Variant report

Variant	nsv1026054
Chromosome Location	chr6:77294100-77479689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:867)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:77392631-77392819	HepG2	liver:	n/a	n/a
2	ATF2	chr6:77394560-77394995	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:77343096-77343299	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:77327841-77327855	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:77452711-77452954	GM12878	blood:	n/a	chr6:77452825-77452836 chr6:77452785-77452796 chr6:77452811-77452822
6	CCNT2	chr6:77478292-77478511	K562	blood:	n/a	n/a
7	CEBPB	chr6:77413553-77413907	HepG2	liver:	n/a	chr6:77413730-77413741
8	CEBPB	chr6:77376602-77376713	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:77413504-77413930	H1-hESC	embryonic stem cell:	n/a	chr6:77413730-77413741
10	CEBPB	chr6:77413553-77413888	A549	lung:	n/a	chr6:77413730-77413741
11	CEBPB	chr6:77413546-77413932	Hela-S3	cervix:	n/a	chr6:77413730-77413741
12	CEBPB	chr6:77413535-77413938	ECC-1	luminal epithelium:	n/a	chr6:77413730-77413741
13	CEBPB	chr6:77407299-77407645	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:77330548-77330824	K562	blood:	n/a	chr6:77330676-77330687
15	CEBPB	chr6:77330501-77330855	HepG2	liver:	n/a	chr6:77330676-77330687
16	CEBPB	chr6:77413524-77413879	A549	lung:	n/a	chr6:77413730-77413741
17	CEBPB	chr6:77407362-77407722	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:77413548-77413922	IMR90	lung:	n/a	chr6:77413730-77413741
19	CEBPB	chr6:77413578-77413961	MCF-7	breast:	n/a	chr6:77413730-77413741
20	CEBPB	chr6:77330433-77330828	H1-hESC	embryonic stem cell:	n/a	chr6:77330676-77330687
21	CEBPB	chr6:77413576-77413932	ECC-1	luminal epithelium:	n/a	chr6:77413730-77413741
22	CEBPB	chr6:77413509-77413912	MCF-7	breast:	n/a	chr6:77413730-77413741
23	CEBPB	chr6:77436454-77436764	A549	lung:	n/a	n/a
24	CEBPB	chr6:77303904-77304153	HepG2	liver:	n/a	chr6:77304017-77304028
25	CEBPB	chr6:77330504-77330849	IMR90	lung:	n/a	chr6:77330676-77330687
26	CHD1	chr6:77294414-77294455	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr6:77303098-77303102	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:77306735-77306899	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr6:77394680-77394830	BJ	skin:	n/a	n/a
30	CTCF	chr6:77400739-77401119	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:77392660-77392810	HMEC	breast:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
32	CTCF	chr6:77392580-77392730	RPTEC	kidney:	n/a	n/a
33	CTCF	chr6:77343040-77343190	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr6:77392640-77392790	AG04450	lung:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
35	CTCF	chr6:77407380-77407530	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr6:77392640-77392790	AG04449	skin:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
37	CTCF	chr6:77411360-77411510	HAc	cerebellar:	n/a	n/a
38	CTCF	chr6:77418440-77418590	WI-38	lung:	n/a	n/a
39	CTCF	chr6:77418560-77418710	NHLF	lung:	n/a	n/a
40	CTCF	chr6:77392660-77392810	GM12866	blood:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
41	CTCF	chr6:77343120-77343270	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:77392600-77392750	NHEK	skin:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
43	CTCF	chr6:77407420-77407570	HEK293	kidney:	n/a	chr6:77407536-77407546
44	CTCF	chr6:77411440-77411590	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr6:77418400-77418550	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr6:77325259-77325398	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:77392700-77392850	GM12871	blood:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
48	CTCF	chr6:77418400-77418550	AG04450	lung:	n/a	n/a
49	CTCF	chr6:77392660-77392810	HCFaa	heart:	n/a	chr6:77392725-77392746 chr6:77392724-77392740 chr6:77392723-77392741
50	CTCF	chr6:77418380-77418530	AG09319	gingival:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:77322589-77322639	HAEpiC	amniotic membrane:	n/a
2	chr6:77394161-77394211	SKMC	muscle:	n/a
3	chr6:77394161-77394211	SK-N-SH_RA	brain:	n/a
4	chr6:77322589-77322639	Caco-2	colon:	n/a
5	chr6:77322589-77322639	SK-N-SH_RA	brain:	n/a
6	chr6:77322589-77322639	LNCaP	prostate:	n/a
7	chr6:77322589-77322639	HIPEpiC	eye:	n/a
8	chr6:77322589-77322639	HL-60	blood:	n/a
9	chr6:77394161-77394211	A549	lung:	n/a
10	chr6:77394161-77394211	HCF	heart:	n/a
11	chr6:77322589-77322639	HRPEpiC	eye:	n/a
12	chr6:77322589-77322639	GM12892	blood:	n/a
13	chr6:77394161-77394211	HNPCEpiC	eye:	n/a
14	chr6:77394161-77394211	NHBE	bronchial:	n/a
15	chr6:77322589-77322639	NT2-D1	testis:	n/a
16	chr6:77322589-77322639	AG04450	lung:	fetal
17	chr6:77322589-77322639	GM12891	blood:	n/a
18	chr6:77394161-77394211	MCF-7	breast:	n/a
19	chr6:77322589-77322639	HCT-116	colon:	n/a
20	chr6:77394161-77394211	HAEpiC	amniotic membrane:	n/a
21	chr6:77322589-77322639	HUVEC	blood vessel:	n/a
22	chr6:77394161-77394211	HL-60	blood:	n/a
23	chr6:77322589-77322639	HNPCEpiC	eye:	n/a
24	chr6:77322589-77322639	T-47D	breast:	n/a
25	chr6:77322589-77322639	SK-N-MC	brain:	n/a
26	chr6:77394161-77394211	ovcar-3	ovarian:	n/a
27	chr6:77394161-77394211	H1-hESC	embryonic stem cell:	embryo
28	chr6:77394161-77394211	HRPEpiC	eye:	n/a
29	chr6:77322589-77322639	NHBE	bronchial:	n/a
