPB	chr6:77133008-77133190	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:77140360-77140810	HepG2	liver:	n/a	chr6:77140653-77140666 chr6:77140654-77140665 chr6:77140653-77140664
16	CEBPB	chr6:77222375-77222632	IMR90	lung:	n/a	chr6:77222528-77222539
17	CEBPB	chr6:77258211-77258468	HepG2	liver:	n/a	chr6:77258347-77258360 chr6:77258347-77258358 chr6:77258349-77258360
18	CEBPB	chr6:77151408-77151975	H1-hESC	embryonic stem cell:	n/a	chr6:77151746-77151757
19	CEBPB	chr6:77225453-77225545	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:77151585-77151889	IMR90	lung:	n/a	chr6:77151746-77151757
21	CEBPB	chr6:77222364-77222689	HepG2	liver:	n/a	chr6:77222528-77222539
22	CHD1	chr6:77151523-77151703	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr6:77151555-77152013	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:77206264-77206321	LNCaP	prostate:	n/a	n/a
25	CTCF	chr6:77211510-77211575	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:77185100-77185250	GM12872	blood:	n/a	n/a
27	CTCF	chr6:77185174-77185229	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:77211380-77211530	HCT-116	colon:	n/a	n/a
29	CTCF	chr6:77202944-77202961	GM13976	blood:	n/a	n/a
30	CTCF	chr6:77202655-77202678	GM13976	blood:	n/a	n/a
31	CTCF	chr6:77204543-77204582	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:77243008-77243025	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:77235924-77235938	Fibrobl	skin:	n/a	n/a
34	CTCF	chr6:77161746-77161827	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:77238680-77238719	LNCaP	prostate:	n/a	n/a
36	CTCF	chr6:77158655-77158691	GM10248	blood:	n/a	n/a
37	CTCF	chr6:77161980-77161989	Fibrobl	skin:	n/a	n/a
38	CTCF	chr6:77233308-77233386	ProgFib	skin:	n/a	n/a
39	CTCF	chr6:77172584-77172678	Medullo	brain:	n/a	n/a
40	CTCF	chr6:77148127-77148152	ProgFib	skin:	n/a	n/a
41	CTCF	chr6:77148092-77148137	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:77211495-77211569	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:77211660-77211810	HCT-116	colon:	n/a	n/a
44	CTCF	chr6:77205051-77205114	GM13976	blood:	n/a	n/a
45	CTCF	chr6:77185120-77185270	HCT-116	colon:	n/a	n/a
46	CTCF	chr6:77204320-77204470	SAEC	small airway:	n/a	n/a
47	CTCF	chr6:77196805-77196874	GM10248	blood:	n/a	n/a
48	CTCF	chr6:77211492-77211561	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:77185100-77185250	HCT-116	colon:	n/a	n/a
50	CTCF	chr6:77185120-77185270	HEK293	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:77265160-77265210	A549	lung:	n/a
2	chr6:77265160-77265210	NH-A	brain:	n/a
3	chr6:77265160-77265210	ovcar-3	ovarian:	n/a
4	chr6:77265160-77265210	HCT-116	colon:	n/a
5	chr6:77265160-77265210	NHBE	bronchial:	n/a
6	chr6:77265160-77265210	AG09319	gingival:	n/a
7	chr6:77265160-77265210	T-47D	breast:	n/a
8	chr6:77265160-77265210	HEK293	kidney:	embryo
9	chr6:77265160-77265210	PFSK-1	brain:	n/a
10	chr6:77265160-77265210	MCF-7	breast:	n/a
11	chr6:77265160-77265210	BJ	skin:	n/a
12	chr6:77265160-77265210	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:77265160-77265210	Caco-2	colon:	n/a
14	chr6:77265160-77265210	H1-hESC	embryonic stem cell:	embryo
15	chr6:77265160-77265210	NB4	blood:	n/a
16	chr6:77265160-77265210	AoSMC	blood vessel:	n/a
17	chr6:77265160-77265210	SK-N-MC	brain:	n/a
18	chr6:77265160-77265210	IMR90	lung:	fetal
19	chr6:77265160-77265210	SK-N-SH	brain:	n/a
20	chr6:77265160-77265210	PANC-1	pancreas:	n/a
21	chr6:77265160-77265210	NT2-D1	testis:	n/a
22	chr6:77265160-77265210	HUVEC	blood vessel:	n/a
23	chr6:77265160-77265210	GM19239	blood:	n/a
24	chr6:77265160-77265210	CMK	blood:	n/a
25	chr6:77265160-77265210	SKMC	muscle:	n/a
26	chr6:77265160-77265210	HNPCEpiC	eye:	n/a
27	chr6:77265160-77265210	SAEC	small airway:	n/a
28	chr6:77265160-77265210	ProgFib	skin:	n/a
29	chr6:77265160-77265210	GM06990	blood:	n/a
30	chr6:77265160-77265210	AG04449	skin:	fetal
31	chr6:77265160-77265210	K562	blood:	n/a
32	chr6:77265160-77265210	HCF	heart:	n/a
33	chr6:77265160-77265210	LNCaP	prostate:	n/a
34	chr6:77265160-77265210	Jurkat	blood:	n/a
35	chr6:77265160-77265210	AG10803	skin:	n/a
36	chr6:77265160-77265210	GM12878	blood:	n/a
37	chr6:77265160-77265210	HCM	heart:	n/a
38	chr6:77265160-77265210	HMEC	breast:	n/a
39	chr6:77265160-77265210	Hela-S3	cervix:	n/a
40	chr6:77265160-77265210	AG04450	lung:	fetal
41	chr6:77265160-77265210	HL-60	blood:	n/a
42	chr6:77265160-77265210	NHDF-neo	bronchial:	n/a
43	chr6:77265160-77265210	U87	brain:	n/a
44	chr6:77265160-77265210	MCF10A-Er-Src	breast:	n/a
45	chr6:77265160-77265210	HCPEpiC	choroid plexus:	n/a
46	chr6:77265160-77265210	AG09309	skin:	n/a
47	chr6:77265160-77265210	HRPEpiC	eye:	n/a
48	chr6:77265160-77265210	HAEpiC	amniotic membrane:	n/a
49	chr6:77265160-77265210	HRCEpiC	kidney:	n/a
50	chr6:77265160-77265210	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:
2	chr6:77258609..77260545-chr6:77270279..77272860,2	K562	blood:
3	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:
4	chr6:77172267..77174922-chr6:77177230..77180103,2	K562	blood:
5	chr6:77172267..77174922-chr6:77177230..77180103,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMPG1-1	chr6:77232168-77232521	ENSG00000236635.2
2	lnc-MYO6-2	chr6:77232168-77232521	ENSG00000236635

