Variant report

Variant	nsv966655
Chromosome Location	chr6:117758375-117766294
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	chr6:117762600-117763464	HepG2	liver:	n/a	chr6:117762840-117762856 chr6:117762841-117762857
2	ATF3	chr6:117762158-117762748	A549	lung:	n/a	n/a
3	ATF3	chr6:117762932-117763498	A549	lung:	n/a	n/a
4	ATF3	chr6:117762073-117762812	A549	lung:	n/a	n/a
5	BCL3	chr6:117761816-117762790	A549	lung:	n/a	chr6:117762440-117762449
6	BCL3	chr6:117762828-117763560	A549	lung:	n/a	n/a
7	BCL3	chr6:117762893-117763472	A549	lung:	n/a	n/a
8	BCL3	chr6:117761987-117762782	A549	lung:	n/a	chr6:117762440-117762449
9	BRCA1	chr6:117761605-117762791	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:117765681-117766167	IMR90	lung:	n/a	chr6:117765981-117765992 chr6:117765804-117765817
11	CEBPB	chr6:117762972-117763416	IMR90	lung:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
12	CEBPB	chr6:117761992-117762617	HCT-116	colon:	n/a	chr6:117762474-117762485 chr6:117762474-117762485
13	CEBPB	chr6:117761769-117763564	A549	lung:	n/a	chr6:117762474-117762485 chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117762474-117762485 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117762799-117762810 chr6:117763210-117763221
14	CEBPB	chr6:117763035-117763430	HepG2	liver:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
15	CEBPB	chr6:117763040-117763372	HepG2	liver:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
16	CEBPB	chr6:117761871-117762756	IMR90	lung:	n/a	chr6:117762474-117762485 chr6:117762474-117762485
17	CEBPB	chr6:117762057-117762584	HCT-116	colon:	n/a	chr6:117762474-117762485 chr6:117762474-117762485
18	CEBPB	chr6:117762944-117763517	MCF-7	breast:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
19	CEBPB	chr6:117761806-117762772	A549	lung:	n/a	chr6:117762474-117762485 chr6:117762474-117762485
20	CEBPB	chr6:117762984-117763479	HepG2	liver:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
21	CEBPB	chr6:117762939-117763471	A549	lung:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
22	CEBPB	chr6:117762967-117763495	A549	lung:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
23	CEBPB	chr6:117762954-117763447	MCF-7	breast:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
24	CEBPB	chr6:117761621-117763497	Hela-S3	cervix:	n/a	chr6:117762474-117762485 chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117762474-117762485 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117762799-117762810 chr6:117763210-117763221
25	CEBPB	chr6:117762958-117763446	HepG2	liver:	n/a	chr6:117763106-117763118 chr6:117763228-117763239 chr6:117763159-117763172 chr6:117763228-117763241 chr6:117763230-117763241 chr6:117763159-117763170 chr6:117763230-117763241 chr6:117763210-117763221
26	CEBPB	chr6:117765806-117766124	A549	lung:	n/a	chr6:117765981-117765992
27	CEBPB	chr6:117761850-117762767	A549	lung:	n/a	chr6:117762474-117762485 chr6:117762474-117762485
28	CEBPB	chr6:117765682-117766099	HepG2	liver:	n/a	chr6:117765981-117765992 chr6:117765804-117765817
29	CEBPB	chr6:117765687-117766175	Hela-S3	cervix:	n/a	chr6:117765981-117765992 chr6:117765804-117765817
30	CEBPD	chr6:117763045-117763386	HepG2	liver:	n/a	chr6:117763211-117763222 chr6:117763160-117763171
31	CHD2	chr6:117761787-117762755	Hela-S3	cervix:	n/a	n/a
32	E2F4	chr6:117763732-117763911	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr6:117762012-117762743	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr6:117765440-117766040	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr6:117763825-117763882	GM12878	blood:	n/a	n/a
36	EBF1	chr6:117765161-117765170	GM12878	blood:	n/a	n/a
37	EBF1	chr6:117766001-117766273	GM12878	blood:	n/a	chr6:117766114-117766123 chr6:117766112-117766125 chr6:117766114-117766124 chr6:117766113-117766124
38	ELF1	chr6:117763019-117763356	HepG2	liver:	n/a	n/a
39	ELF1	chr6:117762998-117763323	A549	lung:	n/a	n/a
40	EP300	chr6:117761831-117762785	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr6:117761855-117763033	SK-N-SH	brain:	n/a	n/a
42	EP300	chr6:117765880-117766113	Hela-S3	cervix:	n/a	n/a
43	EP300	chr6:117761753-117763605	A549	lung:	n/a	chr6:117763160-117763174
44	EP300	chr6:117762200-117762717	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr6:117763019-117763416	HepG2	liver:	n/a	chr6:117763160-117763174
46	EP300	chr6:117762967-117763459	HepG2	liver:	n/a	chr6:117763160-117763174
47	EP300	chr6:117761674-117763448	Hela-S3	cervix:	n/a	chr6:117763160-117763174
48	EP300	chr6:117761911-117763010	SK-N-SH	brain:	n/a	n/a
49	EP300	chr6:117761608-117763725	A549	lung:	n/a	chr6:117763160-117763174
50	EP300	chr6:117762890-117763576	HepG2	liver:	n/a	chr6:117763160-117763174

