Variant report

Variant	nsv538307
Chromosome Location	chr6:74776830-74907758
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:74801147-74801533	HepG2	liver:	n/a	n/a
2	BHLHE40	chr6:74892790-74893173	HepG2	liver:	n/a	n/a
3	CBX3	chr6:74847549-74848161	HCT-116	colon:	n/a	n/a
4	CBX3	chr6:74801110-74801569	HCT-116	colon:	n/a	n/a
5	CCNT2	chr6:74827126-74827221	K562	blood:	n/a	n/a
6	CEBPB	chr6:74847685-74848113	IMR90	lung:	n/a	chr6:74847919-74847930
7	CEBPB	chr6:74847710-74848056	ECC-1	luminal epithelium:	n/a	chr6:74847919-74847930
8	CEBPB	chr6:74825464-74825811	IMR90	lung:	n/a	chr6:74825621-74825632
9	CEBPB	chr6:74847515-74848240	HCT-116	colon:	n/a	chr6:74847919-74847930
10	CEBPB	chr6:74825498-74825731	H1-hESC	embryonic stem cell:	n/a	chr6:74825621-74825632
11	CEBPB	chr6:74823654-74823896	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:74824402-74824708	IMR90	lung:	n/a	n/a
13	CEBPB	chr6:74811442-74811617	IMR90	lung:	n/a	n/a
14	CEBPB	chr6:74871158-74871550	HCT-116	colon:	n/a	chr6:74871272-74871283
15	CEBPB	chr6:74825462-74825784	HepG2	liver:	n/a	chr6:74825621-74825632
16	CEBPB	chr6:74847732-74848101	H1-hESC	embryonic stem cell:	n/a	chr6:74847919-74847930
17	CEBPB	chr6:74785099-74785398	Hela-S3	cervix:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
18	CEBPB	chr6:74783207-74783464	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:74887967-74888079	HepG2	liver:	n/a	chr6:74888034-74888045 chr6:74888034-74888047
20	CEBPB	chr6:74871121-74871482	Hela-S3	cervix:	n/a	chr6:74871272-74871283
21	CEBPB	chr6:74879906-74880271	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:74790615-74790619	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:74786135-74786343	A549	lung:	n/a	chr6:74786167-74786179 chr6:74786208-74786219 chr6:74786206-74786219 chr6:74786206-74786217
24	CEBPB	chr6:74833368-74833645	HepG2	liver:	n/a	chr6:74833523-74833534
25	CEBPB	chr6:74795063-74795245	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:74786155-74786301	HepG2	liver:	n/a	chr6:74786167-74786179 chr6:74786208-74786219 chr6:74786206-74786219 chr6:74786206-74786217
27	CEBPB	chr6:74825477-74825842	MCF-7	breast:	n/a	chr6:74825621-74825632
28	CEBPB	chr6:74785109-74785309	A549	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
29	CEBPB	chr6:74825484-74825838	ECC-1	luminal epithelium:	n/a	chr6:74825621-74825632
30	CEBPB	chr6:74847773-74848061	A549	lung:	n/a	chr6:74847919-74847930
31	CEBPB	chr6:74847743-74848092	HepG2	liver:	n/a	chr6:74847919-74847930
32	CEBPB	chr6:74833341-74833624	MCF-7	breast:	n/a	chr6:74833523-74833534
33	CEBPB	chr6:74847592-74848136	Hela-S3	cervix:	n/a	chr6:74847919-74847930
34	CEBPB	chr6:74838360-74838570	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:74825460-74825833	ECC-1	luminal epithelium:	n/a	chr6:74825621-74825632
36	CEBPB	chr6:74847635-74848230	HCT-116	colon:	n/a	chr6:74847919-74847930
37	CEBPB	chr6:74895544-74895656	A549	lung:	n/a	chr6:74895619-74895630 chr6:74895617-74895630
38	CEBPB	chr6:74784948-74785495	HCT-116	colon:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
39	CEBPB	chr6:74785098-74785334	H1-hESC	embryonic stem cell:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
40	CEBPB	chr6:74785083-74785369	IMR90	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
41	CEBPB	chr6:74825459-74825797	Hela-S3	cervix:	n/a	chr6:74825621-74825632
42	CEBPB	chr6:74779883-74780137	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:74785096-74785355	HepG2	liver:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
44	CEBPB	chr6:74847743-74848121	MCF-7	breast:	n/a	chr6:74847919-74847930
45	CEBPB	chr6:74825487-74825753	A549	lung:	n/a	chr6:74825621-74825632
46	CEBPB	chr6:74871121-74871432	IMR90	lung:	n/a	chr6:74871272-74871283
47	CEBPB	chr6:74871207-74871361	K562	blood:	n/a	chr6:74871272-74871283
48	CEBPB	chr6:74785013-74785395	HCT-116	colon:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
49	CEBPB	chr6:74871166-74871418	HepG2	liver:	n/a	chr6:74871272-74871283
50	CEBPB	chr6:74871176-74871509	HCT-116	colon:	n/a	chr6:74871272-74871283

