Variant report

Variant	nsv1020246
Chromosome Location	chr6:66413907-66536897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:491)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 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	BCL3	chr6:66528842-66529413	A549	lung:	n/a	n/a
2	CEBPB	chr6:66439123-66439443	HepG2	liver:	n/a	chr6:66439271-66439280 chr6:66439269-66439282 chr6:66439269-66439280
3	CEBPB	chr6:66528925-66529488	A549	lung:	n/a	n/a
4	CEBPB	chr6:66529301-66529561	A549	lung:	n/a	n/a
5	CEBPB	chr6:66490682-66491041	A549	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
6	CEBPB	chr6:66516355-66516697	HepG2	liver:	n/a	chr6:66516524-66516535
7	CEBPB	chr6:66490602-66490966	IMR90	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
8	CEBPB	chr6:66516356-66516600	A549	lung:	n/a	chr6:66516524-66516535
9	CEBPB	chr6:66490621-66490964	K562	blood:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
10	CEBPB	chr6:66490661-66490950	H1-hESC	embryonic stem cell:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
11	CEBPB	chr6:66490606-66490975	HepG2	liver:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
12	CEBPB	chr6:66490610-66490962	A549	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
13	CEBPB	chr6:66516368-66516688	IMR90	lung:	n/a	chr6:66516524-66516535
14	CHD2	chr6:66486288-66486596	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:66504680-66504830	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:66486366-66486522	HepG2	liver:	n/a	n/a
17	CTCF	chr6:66456418-66456456	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr6:66454700-66454850	GM12869	blood:	n/a	n/a
19	CTCF	chr6:66504566-66504833	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:66486419-66486467	GM12878	blood:	n/a	n/a
21	CTCF	chr6:66504625-66504805	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:66458285-66458323	GM10248	blood:	n/a	n/a
23	CTCF	chr6:66486360-66486510	SAEC	small airway:	n/a	n/a
24	CTCF	chr6:66504639-66504784	Fibrobl	skin:	n/a	n/a
25	CTCF	chr6:66486324-66486562	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:66486260-66486410	RPTEC	kidney:	n/a	n/a
27	CTCF	chr6:66504554-66504853	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:66486350-66486499	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr6:66504547-66504840	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:66486360-66486510	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr6:66486297-66486582	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:66504593-66504795	Gliobla	brain:	n/a	n/a
33	CTCF	chr6:66486393-66486533	LNCaP	prostate:	n/a	n/a
34	CTCF	chr6:66486400-66486550	BE2_C	brain:	n/a	n/a
35	CTCF	chr6:66486419-66486547	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:66486340-66486490	HPF	lung:	n/a	n/a
37	CTCF	chr6:66486236-66486624	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:66456367-66456400	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:66486320-66486470	HPF	lung:	n/a	n/a
40	CTCF	chr6:66486360-66486510	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr6:66486381-66486520	ProgFib	skin:	n/a	n/a
