Variant report

Variant	esv3475136
Chromosome Location	chr6:73920540-73953198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:551)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 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	ARID3A	chr6:73933935-73934276	K562	blood:	n/a	n/a
2	ATF3	chr6:73933914-73934300	K562	blood:	n/a	n/a
3	BHLHE40	chr6:73933897-73934190	K562	blood:	n/a	n/a
4	BHLHE40	chr6:73933933-73934169	GM12878	blood:	n/a	n/a
5	CBX3	chr6:73933534-73934385	HCT-116	colon:	n/a	n/a
6	CEBPB	chr6:73944482-73944921	HCT-116	colon:	n/a	n/a
7	CEBPB	chr6:73944453-73944896	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr6:73942951-73943183	A549	lung:	n/a	chr6:73943037-73943048
9	CEBPB	chr6:73935544-73935626	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:73935502-73935699	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:73927442-73927728	K562	blood:	n/a	chr6:73927593-73927604
12	CEBPB	chr6:73942971-73943171	HepG2	liver:	n/a	chr6:73943037-73943048
13	CEBPB	chr6:73945771-73946510	A549	lung:	n/a	n/a
14	CEBPB	chr6:73942972-73943173	K562	blood:	n/a	chr6:73943037-73943048
15	CEBPB	chr6:73945770-73946272	A549	lung:	n/a	n/a
16	CEBPB	chr6:73944353-73944978	A549	lung:	n/a	n/a
17	CEBPB	chr6:73945840-73946427	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:73944396-73944917	HCT-116	colon:	n/a	n/a
19	CEBPB	chr6:73938080-73938262	K562	blood:	n/a	n/a
20	CEBPB	chr6:73927447-73927732	H1-hESC	embryonic stem cell:	n/a	chr6:73927593-73927604
21	CEBPB	chr6:73927442-73927772	A549	lung:	n/a	chr6:73927593-73927604
22	CEBPB	chr6:73948028-73948327	K562	blood:	n/a	n/a
23	CEBPB	chr6:73927466-73927741	MCF-7	breast:	n/a	chr6:73927593-73927604
24	CEBPB	chr6:73945845-73946426	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:73945844-73946543	A549	lung:	n/a	n/a
26	CEBPB	chr6:73938032-73938281	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:73927419-73927762	HepG2	liver:	n/a	chr6:73927593-73927604
28	CEBPB	chr6:73944525-73944854	A549	lung:	n/a	n/a
29	CEBPB	chr6:73944480-73944880	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:73942958-73943206	Hela-S3	cervix:	n/a	chr6:73943037-73943048
31	CEBPB	chr6:73927418-73927765	IMR90	lung:	n/a	chr6:73927593-73927604
32	CEBPB	chr6:73948065-73948270	A549	lung:	n/a	n/a
33	CEBPB	chr6:73930444-73930619	IMR90	lung:	n/a	n/a
34	CEBPB	chr6:73948005-73948307	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:73944448-73944896	A549	lung:	n/a	n/a
36	CHD2	chr6:73944551-73944788	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:73928784-73928825	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr6:73935533-73935581	K562	blood:	n/a	n/a
39	CTCF	chr6:73925640-73925790	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:73935477-73935585	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:73925760-73925910	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr6:73937740-73937890	BJ	skin:	n/a	n/a
43	CTCF	chr6:73925760-73925910	HCFaa	heart:	n/a	n/a
44	CTCF	chr6:73927604-73927623	GM13976	blood:	n/a	n/a
45	CTCF	chr6:73951849-73951903	NHEK	skin:	n/a	n/a
46	CTCF	chr6:73935516-73935570	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:73925760-73925910	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr6:73935518-73935543	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:73925740-73925890	AoAF	blood vessel:	n/a	n/a
50	E2F4	chr6:73944567-73944861	MCF10A-Er-Src	breast:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:73933428-73933478	NH-A	brain:	n/a
2	chr6:73951939-73951989	SAEC	small airway:	n/a
3	chr6:73933428-73933478	NH-A	brain:	n/a
4	chr6:73951939-73951989	SAEC	small airway:	n/a
5	chr6:73935676-73935726	HepG2	liver:	n/a
6	chr6:73935200-73935250	A549	lung:	n/a
7	chr6:73935676-73935726	MCF10A-Er-Src	breast:	n/a
8	chr6:73935125-73935175	ovcar-3	ovarian:	n/a
9	chr6:73933428-73933478	NT2-D1	testis:	n/a
10	chr6:73935125-73935175	GM12891	blood:	n/a
11	chr6:73935125-73935175	GM12878	blood:	n/a
12	chr6:73935270-73935320	AG10803	skin:	n/a
13	chr6:73935125-73935175	HCPEpiC	choroid plexus:	n/a
14	chr6:73935676-73935726	HRPEpiC	eye:	n/a
15	chr6:73934576-73934626	HCM	heart:	n/a
16	chr6:73935270-73935320	BE2_C	brain:	n/a
17	chr6:73935676-73935726	HCF	heart:	n/a
18	chr6:73935584-73935634	LNCaP	prostate:	n/a
19	chr6:73935125-73935175	IMR90	lung:	fetal
20	chr6:73935584-73935634	IMR90	lung:	fetal
21	chr6:73935584-73935634	U87	brain:	n/a
22	chr6:73951939-73951989	HRPEpiC	eye:	n/a
23	chr6:73935200-73935250	HEK293	kidney:	embryo
