Variant report

Variant	nsv916697
Chromosome Location	chr6:66892573-67336786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1033)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:67206650-67206880	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:67199254-67199477	HepG2	liver:	n/a	n/a
3	BCL11A	chr6:66999794-67000063	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr6:66900743-66901106	HepG2	liver:	n/a	n/a
5	BRCA1	chr6:67206671-67206866	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr6:67017402-67017708	K562	blood:	n/a	n/a
7	CCNT2	chr6:67257883-67258083	K562	blood:	n/a	n/a
8	CEBPB	chr6:67146901-67147197	HepG2	liver:	n/a	chr6:67147035-67147046
9	CEBPB	chr6:66952854-66953044	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:66909130-66909176	H1-hESC	embryonic stem cell:	n/a	chr6:66909154-66909167
11	CEBPB	chr6:66947001-66947336	HepG2	liver:	n/a	chr6:66947231-66947240 chr6:66947229-66947240
12	CEBPB	chr6:67199264-67199419	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:67288331-67288563	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:67266780-67267076	HepG2	liver:	n/a	chr6:67266897-67266908
15	CEBPB	chr6:67085285-67085513	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:67178953-67179224	A549	lung:	n/a	chr6:67179113-67179124
17	CEBPB	chr6:66997543-66997824	HepG2	liver:	n/a	chr6:66997640-66997651 chr6:66997661-66997672
18	CEBPB	chr6:67267500-67267729	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:67184681-67184748	H1-hESC	embryonic stem cell:	n/a	chr6:67184700-67184711
20	CEBPB	chr6:67108910-67109181	HepG2	liver:	n/a	chr6:67109030-67109041
21	CEBPB	chr6:67307760-67308057	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:67057762-67058070	HepG2	liver:	n/a	chr6:67057878-67057889
23	CEBPB	chr6:67146882-67147169	IMR90	lung:	n/a	chr6:67147035-67147046
24	CEBPB	chr6:67188587-67188958	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr6:67184554-67184864	HepG2	liver:	n/a	chr6:67184700-67184711
26	CEBPB	chr6:66944777-66944991	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:66976521-66976629	A549	lung:	n/a	n/a
28	CEBPB	chr6:66997596-66997806	IMR90	lung:	n/a	chr6:66997640-66997651 chr6:66997661-66997672
29	CEBPB	chr6:67259668-67259823	HepG2	liver:	n/a	chr6:67259753-67259764 chr6:67259752-67259763 chr6:67259754-67259763
30	CEBPB	chr6:67178940-67179294	HepG2	liver:	n/a	chr6:67179113-67179124
31	CEBPB	chr6:67118289-67118311	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:66953294-66953525	HepG2	liver:	n/a	chr6:66953405-66953416
33	CEBPB	chr6:67253156-67253329	HepG2	liver:	n/a	chr6:67253204-67253215
34	CEBPB	chr6:67178205-67178395	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:67184580-67184880	IMR90	lung:	n/a	chr6:67184700-67184711
36	CEBPZ	chr6:66920925-66921224	HepG2	liver:	n/a	n/a
37	CEBPZ	chr6:67214331-67214383	HepG2	liver:	n/a	n/a
38	CHD2	chr6:67199180-67199449	HepG2	liver:	n/a	n/a
39	CHD2	chr6:67178618-67178639	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr6:67206684-67206832	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:67278220-67278370	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:67031522-67031551	ProgFib	skin:	n/a	n/a
43	CTCF	chr6:67206660-67206810	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr6:67268180-67268330	AG10803	skin:	n/a	n/a
45	CTCF	chr6:67131633-67131710	A549	lung:	n/a	n/a
46	CTCF	chr6:67268300-67268450	GM12871	blood:	n/a	n/a
47	CTCF	chr6:67268160-67268310	GM12864	blood:	n/a	n/a
48	CTCF	chr6:67268280-67268430	GM12869	blood:	n/a	n/a
49	CTCF	chr6:67278280-67278430	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr6:67131611-67131756	Fibrobl	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:67041119-67041169	AG09309	skin:	n/a
2	chr6:67178610-67178660	Jurkat	blood:	n/a
3	chr6:67041119-67041169	A549	lung:	n/a
4	chr6:67041119-67041169	ProgFib	skin:	n/a
5	chr6:67041119-67041169	HepG2	liver:	n/a
6	chr6:67178610-67178660	SKMC	muscle:	n/a
7	chr6:66999374-66999424	PFSK-1	brain:	n/a
8	chr6:67178610-67178660	H1-hESC	embryonic stem cell:	embryo
9	chr6:66999374-66999424	GM12891	blood:	n/a
10	chr6:66999374-66999424	HEK293	kidney:	embryo
11	chr6:67178610-67178660	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:66999374-66999424	HIPEpiC	eye:	n/a
13	chr6:67178610-67178660	NH-A	brain:	n/a
14	chr6:67041119-67041169	SKMC	muscle:	n/a
15	chr6:66999374-66999424	K562	blood:	n/a
16	chr6:66999374-66999424	PrEC	prostate:	n/a
17	chr6:67041119-67041169	PrEC	prostate:	n/a
18	chr6:66999374-66999424	AG04450	lung:	fetal
19	chr6:66999374-66999424	NT2-D1	testis:	n/a
20	chr6:66999374-66999424	HEEpiC	esophagus:	n/a
21	chr6:67041119-67041169	HL-60	blood:	n/a
22	chr6:67041119-67041169	SK-N-MC	brain:	n/a
23	chr6:66999374-66999424	CMK	blood:	n/a
24	chr6:66999374-66999424	ECC-1	luminal epithelium:	n/a
25	chr6:67178610-67178660	HRPEpiC	eye:	n/a
26	chr6:67041119-67041169	MCF10A-Er-Src	breast:	n/a
27	chr6:66999374-66999424	ProgFib	skin:	n/a
28	chr6:67178610-67178660	RPTEC	kidney:	n/a
29	chr6:67178610-67178660	MCF10A-Er-Src	breast:	n/a
30	chr6:67178610-67178660	AG10803	skin:	n/a
31	chr6:67178610-67178660	SK-N-SH	brain:	n/a
32	chr6:66999374-66999424	Caco-2	colon:	n/a
33	chr6:66999374-66999424	NHBE	bronchial:	n/a
