Variant report

Variant	nsv886161
Chromosome Location	chr6:74765488-74800529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:74775980-74776424	IMR90	lung:	n/a	n/a
2	CEBPB	chr6:74785098-74785334	H1-hESC	embryonic stem cell:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
3	CEBPB	chr6:74779883-74780137	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:74795063-74795245	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:74785083-74785369	IMR90	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
6	CEBPB	chr6:74785096-74785355	HepG2	liver:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
7	CEBPB	chr6:74786135-74786343	A549	lung:	n/a	chr6:74786167-74786179 chr6:74786208-74786219 chr6:74786206-74786219 chr6:74786206-74786217
8	CEBPB	chr6:74766470-74766684	HepG2	liver:	n/a	chr6:74766585-74766596
9	CEBPB	chr6:74790615-74790619	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:74786155-74786301	HepG2	liver:	n/a	chr6:74786167-74786179 chr6:74786208-74786219 chr6:74786206-74786219 chr6:74786206-74786217
11	CEBPB	chr6:74766515-74766703	H1-hESC	embryonic stem cell:	n/a	chr6:74766585-74766596
12	CEBPB	chr6:74785013-74785395	HCT-116	colon:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
13	CEBPB	chr6:74785109-74785309	A549	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
14	CEBPB	chr6:74784948-74785495	HCT-116	colon:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
15	CEBPB	chr6:74785099-74785398	Hela-S3	cervix:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
16	CEBPB	chr6:74783207-74783464	IMR90	lung:	n/a	n/a
17	CHD1	chr6:74797580-74798127	IMR90	lung:	n/a	n/a
18	CTCF	chr6:74797720-74797870	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr6:74783800-74783950	AG10803	skin:	n/a	n/a
20	CTCF	chr6:74776260-74776410	SAEC	small airway:	n/a	n/a
21	CTCF	chr6:74797740-74797890	HMF	breast:	n/a	n/a
22	CTCF	chr6:74797820-74797970	NHLF	lung:	n/a	n/a
23	CTCF	chr6:74797733-74797869	LNCaP	prostate:	n/a	n/a
24	CTCF	chr6:74797640-74797790	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr6:74797760-74797910	HRE	kidney:	n/a	n/a
26	CTCF	chr6:74797640-74797790	RPTEC	kidney:	n/a	n/a
27	CTCF	chr6:74798548-74798551	GM10266	blood:	n/a	n/a
28	CTCF	chr6:74797740-74797890	AG09319	gingival:	n/a	n/a
29	CTCF	chr6:74785240-74785390	AG10803	skin:	n/a	n/a
30	CTCF	chr6:74797590-74798133	HCT-116	colon:	n/a	n/a
31	CTCF	chr6:74797740-74797890	HVMF	connective:	n/a	n/a
32	CTCF	chr6:74800340-74800490	HVMF	connective:	n/a	n/a
33	CTCF	chr6:74783780-74783930	AG09309	skin:	n/a	n/a
34	CTCF	chr6:74797680-74797830	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr6:74798559-74798578	GM10266	blood:	n/a	n/a
36	CTCF	chr6:74797763-74797823	ProgFib	skin:	n/a	n/a
37	CTCF	chr6:74785140-74785290	HMEC	breast:	n/a	n/a
38	CTCF	chr6:74797740-74797890	HPF	lung:	n/a	n/a
39	CTCF	chr6:74797720-74797870	AG04450	lung:	n/a	n/a
40	CTCF	chr6:74797760-74797910	HMEC	breast:	n/a	n/a
41	CTCF	chr6:74797720-74797870	BJ	skin:	n/a	n/a
42	CTCF	chr6:74783760-74783910	AG09319	gingival:	n/a	n/a
43	CTCF	chr6:74797700-74797850	AG04449	skin:	n/a	n/a
44	CTCF	chr6:74797720-74797870	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr6:74797760-74797910	AG09309	skin:	n/a	n/a
46	CTCF	chr6:74783796-74783913	Fibrobl	skin:	n/a	n/a
47	CTCF	chr6:74797780-74797930	HCM	heart:	n/a	n/a
48	CTCF	chr6:74797740-74797890	HCM	heart:	n/a	n/a
49	CTCF	chr6:74797665-74797901	GM12878	blood:	n/a	n/a
50	CTCF	chr6:74797740-74797890	AG04449	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	chr6:74778313-74778363	BE2_C	brain:	n/a
2	chr6:74784340-74784390	HEK293	kidney:	embryo
3	chr6:74778313-74778363	HCF	heart:	n/a
4	chr6:74778313-74778363	PANC-1	pancreas:	n/a
5	chr6:74778945-74778995	SAEC	small airway:	n/a
6	chr6:74784340-74784390	NB4	blood:	n/a
7	chr6:74784340-74784390	HEEpiC	esophagus:	n/a
8	chr6:74778945-74778995	Hepatocyte	liver:	n/a
9	chr6:74778945-74778995	NT2-D1	testis:	n/a
10	chr6:74784340-74784390	HCF	heart:	n/a
11	chr6:74778313-74778363	AG04449	skin:	fetal
12	chr6:74778313-74778363	AG09319	gingival:	n/a
13	chr6:74778313-74778363	SK-N-MC	brain:	n/a
14	chr6:74778313-74778363	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:74778313-74778363	HEK293	kidney:	embryo
16	chr6:74784340-74784390	Hela-S3	cervix:	n/a
17	chr6:74778945-74778995	NHBE	bronchial:	n/a
18	chr6:74778313-74778363	T-47D	breast:	n/a
19	chr6:74784340-74784390	SK-N-SH	brain:	n/a
20	chr6:74778945-74778995	Jurkat	blood:	n/a
21	chr6:74778945-74778995	T-47D	breast:	n/a
22	chr6:74778945-74778995	SK-N-SH	brain:	n/a
23	chr6:74784340-74784390	PrEC	prostate:	n/a