24	chr6:73933428-73933478	PANC-1	pancreas:	n/a
25	chr6:73935584-73935634	SAEC	small airway:	n/a
26	chr6:73935584-73935634	AoSMC	blood vessel:	n/a
27	chr6:73934576-73934626	T-47D	breast:	n/a
28	chr6:73935200-73935250	MCF10A-Er-Src	breast:	n/a
29	chr6:73935200-73935250	HIPEpiC	eye:	n/a
30	chr6:73935200-73935250	NT2-D1	testis:	n/a
31	chr6:73951145-73951195	GM12891	blood:	n/a
32	chr6:73934576-73934626	NT2-D1	testis:	n/a
33	chr6:73935200-73935250	HCPEpiC	choroid plexus:	n/a
34	chr6:73933428-73933478	PrEC	prostate:	n/a
35	chr6:73933428-73933478	BJ	skin:	n/a
36	chr6:73951145-73951195	PrEC	prostate:	n/a
37	chr6:73951145-73951195	AG04450	lung:	fetal
38	chr6:73934576-73934626	IMR90	lung:	fetal
39	chr6:73935270-73935320	SK-N-MC	brain:	n/a
40	chr6:73934576-73934626	HRE	kidney:	n/a
41	chr6:73934576-73934626	Hela-S3	cervix:	n/a
42	chr6:73935125-73935175	AoSMC	blood vessel:	n/a
43	chr6:73935200-73935250	ECC-1	luminal epithelium:	n/a
44	chr6:73935584-73935634	Hepatocyte	liver:	n/a
45	chr6:73935676-73935726	HCM	heart:	n/a
46	chr6:73935200-73935250	AG04450	lung:	fetal
47	chr6:73935200-73935250	HUVEC	blood vessel:	n/a
48	chr6:73951145-73951195	Jurkat	blood:	n/a
49	chr6:73935125-73935175	AG09319	gingival:	n/a
50	chr6:73951145-73951195	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	6:73946090-73955774..6:74062967-74076046	GM12878	blood:
2	6:73859137-73881637..6:73927031-73938730	Hela-S3	cervix:
3	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:
4	6:73927031-73938730..6:74000304-74012200	K562	blood:
5	chr6:73917306..73919203-chr6:73947739..73949540,2	K562	blood:
6	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:
7	chr6:73919854..73922252-chr6:73925613..73927312,3	K562	blood:
8	chr6:73919854..73922252-chr6:73925613..73927312,3	K562	blood:
9	6:73946090-73955774..6:74099986-74112890	K562	blood:

No data

Variant related genes	Relation type
KHDC1L	TF binding region
KHDC1P1	TF binding region
KHDC1L	CpG island
KHDC1P1	CpG island
ENSG00000238464	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000234025	chromatin interactions
ENSG00000203909	chromatin interactions
ENSG00000234882	chromatin interactions
ENSG00000224221	chromatin interactions
ENSG00000203908	chromatin interactions

Extended variants
information (count: 1279 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6453655	chr6:73920553-73920554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559638349	chr6:73920589-73920590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533420620	chr6:73920657-73920658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184727570	chr6:73920724-73920725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11297928	chr6:73920725-73920726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564236561	chr6:73920729-73920730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563330018	chr6:73920733-73920734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369727215	chr6:73920772-73920773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71558908	chr6:73920778-73920779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6935177	chr6:73920780-73920781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6935193	chr6:73920804-73920805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9446868	chr6:73920808-73920809	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566002487	chr6:73920846-73920847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2350372	chr6:73920866-73920867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs76464934	chr6:73920913-73920914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9343019	chr6:73920928-73920929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28718176	chr6:73920995-73920996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2350371	chr6:73920998-73920999	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189101807	chr6:73921013-73921014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555430273	chr6:73921017-73921018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573612313	chr6:73921033-73921034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62411431	chr6:73921055-73921056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185774298	chr6:73921074-73921075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142157788	chr6:73921127-73921128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111544689	chr6:73921181-73921182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35535479	chr6:73921200-73921201	