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:117764099..117766879-chr6:117995038..117997863,2	MCF-7	breast:
2	chr6:117763172..117766100-chr6:117768265..117771221,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221434	TF binding region
ENSG00000153989	chromatin interactions

Extended variants
information (count: 348 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140260083	chr6:117758379-117758380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548679904	chr6:117758391-117758392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112525733	chr6:117758426-117758427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373470506	chr6:117758433-117758434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9489178	chr6:117758474-117758475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs537457261	chr6:117758480-117758481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558729340	chr6:117758521-117758522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144827140	chr6:117758525-117758526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386705122	chr6:117758535-117758536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386705123	chr6:117758538-117758539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72957515	chr6:117758539-117758540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189305649	chr6:117758584-117758585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs67157504	chr6:117758643-117758644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs72432097	chr6:117758647-117758648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150345199	chr6:117758656-117758657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72957517	chr6:117758665-117758666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs72957518	chr6:117758681-117758682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs545771692	chr6:117758694-117758695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184323134	chr6:117758697-117758698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376771596	chr6:117758703-117758704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564104872	chr6:117758707-117758708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189561686	chr6:117758726-117758727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369699529	chr6:117758727-117758728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs72957520	chr6:117758739-117758740	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555846862	chr6:117758749-117758750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548346864	chr6:117758753-117758754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537244765	chr6:117758788-117758789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530948977	chr6:117758793-117758794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79424407	chr6:117758796-117758797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79393268	chr6:117758800-117758801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4266519	chr6:117758802-117758803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552530370	chr6:117758811-117758812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181212335	chr6:117758848-117758849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186412023	chr6:117758854-117758855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145937128	chr6:117758862-117758863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4266520	chr6:117758874-117758875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567864785	chr6:117758875-117758876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557225167	chr6:117758904-117758905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563187160	chr6:117758926-117758927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75563571	chr6:117758927-117758928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76950554	chr6:117758928-117758929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535633055	chr6:117758952-117758953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115587991	chr6:117758953-117758954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28839542	chr6:117759078-117759079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575280666	chr6:117759102-117759103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191205514	chr6:117759122-117759123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9489181	chr6:117759128-117759129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs572891365	chr6:117759149-117759150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138232670	chr6:117759165-117759166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9489182	chr6:117759172-117759173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:115)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	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
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Epilepsy	22083797	CNVD
Cancer	17440070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117747600-117760600	Weak transcription	Osteobl	bone
2	chr6:117753200-117760200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr6:117753800-117760000	Weak transcription	HSMM	muscle
4	chr6:117753800-117760400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:117757800-117760400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:117758600-117758800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:117758800-117760200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:117760000-117761200	ZNF genes & repeats	HSMM	muscle
9	chr6:117760000-117762000	Enhancers	Hela-S3	cervix
10	chr6:117760000-117762600	Enhancers	HMEC	breast
11	chr6:117760200-117760400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr6:117760200-117761000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:117760400-117760800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:117760400-117761400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
15	chr6:117760600-117761200	ZNF genes & repeats	Osteobl	bone
16	chr6:117760600-117761400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:117760800-117761000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:117760800-117761200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:117760800-117761400	ZNF genes & repeats	NHEK	skin
20	chr6:117761000-117761200	ZNF genes & repeats	A549	lung
21	chr6:117761000-117762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:117761000-117762600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:117761200-117762000	Weak transcription	Osteobl	bone
24	chr6:117761200-117762200	Weak transcription	A549	lung
25	chr6:117761200-117762800	Weak transcription	HSMM	muscle
26	chr6:117761200-117763400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:117761400-117761600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:117761400-117761600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr6:117761400-117761600	Weak transcription	NHEK	skin
30	chr6:117761600-117762800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:117761600-117762800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr6:117761600-117763800	Enhancers	NHEK	skin
33	chr6:117761800-117762200	Enhancers	Placenta	Placenta
34	chr6:117761800-117763400	Enhancers	NHDF-Ad	bronchial
35	chr6:117761800-117763600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:117762000-117762200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:117762000-117762400	Weak transcription	Hela-S3	cervix
38	chr6:117762000-117762800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:117762000-117763400	Enhancers	NH-A	brain
40	chr6:117762000-117763400	Enhancers	NHLF	lung
41	chr6:117762000-117763800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:117762000-117764600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:117762000-117767800	Enhancers	Osteobl	bone
44	chr6:117762200-117762400	Enhancers	A549	lung
45	chr6:117762200-117762600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:117762200-117763400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:117762200-117763400	Enhancers	HSMMtube	muscle
48	chr6:117762400-117762600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:117762400-117762600	Weak transcription	A549	lung
50	chr6:117762400-117764400	Enhancers	Hela-S3	cervix

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