24	chr6:74784340-74784390	SK-N-MC	brain:	n/a
25	chr6:74778945-74778995	Caco-2	colon:	n/a
26	chr6:74778945-74778995	HL-60	blood:	n/a
27	chr6:74778313-74778363	ProgFib	skin:	n/a
28	chr6:74778945-74778995	HMEC	breast:	n/a
29	chr6:74778945-74778995	BJ	skin:	n/a
30	chr6:74778313-74778363	PFSK-1	brain:	n/a
31	chr6:74778945-74778995	AG09319	gingival:	n/a
32	chr6:74778945-74778995	AoSMC	blood vessel:	n/a
33	chr6:74784340-74784390	A549	lung:	n/a
34	chr6:74778313-74778363	PrEC	prostate:	n/a
35	chr6:74778313-74778363	LNCaP	prostate:	n/a
36	chr6:74784340-74784390	AG09319	gingival:	n/a
37	chr6:74784340-74784390	ProgFib	skin:	n/a
38	chr6:74778945-74778995	ovcar-3	ovarian:	n/a
39	chr6:74778945-74778995	GM06990	blood:	n/a
40	chr6:74778313-74778363	A549	lung:	n/a
41	chr6:74778945-74778995	GM12878	blood:	n/a
42	chr6:74778945-74778995	CMK	blood:	n/a
43	chr6:74778945-74778995	IMR90	lung:	fetal
44	chr6:74778945-74778995	HAEpiC	amniotic membrane:	n/a
45	chr6:74784340-74784390	GM06990	blood:	n/a
46	chr6:74784340-74784390	MCF-7	breast:	n/a
47	chr6:74778313-74778363	GM12892	blood:	n/a
48	chr6:74784340-74784390	HCM	heart:	n/a
49	chr6:74778313-74778363	Jurkat	blood:	n/a
50	chr6:74778945-74778995	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74564800..74565363-chr6:74797356..74797902,2	MCF-7	breast:
2	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-3	chr6:74779167-74779304	ENSG00000223786.1

No data

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

Extended variants
information (count: 737 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377458197	chr6:74769827-74769828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7745566	chr6:74769852-74769853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191477434	chr6:74769895-74769896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs80062875	chr6:74769920-74769921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59147259	chr6:74769946-74769947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111802759	chr6:74769947-74769948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541103480	chr6:74769950-74769951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559680027	chr6:74769985-74769986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs57583486	chr6:74770060-74770061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527624115	chr6:74770075-74770076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117047336	chr6:74770088-74770089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572478926	chr6:74770097-74770098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563157456	chr6:74770108-74770109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184396115	chr6:74770125-74770126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531408145	chr6:74770168-74770169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs56396434	chr6:74770191-74770192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568079310	chr6:74770200-74770201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188885589	chr6:74770433-74770434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539399146	chr6:74770453-74770454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75731530	chr6:74770459-74770460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117607760	chr6:74770480-74770481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537655735	chr6:74770497-74770498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114561891	chr6:74770498-74770499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564599673	chr6:74770514-74770515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75362493	chr6:74770529-74770530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574076226	chr6:74770584-74770585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193250136	chr6:74770685-74770686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532070877	chr6:74770713-74770714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117362131	chr6:74770739-74770740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577626822	chr6:74770746-74770747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370613840	chr6:74770821-74770822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544957353	chr6:74770851-74770852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564063624	chr6:74770856-74770857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13200840	chr6:74770939-74770940	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs138960134	chr6:74770965-74770966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561899276	