30	chr6:77394161-77394211	SK-N-SH	brain:	n/a
31	chr6:77394161-77394211	U87	brain:	n/a
32	chr6:77322589-77322639	IMR90	lung:	fetal
33	chr6:77322589-77322639	H1-hESC	embryonic stem cell:	embryo
34	chr6:77394161-77394211	K562	blood:	n/a
35	chr6:77322589-77322639	GM06990	blood:	n/a
36	chr6:77394161-77394211	LNCaP	prostate:	n/a
37	chr6:77394161-77394211	HRE	kidney:	n/a
38	chr6:77394161-77394211	ECC-1	luminal epithelium:	n/a
39	chr6:77394161-77394211	PrEC	prostate:	n/a
40	chr6:77322589-77322639	NHDF-neo	bronchial:	n/a
41	chr6:77322589-77322639	Jurkat	blood:	n/a
42	chr6:77322589-77322639	K562	blood:	n/a
43	chr6:77394161-77394211	BE2_C	brain:	n/a
44	chr6:77322589-77322639	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:77322589-77322639	NB4	blood:	n/a
46	chr6:77394161-77394211	SK-N-MC	brain:	n/a
47	chr6:77394161-77394211	HEK293	kidney:	embryo
48	chr6:77394161-77394211	HIPEpiC	eye:	n/a
49	chr6:77394161-77394211	GM12892	blood:	n/a
50	chr6:77322589-77322639	AG10803	skin:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:77392645..77395103-chr6:77585280..77587587,2	MCF-7	breast:
2	chr6:77464445..77465326-chr7:1518971..1519642,2	MCF-7	breast:
3	chr6:77418110..77418947-chr6:77570902..77571718,2	MCF-7	breast:
4	chr1:11967926..11968691-chr6:77296332..77297332,3	Hela-S3	cervix:
5	chr6:77420178..77422936-chr6:77426529..77430097,4	MCF-7	breast:
6	chr6:77355946..77358313-chr6:77365229..77366836,2	K562	blood:
7	chr6:77407151..77408023-chr6:77621937..77622579,2	MCF-7	breast:
8	chr6:77406988..77407870-chr6:77586545..77587424,2	MCF-7	breast:
9	chr6:77420178..77422936-chr6:77426529..77430097,4	MCF-7	breast:
10	chr6:77407039..77407928-chr6:77570847..77571390,2	MCF-7	breast:
11	chr6:77355946..77358313-chr6:77365229..77366836,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMPG1-1	chr6:77296165-77296283	ENSG00000236635.2
2	lnc-MYO6-9	chr6:77370203-77372487	NONHSAT113645
3	lnc-MYO6-8	chr6:77359965-77360059	NONHSAT113643
4	lnc-MYO6-2	chr6:77303246-77303340	ENSG00000236635
5	lnc-MYO6-8	chr6:77352885-77353004	NONHSAT113643
6	lnc-IMPG1-1	chr6:77303244-77303340	ENSG00000236635.2
7	lnc-MYO6-2	chr6:77296178-77296285	XLOC_005354
8	lnc-MYO6-2	chr6:77303246-77303510	XLOC_005354
9	lnc-MYO6-2	chr6:77296166-77296285	ENSG00000236635

No data

Variant related genes	Relation type
ENSG00000231762	TF binding region
ENSG00000236635	TF binding region
ENSG00000231762	CpG island
ENSG00000236635	CpG island
ENSG00000199347	chromatin interactions
JAK1	miRNA target sites

Extended variants
information (count: 5820 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:5820 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190080032	chr6:77294132-77294133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539873895	chr6:77294180-77294181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557978377	chr6:77294188-77294189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570180669	chr6:77294190-77294191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537421343	chr6:77294242-77294243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555832531	chr6:77294248-77294249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143683090	chr6:77294266-77294267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553088080	chr6:77294280-77294281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs118164353	chr6:77294308-77294309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545227563	chr6:77294349-77294350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563232253	chr6:77294367-77294368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530545988	chr6:77294449-77294450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370838833	chr6:77294501-77294502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542198041	chr6:77294516-77294517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556664340	chr6:77294530-77294531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529515687	chr6:77294546-77294547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547775707	chr6:77294677-77294678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535845218	chr6:77294679-77294680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192910366	chr6:77294736-77294737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185585150	chr6:77294770-77294771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548040396	chr6:77294779-77294780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146800611	chr6:77294804-77294805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570149258	chr6:77294852-77294853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537558286	chr6:77294858-77294859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555773216	chr6:77294874-77294875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189538218	chr6:77294881-77294882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566469973	chr6:77294893-77294894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180811983	chr6:77294896-77294897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79430653	chr6:77294919-77294920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140421072	chr6:77294936-77294937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185431407	chr6:77295011-77295012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150485323	