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74778313-74778363	BE2_C	brain:	n/a
2	chr6:74784340-74784390	A549	lung:	n/a
3	chr6:74778313-74778363	HNPCEpiC	eye:	n/a
4	chr6:74826447-74826497	MCF10A-Er-Src	breast:	n/a
5	chr6:74826447-74826497	HCM	heart:	n/a
6	chr6:74826447-74826497	SK-N-SH_RA	brain:	n/a
7	chr6:74784340-74784390	HCPEpiC	choroid plexus:	n/a
8	chr6:74778945-74778995	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:74784340-74784390	SK-N-SH_RA	brain:	n/a
10	chr6:74784340-74784390	HepG2	liver:	n/a
11	chr6:74801378-74801428	GM12892	blood:	n/a
12	chr6:74801378-74801428	HMEC	breast:	n/a
13	chr6:74778313-74778363	HIPEpiC	eye:	n/a
14	chr6:74877005-74877055	HIPEpiC	eye:	n/a
15	chr6:74877005-74877055	HRCEpiC	kidney:	n/a
16	chr6:74877005-74877055	ovcar-3	ovarian:	n/a
17	chr6:74877005-74877055	Hela-S3	cervix:	n/a
18	chr6:74877005-74877055	LNCaP	prostate:	n/a
19	chr6:74801378-74801428	HL-60	blood:	n/a
20	chr6:74801378-74801428	BJ	skin:	n/a
21	chr6:74801378-74801428	HUVEC	blood vessel:	n/a
22	chr6:74877005-74877055	A549	lung:	n/a
23	chr6:74778313-74778363	Jurkat	blood:	n/a
24	chr6:74877005-74877055	NT2-D1	testis:	n/a
25	chr6:74877005-74877055	AG09309	skin:	n/a
26	chr6:74801378-74801428	HNPCEpiC	eye:	n/a
27	chr6:74877005-74877055	RPTEC	kidney:	n/a
28	chr6:74826447-74826497	HL-60	blood:	n/a
29	chr6:74826447-74826497	AG09319	gingival:	n/a
30	chr6:74778945-74778995	HEEpiC	esophagus:	n/a
31	chr6:74826447-74826497	AG04449	skin:	fetal
32	chr6:74877005-74877055	HEK293	kidney:	embryo
33	chr6:74801378-74801428	HCT-116	colon:	n/a
34	chr6:74826447-74826497	HCT-116	colon:	n/a
35	chr6:74801378-74801428	U87	brain:	n/a
36	chr6:74877005-74877055	HepG2	liver:	n/a
37	chr6:74778313-74778363	PANC-1	pancreas:	n/a
38	chr6:74801378-74801428	MCF-7	breast:	n/a
39	chr6:74778945-74778995	PANC-1	pancreas:	n/a
40	chr6:74877005-74877055	IMR90	lung:	fetal
41	chr6:74784340-74784390	K562	blood:	n/a
42	chr6:74778313-74778363	GM19239	blood:	n/a
43	chr6:74826447-74826497	Caco-2	colon:	n/a
44	chr6:74826447-74826497	GM12891	blood:	n/a
45	chr6:74784340-74784390	HRPEpiC	eye:	n/a
46	chr6:74826447-74826497	ECC-1	luminal epithelium:	n/a
47	chr6:74826447-74826497	A549	lung:	n/a
48	chr6:74801378-74801428	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:74778945-74778995	ovcar-3	ovarian:	n/a
50	chr6:74826447-74826497	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:74892709..74895952-chr6:74900506..74904423,4	K562	blood:
2	chr6:74815697..74817712-chr6:74819517..74822083,2	K562	blood:
3	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:
4	chr6:74812681..74814220-chr6:74816370..74818420,2	K562	blood:
5	chr6:74892709..74895952-chr6:74900506..74904423,4	K562	blood:
6	chr6:74815697..74817712-chr6:74819517..74822083,2	K562	blood:
7	chr6:74564800..74565363-chr6:74797356..74797902,2	MCF-7	breast:
8	chr6:74870023..74872617-chr6:74890173..74892829,2	MCF-7	breast:
9	chr6:74564799..74565392-chr6:74801154..74801695,2	MCF-7	breast:
10	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:
11	chr6:74870023..74872617-chr6:74890173..74892829,2	MCF-7	breast:
12	chr6:74812681..74814220-chr6:74816370..74818420,2	K562	blood:
13	chr6:74835506..74837786-chr6:74837930..74840707,2	MCF-7	breast:
14	chr6:74835506..74837786-chr6:74837930..74840707,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-3	chr6:74779167-74779304	ENSG00000223786.1
2	lnc-CD109-8	chr6:74835887-74836024	ucscGeneNc_uc003phr_2