34	chr6:66999374-66999424	HMEC	breast:	n/a
35	chr6:66999374-66999424	SAEC	small airway:	n/a
36	chr6:67041119-67041169	GM06990	blood:	n/a
37	chr6:67178610-67178660	CMK	blood:	n/a
38	chr6:66999374-66999424	AG10803	skin:	n/a
39	chr6:67041119-67041169	AG04449	skin:	fetal
40	chr6:67041119-67041169	HAEpiC	amniotic membrane:	n/a
41	chr6:67041119-67041169	GM12891	blood:	n/a
42	chr6:67178610-67178660	PrEC	prostate:	n/a
43	chr6:66999374-66999424	Jurkat	blood:	n/a
44	chr6:67178610-67178660	Hela-S3	cervix:	n/a
45	chr6:66999374-66999424	HCF	heart:	n/a
46	chr6:67178610-67178660	HCF	heart:	n/a
47	chr6:67178610-67178660	GM12892	blood:	n/a
48	chr6:67178610-67178660	LNCaP	prostate:	n/a
49	chr6:67041119-67041169	Caco-2	colon:	n/a
50	chr6:67178610-67178660	AoSMC	blood vessel:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66890023..66892025-chr6:66894680..66896595,2	K562	blood:
2	chr6:67131208..67132075-chr6:67244695..67245464,3	MCF-7	breast:
3	chr6:67131208..67132088-chr6:67206455..67207593,4	MCF-7	breast:
4	chr16:75498580..75499130-chr6:66933180..66934026,2	MCF-7	breast:
5	chr6:67059986..67061952-chr6:67065569..67067514,2	K562	blood:
6	chr6:67008535..67010196-chr6:67047890..67049548,2	MCF-7	breast:
7	chr6:67154196..67156663-chr6:67160167..67162638,2	K562	blood:
8	chr6:67154196..67156663-chr6:67160167..67162638,2	K562	blood:
9	chr6:66890125..66893594-chr6:66896979..66900309,4	MCF-7	breast:
10	chr6:67008535..67010196-chr6:67047890..67049548,2	MCF-7	breast:
11	chr6:67131208..67132088-chr6:67206455..67207593,4	MCF-7	breast:
12	chr6:31794867..31797168-chr6:67137707..67140399,2	MCF-7	breast:
13	chr6:66920773..66922637-chr6:66924312..66926863,2	K562	blood:
14	chr6:66920773..66922637-chr6:66924312..66926863,2	K562	blood:
15	chr6:67059986..67061952-chr6:67065569..67067514,2	K562	blood:
16	chr6:67008436..67009111-chr6:67048434..67049041,2	MCF-7	breast:
17	chr6:67008436..67009111-chr6:67048434..67049041,2	MCF-7	breast:
18	chr6:66890125..66893594-chr6:66896979..66900309,4	MCF-7	breast:
19	chr6:67131208..67132075-chr6:67244695..67245464,3	MCF-7	breast:
20	chr6:67240333..67242472-chrX:106418338..106419890,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000221281	TF binding region
ENSG00000221281	CpG island
ENSG00000261717	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000204388	chromatin interactions

Extended variants
information (count: 4352 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4352 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187201207	chr6:66892576-66892577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573571763	chr6:66892634-66892635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547070834	chr6:66892642-66892643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566881483	chr6:66892643-66892644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192807564	chr6:66892705-66892706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549436633	chr6:66892721-66892722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138090565	chr6:66892801-66892802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112725608	chr6:66892802-66892803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs67131916	chr6:66892803-66892804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs57576940	chr6:66892804-66892805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371110876	chr6:66892805-66892806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373285493	chr6:66892808-66892809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376593467	chr6:66892809-66892810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370788022	chr6:66892810-66892811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569513172	chr6:66892817-66892818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538092531	chr6:66892818-66892819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557924766	chr6:66892821-66892822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528697849	chr6:66892823-66892824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571459327	chr6:66892886-66892887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539152681	chr6:66892890-66892891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549354631	chr6:66892898-66892899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549282407	chr6:66892899-66892900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9453616	chr6:66892903-66892904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572771613	chr6:66892938-66892939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541787978	chr6:66893036-66893037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555407045	chr6:66893041-66893042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575484975	chr6:66893102-66893103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544466768	chr6:66893124-66893125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564278245	chr6:66893130-66893131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146587762	chr6:66893138-66893139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141287060	chr6:66893186-66893187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560610145	