chr6:77295019-77295020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188631780	chr6:77295026-77295027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542334682	chr6:77295077-77295078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578023557	chr6:77295236-77295237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375447894	chr6:77295267-77295268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181115662	chr6:77295275-77295276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145388386	chr6:77295277-77295278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186348164	chr6:77295293-77295294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559775747	chr6:77295297-77295298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533716460	chr6:77295333-77295334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10943371	chr6:77295335-77295336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs112814121	chr6:77295359-77295360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557196587	chr6:77295370-77295371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570285994	chr6:77295379-77295380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371788798	chr6:77295385-77295386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540625601	chr6:77295387-77295388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553947985	chr6:77295402-77295403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549511078	chr6:77295408-77295409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117468813	chr6:77295435-77295436	Weak transcription	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77284600-77303000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:77285200-77302000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:77285800-77301400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:77288600-77302000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:77288800-77303400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:77289000-77303600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:77293800-77294400	Enhancers	Fetal Heart	heart
8	chr6:77296800-77298000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:77297200-77297800	Enhancers	HUVEC	blood vessel
10	chr6:77297800-77302000	Weak transcription	HUVEC	blood vessel
11	chr6:77301400-77302400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:77302000-77302400	Enhancers	HUVEC	blood vessel
13	chr6:77302000-77304400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr6:77302000-77309000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr6:77302400-77306400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:77303000-77304000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:77303000-77304200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr6:77303000-77304200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr6:77303000-77304400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr6:77303400-77304200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:77303600-77304200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
22	chr6:77305400-77305600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr6:77306200-77306800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr6:77306400-77306800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:77316800-77322400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:77318600-77318800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:77318800-77319000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:77318800-77319200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:77319000-77320200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:77319000-77320800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:77319200-77319400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:77319400-77326200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:77320200-77320400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr6:77320800-77321000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr6:77321000-77321400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr6:77321400-77322400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr6:77321400-77323200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:77321600-77322200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:77322200-77322600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:77322200-77323200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr6:77322200-77323400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:77322200-77323400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr6:77322400-77322800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:77322400-77323000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:77322400-77323000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr6:77322400-77323200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr6:77322600-77322800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:77322600-77323200	Enhancers	H9 Cell Line	embryonic stem cell
49	chr6:77322600-77323200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:77322800-77323200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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