chr6:74771021-74771022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13200871	chr6:74771075-74771076	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185324107	chr6:74771100-74771101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549809345	chr6:74771125-74771126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74965651	chr6:74771127-74771128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539460967	chr6:74771174-74771175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557293288	chr6:74771204-74771205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149399495	chr6:74771216-74771217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371503025	chr6:74771225-74771226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555727379	chr6:74771236-74771237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574171668	chr6:74771261-74771262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528446374	chr6:74771381-74771382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534869051	chr6:74771386-74771387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6937604	chr6:74771389-74771390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577690001	chr6:74771433-74771434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	22522925	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74769800-74770200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr6:74770400-74771000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:74771000-74775800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:74775000-74776600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:74775400-74776200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:74775400-74776400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:74775400-74776400	Enhancers	Fetal Muscle Leg	muscle
8	chr6:74775400-74776600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:74775600-74776000	Enhancers	HMEC	breast
10	chr6:74775600-74776600	Enhancers	Osteobl	bone
11	chr6:74775800-74776000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:74775800-74776000	Enhancers	NHEK	skin
13	chr6:74775800-74776600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:74775800-74776600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:74775800-74776600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr6:74775800-74776600	Enhancers	NHDF-Ad	bronchial
17	chr6:74775800-74776800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:74776000-74776400	Flanking Active TSS	HMEC	breast
19	chr6:74776000-74776600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:74776000-74776600	Flanking Active TSS	NHEK	skin
21	chr6:74776200-74776400	Enhancers	NH-A	brain
22	chr6:74776200-74776600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:74776200-74776600	Enhancers	HSMM	muscle
24	chr6:74776400-74776600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:74776400-74776800	Enhancers	HMEC	breast
26	chr6:74776400-74778600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:74776400-74778800	Weak transcription	Fetal Muscle Leg	muscle
28	chr6:74776400-74783000	Weak transcription	NH-A	brain
29	chr6:74776600-74777000	Enhancers	NHEK	skin
30	chr6:74776600-74777200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:74776600-74778600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:74776600-74778600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:74776600-74778600	Weak transcription	NHDF-Ad	bronchial
34	chr6:74776600-74778600	Weak transcription	Osteobl	bone
35	chr6:74776600-74778800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr6:74776600-74779200	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr6:74776600-74779400	Weak transcription	HSMM	muscle
38	chr6:74776600-74782800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:74776800-74778800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:74776800-74778800	Weak transcription	HMEC	breast
41	chr6:74776800-74779000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:74777200-74783000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:74778600-74779000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:74778600-74780400	Enhancers	Osteobl	bone
45	chr6:74778600-74780600	Enhancers	NHLF	lung
46	chr6:74778600-74781200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:74778600-74781400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:74778600-74781400	Enhancers	NHDF-Ad	bronchial
49	chr6:74778800-74779000	Enhancers	HMEC	breast
50	chr6:74778800-74779200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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