chr6:66893260-66893261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1418854	chr6:66893284-66893285	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549346010	chr6:66893295-66893296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569492706	chr6:66893297-66893298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150205173	chr6:66893361-66893362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372099465	chr6:66893393-66893394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531015549	chr6:66893499-66893500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551614784	chr6:66893511-66893512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7762308	chr6:66893552-66893553	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185479670	chr6:66893574-66893575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552677583	chr6:66893582-66893583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190351323	chr6:66893609-66893610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535145985	chr6:66893680-66893681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs851599	chr6:66893737-66893738	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs851600	chr6:66893754-66893755	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182529399	chr6:66893755-66893756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558051668	chr6:66893804-66893805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577935271	chr6:66893816-66893817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183567274	chr6:66893845-66893846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19214233	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Autism	19287141	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66888800-66893400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:66890000-66892800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:66892800-66895400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:66893000-66893400	Enhancers	NHDF-Ad	bronchial
5	chr6:66893200-66894200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:66893400-66894200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:66893400-66894600	Weak transcription	NHDF-Ad	bronchial
8	chr6:66893800-66895000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr6:66894000-66894800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:66894200-66894600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:66894200-66894600	Enhancers	Brain Hippocampus Middle	brain
12	chr6:66894200-66894800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:66894200-66895200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:66894600-66895000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:66894600-66895200	Enhancers	NHDF-Ad	bronchial
16	chr6:66894800-66895200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:66894800-66896400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:66895000-66896000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:66895200-66896200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:66895400-66895800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:66895800-66896600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:66896000-66897200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr6:66896200-66896400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:66896400-66896600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:66896400-66897400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:66897400-66898000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:66897400-66900600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:66897800-66898800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr6:66899800-66901400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:66900000-66901400	Enhancers	HepG2	liver
31	chr6:66900600-66901000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:66900600-66901200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:66900800-66901200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:66900800-66901600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:66907200-66909400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:66907200-66910600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:66909200-66909600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:66909200-66909600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:66909200-66910400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr6:66909600-66910000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:66909600-66910400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:66910000-66910200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:66910200-66911400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:66910400-66911600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:66911400-66911600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:66918600-66919000	ZNF genes & repeats	Aorta	Aorta
47	chr6:66935200-66935400	Enhancers	Gastric	stomach
48	chr6:66935600-66936800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr6:66935800-66936200	Enhancers	Brain Germinal Matrix	brain
50	chr6:66935800-66936200	Enhancers	Fetal Heart	heart

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