No data

Variant related genes	Relation type
RNU6-261P	TF binding region
RNU6-261P	CpG island

Extended variants
information (count: 3226 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3226 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187426184	chr6:77130834-77130835	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs192421887	chr6:77130837-77130838	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs73469569	chr6:77130846-77130847	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs112099383	chr6:77130848-77130849	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs112202854	chr6:77130855-77130856	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs555478015	chr6:77130870-77130871	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs567447712	chr6:77130934-77130935	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs138592308	chr6:77130939-77130940	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs553014934	chr6:77131041-77131042	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs577437323	chr6:77131068-77131069	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs538779556	chr6:77131073-77131074	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs9343440	chr6:77131117-77131118	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs575486971	chr6:77131133-77131134	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs529776734	chr6:77131162-77131163	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs111929504	chr6:77131181-77131182	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs560848329	chr6:77131184-77131185	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs367700371	chr6:77131196-77131197	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs567337438	chr6:77131458-77131459	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs560082099	chr6:77131474-77131475	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs534670549	chr6:77131485-77131486	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs183993709	chr6:77131524-77131525	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs113876499	chr6:77131566-77131567	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs138927406	chr6:77131571-77131572	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs74691721	chr6:77131576-77131577	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs142808008	chr6:77131597-77131598	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs113144101	chr6:77131600-77131601	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs73469575	chr6:77131611-77131612	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs541850929	chr6:77131639-77131640	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs9352324	chr6:77131655-77131656	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540192681	chr6:77131659-77131660	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs116891860	chr6:77131681-77131682	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs576866355	chr6:77131691-77131692	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs545300592	chr6:77131760-77131761	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs570624944	chr6:77131777-77131778	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs187853368	chr6:77131790-77131791	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs531515804	chr6:77131796-77131797	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs6903382	chr6:77131798-77131799	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530977977	chr6:77131799-77131800	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs542935709	chr6:77131800-77131801	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs113635843	chr6:77131811-77131812	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs9359197	chr6:77131846-77131847	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192482122	chr6:77131897-77131898	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs139315332	chr6:77131916-77131917	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs561276372	chr6:77131947-77131948	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs6928328	chr6:77131963-77131964	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs35539441	chr6:77131974-77131975	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs386702828	chr6:77131995-77131996	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs6908025	chr6:77131996-77131997	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529495113	chr6:77132025-77132026	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs554910131	chr6:77132039-77132040	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77130800-77131000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
2	chr6:77131000-77131200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
3	chr6:77131400-77131600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
4	chr6:77131400-77131800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
5	chr6:77131800-77132600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
6	chr6:77132000-77133600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr6:77132200-77133000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
8	chr6:77132200-77133000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:77132200-77133400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr6:77132400-77132600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr6:77132400-77132600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:77132400-77133000	Enhancers	Fetal Lung	lung
13	chr6:77132400-77133200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
14	chr6:77132400-77133200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr6:77132600-77134800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:77133000-77133200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
17	chr6:77133800-77134200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr6:77134000-77134200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr6:77134000-77134200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:77134200-77134400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
21	chr6:77135000-77135600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:77135200-77135400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr6:77135200-77135400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:77135200-77135400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr6:77135200-77135400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:77135200-77135600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:77135400-77135600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr6:77140400-77140800	Enhancers	Fetal Lung	lung
29	chr6:77144600-77145200	Enhancers	Adipose Nuclei	Adipose
30	chr6:77144600-77145200	Enhancers	Fetal Heart	heart
31	chr6:77144800-77145200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:77144800-77145200	Enhancers	Brain Hippocampus Middle	brain
33	chr6:77145000-77145200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:77145200-77149200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:77145200-77149200	Weak transcription	Fetal Heart	heart
36	chr6:77145200-77151600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:77148000-77148200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:77148000-77148200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr6:77148000-77148200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:77148200-77149200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr6:77148200-77149400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr6:77148200-77151600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:77148800-77150000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr6:77148800-77152000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:77149000-77149600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr6:77149000-77149800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:77149000-77150200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr6:77149000-77151800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:77149000-77152000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:77149200-77149600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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