Variant related genes	Relation type
ENSG00000223786	TF binding region
ENSG00000223786	CpG island

Extended variants
information (count: 1744 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1744 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540726264	chr6:74776839-74776840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72955196	chr6:74776844-74776845	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547384000	chr6:74776854-74776855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566403578	chr6:74776861-74776862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540132234	chr6:74776865-74776866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558108227	chr6:74776892-74776893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367749077	chr6:74776912-74776913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72955199	chr6:74776963-74776964	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189479146	chr6:74776964-74776965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72955201	chr6:74776993-74776994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs12205582	chr6:74777008-74777009	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs541059052	chr6:74777068-74777069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116046152	chr6:74777121-74777122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572057688	chr6:74777136-74777137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545686514	chr6:74777139-74777140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs180753690	chr6:74777151-74777152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544328999	chr6:74777176-74777177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs137995856	chr6:74777194-74777195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199977024	chr6:74777198-74777199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370247417	chr6:74777201-74777202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200774607	chr6:74777205-74777206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201915624	chr6:74777217-74777218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12205749	chr6:74777230-74777231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543224952	chr6:74777254-74777255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149455820	chr6:74777306-74777307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186476747	chr6:74777439-74777440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189398611	chr6:74777443-74777444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114609003	chr6:74777553-74777554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538986238	chr6:74777637-74777638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541889727	chr6:74777671-74777672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532916123	chr6:74777714-74777715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12206043	chr6:74777790-74777791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs79732084	chr6:74777821-74777822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116006972	chr6:74777841-74777842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555664339	chr6:74777846-74777847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567451622	chr6:74777860-74777861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181682630	chr6:74777865-74777866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550172296	chr6:74777929-74777930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552992598	chr6:74777939-74777940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186078378	chr6:74778003-74778004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545029239	chr6:74778030-74778031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558055290	chr6:74778136-74778137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527830398	chr6:74778201-74778202	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369078140	chr6:74778206-74778207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78161550	chr6:74778253-74778254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191340180	chr6:74778279-74778280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183305991	chr6:74778313-74778314	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs561729841	chr6:74778314-74778315	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs117991026	chr6:74778352-74778353	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs367989728	chr6:74778390-74778391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Malignant fibrous histiocytomas	21085701	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74776400-74778600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:74776400-74778800	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:74776400-74783000	Weak transcription	NH-A	brain
4	chr6:74776600-74777000	Enhancers	NHEK	skin
5	chr6:74776600-74777200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:74776600-74778600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:74776600-74778600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:74776600-74778600	Weak transcription	NHDF-Ad	bronchial
9	chr6:74776600-74778600	Weak transcription	Osteobl	bone
10	chr6:74776600-74778800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:74776600-74779200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:74776600-74779400	Weak transcription	HSMM	muscle
13	chr6:74776600-74782800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:74776800-74778800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:74776800-74778800	Weak transcription	HMEC	breast
16	chr6:74776800-74779000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:74777200-74783000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:74778600-74779000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:74778600-74780400	Enhancers	Osteobl	bone
20	chr6:74778600-74780600	Enhancers	NHLF	lung
21	chr6:74778600-74781200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:74778600-74781400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:74778600-74781400	Enhancers	NHDF-Ad	bronchial
24	chr6:74778800-74779000	Enhancers	HMEC	breast
25	chr6:74778800-74779200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:74778800-74779200	Enhancers	Fetal Muscle Leg	muscle
27	chr6:74778800-74780400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:74778800-74783000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:74779000-74779400	Weak transcription	HMEC	breast
30	chr6:74779000-74781600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:74779000-74782800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:74779200-74779400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:74779200-74779800	Active TSS	Fetal Muscle Leg	muscle
34	chr6:74779200-74780400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:74779400-74779600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:74779400-74779600	Enhancers	HSMM	muscle
37	chr6:74779400-74780000	Enhancers	HMEC	breast
38	chr6:74779600-74779800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:74779800-74780000	Flanking Active TSS	Fetal Muscle Leg	muscle
40	chr6:74779800-74781200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:74780000-74780600	Enhancers	Fetal Muscle Leg	muscle
42	chr6:74780000-74782800	Weak transcription	HMEC	breast
43	chr6:74780400-74782800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:74780400-74782800	Weak transcription	Osteobl	bone
45	chr6:74780400-74783200	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr6:74780600-74782800	Weak transcription	Fetal Muscle Leg	muscle
47	chr6:74780600-74782800	Weak transcription	NHLF	lung
48	chr6:74781200-74782800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:74781200-74782800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:74781400-74782800	Weak transcription	NHDF-Ad	bronchial

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