42	CTCF	chr6:66486226-66486627	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:66486361-66486536	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr6:66504560-66504710	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:66486413-66486472	K562	blood:	n/a	n/a
46	CTCF	chr6:66486380-66486503	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:66486339-66486561	HepG2	liver:	n/a	n/a
48	CTCF	chr6:66529260-66529410	A549	lung:	n/a	n/a
49	CTCF	chr6:66486436-66486484	Fibrobl	skin:	n/a	n/a
50	CTCF	chr6:66457784-66457814	GM13976	blood:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66493769-66493819	ProgFib	skin:	n/a
2	chr6:66498032-66498082	NHDF-neo	bronchial:	n/a
3	chr6:66493769-66493819	NH-A	brain:	n/a
4	chr6:66493769-66493819	ProgFib	skin:	n/a
5	chr6:66498032-66498082	NHDF-neo	bronchial:	n/a
6	chr6:66493769-66493819	NH-A	brain:	n/a
7	chr6:66493769-66493819	GM12878	blood:	n/a
8	chr6:66496955-66497005	RPTEC	kidney:	n/a
9	chr6:66497746-66497796	A549	lung:	n/a
10	chr6:66498734-66498784	K562	blood:	n/a
11	chr6:66498734-66498784	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:66493769-66493819	Jurkat	blood:	n/a
13	chr6:66496955-66497005	K562	blood:	n/a
14	chr6:66498734-66498784	Jurkat	blood:	n/a
15	chr6:66497586-66497636	Jurkat	blood:	n/a
16	chr6:66493769-66493819	Caco-2	colon:	n/a
17	chr6:66496346-66496396	HAEpiC	amniotic membrane:	n/a
18	chr6:66497586-66497636	K562	blood:	n/a
19	chr6:66496346-66496396	HNPCEpiC	eye:	n/a
20	chr6:66498032-66498082	AoSMC	blood vessel:	n/a
21	chr6:66497586-66497636	NB4	blood:	n/a
22	chr6:66497885-66497935	HMEC	breast:	n/a
23	chr6:66497885-66497935	NHBE	bronchial:	n/a
24	chr6:66498734-66498784	HIPEpiC	eye:	n/a
25	chr6:66496955-66497005	GM12892	blood:	n/a
26	chr6:66498032-66498082	HNPCEpiC	eye:	n/a
27	chr6:66496955-66497005	HAEpiC	amniotic membrane:	n/a
28	chr6:66497586-66497636	BJ	skin:	n/a
29	chr6:66498032-66498082	SKMC	muscle:	n/a
30	chr6:66496346-66496396	MCF10A-Er-Src	breast:	n/a
31	chr6:66498032-66498082	RPTEC	kidney:	n/a
32	chr6:66497746-66497796	Hepatocyte	liver:	n/a
33	chr6:66497885-66497935	GM12878	blood:	n/a
34	chr6:66498032-66498082	HEEpiC	esophagus:	n/a
35	chr6:66496346-66496396	SK-N-SH	brain:	n/a
36	chr6:66497746-66497796	AG04449	skin:	fetal
37	chr6:66498734-66498784	GM12892	blood:	n/a
38	chr6:66497885-66497935	HIPEpiC	eye:	n/a
39	chr6:66497586-66497636	HAEpiC	amniotic membrane:	n/a
40	chr6:66497885-66497935	PFSK-1	brain:	n/a
41	chr6:66496346-66496396	ProgFib	skin:	n/a
42	chr6:66496955-66497005	AG04450	lung:	fetal
43	chr6:66497746-66497796	SK-N-MC	brain:	n/a
44	chr6:66493769-66493819	NHBE	bronchial:	n/a
45	chr6:66497586-66497636	H1-hESC	embryonic stem cell:	embryo
46	chr6:66498734-66498784	AG10803	skin:	n/a
47	chr6:66497746-66497796	NT2-D1	testis:	n/a
48	chr6:66497885-66497935	HCPEpiC	choroid plexus:	n/a
49	chr6:66497885-66497935	A549	lung:	n/a
50	chr6:66497586-66497636	RPTEC	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
2	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:
3	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:
4	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:
5	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
6	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGSN-7	chr6:66417028-66417107	NONHSAT113373

No data

Variant related genes	Relation type
SLC25A51P1	TF binding region
EYS	TF binding region
SLC25A51P1	CpG island
EYS	CpG island

Extended variants
information (count: 937 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183464082	chr6:66413918-66413919	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571916705	chr6:66413920-66413921	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376818195	chr6:66413944-66413945	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369377718	chr6:66414032-66414033	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115218579	chr6:66414079-66414080	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561269749	chr6:66414102-66414103	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79523120	chr6:66414139-66414140	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543486077	chr6:66414142-66414143	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114250312	chr6:66414146-66414147	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534023697	chr6:66414153-66414154	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532825492	chr6:66414173-66414174	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs996929	chr6:66414226-66414227	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559977329	chr6:66414245-66414246	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528743040	chr6:66414268-66414269	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145393703	chr6:66414281-66414282	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567285125	chr6:66414388-66414389	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145187365	chr6:66414391-66414392	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149119315	chr6:66414432-66414433	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569639220	chr6:66414442-66414443	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117763801	chr6:66414451-66414452	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552586147	chr6:66414460-66414461	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564275620	chr6:66414461-66414462	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538508077	chr6:66414500-66414501	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558460138	chr6:66414503-66414504	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571904358	chr6:66414530-66414531	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532039308	chr6:66414531-66414532	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555605412	chr6:66414538-66414539	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534534155	chr6:66414545-66414546	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550245320	chr6:66414623-66414624	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568407995	chr6:66414630-66414631	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142205516	chr6:66414643-66414644	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115029029	chr6:66414656-66414657	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151199921	chr6:66414682-66414683	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563487388	chr6:66414703-66414704	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187322095	chr6:66414735-66414736	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546517444	chr6:66414789-66414790	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12526729	chr6:66414828-66414829	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs528683423	chr6:66414833-66414834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548462199	chr6:66414906-66414907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562331834	chr6:66414948-66414949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529711618	chr6:66414961-66414962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549860862	chr6:66414973-66414974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114141712	chr6:66415015-66415016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114683410	chr6:66415019-66415020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140320563	chr6:66415058-66415059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190967473	chr6:66415095-66415096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565670375	chr6:66415180-66415181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116502113	chr6:66415207-66415208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116024718	chr6:66415216-66415217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574577661	chr6:66415236-66415237	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	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
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Retinitis pigmentosa	21519034	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66413800-66414000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:66413800-66414800	Enhancers	A549	lung
3	chr6:66414000-66414400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr6:66414400-66414800	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr6:66414800-66415200	Weak transcription	A549	lung
6	chr6:66414800-66415400	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:66415000-66415200	Enhancers	Fetal Intestine Small	intestine
8	chr6:66415000-66415600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:66415200-66415400	Enhancers	A549	lung
10	chr6:66415400-66416400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:66415400-66416400	Weak transcription	A549	lung
12	chr6:66415600-66416400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:66415600-66416600	Weak transcription	Fetal Intestine Small	intestine
14	chr6:66416200-66416400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:66416400-66416600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr6:66416400-66416800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:66416400-66416800	Enhancers	A549	lung
18	chr6:66416400-66417400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:66416400-66418400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:66416600-66417000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr6:66416600-66417200	Enhancers	Fetal Intestine Small	intestine
22	chr6:66416800-66418400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:66417000-66417200	Enhancers	Fetal Brain Male	brain
24	chr6:66417000-66417400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:66417000-66417400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:66417000-66417400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:66417000-66417400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr6:66417000-66417600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr6:66417000-66417800	Enhancers	Fetal Brain Female	brain
30	chr6:66417200-66418200	Weak transcription	Fetal Brain Male	brain
31	chr6:66417600-66418200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr6:66418200-66418600	Enhancers	Fetal Brain Male	brain
33	chr6:66418800-66419000	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr6:66438600-66439000	Enhancers	Fetal Intestine Large	intestine
35	chr6:66438600-66439400	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr6:66438800-66439200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:66456200-66456600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:66470200-66470600	Enhancers	A549	lung
39	chr6:66470200-66471000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:66470200-66473000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:66475000-66475200	Bivalent Enhancer	Fetal Heart	heart
42	chr6:66475200-66477800	Enhancers	Fetal Heart	heart
43	chr6:66476400-66476600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:66479000-66479200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr6:66481600-66482200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr6:66481600-66482200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:66481800-66482000	Enhancers	Gastric	stomach
48	chr6:66481800-66482200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:66482000-66482400	ZNF genes & repeats	Gastric	stomach
50	chr6:66483800-66484600	Enhancers	Fetal Heart	heart

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