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572337252	chr6:73921229-73921230	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545301808	chr6:73921249-73921250	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572802624	chr6:73921250-73921251	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs530926505	chr6:73921309-73921310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114464596	chr6:73921310-73921311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561438555	chr6:73921343-73921344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544601658	chr6:73921344-73921345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528550389	chr6:73921421-73921422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375475920	chr6:73921429-73921430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191295655	chr6:73921438-73921439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558502701	chr6:73921447-73921448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181237402	chr6:73921451-73921452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540280333	chr6:73921461-73921462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143147596	chr6:73921491-73921492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551697515	chr6:73921520-73921521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116904441	chr6:73921594-73921595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537057897	chr6:73921642-73921643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186110970	chr6:73921654-73921655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148318117	chr6:73921661-73921662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141478246	chr6:73921667-73921668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191010493	chr6:73921686-73921687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577815691	chr6:73921693-73921694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545337011	chr6:73921711-73921712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs57258907	chr6:73921719-73921720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	20409316	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73916200-73933800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:73919400-73920800	Weak transcription	Stomach Mucosa	stomach
3	chr6:73920800-73921000	Enhancers	Stomach Mucosa	stomach
4	chr6:73928000-73929000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:73931400-73933000	Weak transcription	Ovary	ovary
6	chr6:73931600-73933200	Weak transcription	Fetal Brain Female	brain
7	chr6:73932800-73935200	Weak transcription	Brain Substantia Nigra	brain
8	chr6:73932800-73935200	Weak transcription	Fetal Lung	lung
9	chr6:73933000-73934000	Strong transcription	Ovary	ovary
10	chr6:73933200-73933600	Strong transcription	Fetal Brain Female	brain
11	chr6:73933400-73934200	ZNF genes & repeats	Fetal Stomach	stomach
12	chr6:73933600-73934200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:73933600-73935000	Weak transcription	Fetal Brain Female	brain
14	chr6:73933800-73934000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:73933800-73934000	Enhancers	Spleen	Spleen
16	chr6:73933800-73934200	Flanking Active TSS	K562	blood
17	chr6:73933800-73935200	Enhancers	Placenta	Placenta
18	chr6:73934000-73934200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr6:73934000-73934400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:73934000-73972400	Weak transcription	Ovary	ovary
21	chr6:73934200-73941400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:73934200-73941600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr6:73938000-73938200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:73938200-73938600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:73938400-73941000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:73938600-73943000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:73941000-73941200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:73941000-73941800	Enhancers	Osteobl	bone
29	chr6:73941200-73942200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:73941400-73944000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:73941600-73941800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr6:73941600-73942200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:73941600-73947000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr6:73941800-73942000	Enhancers	NHDF-Ad	bronchial
35	chr6:73941800-73943600	Weak transcription	Osteobl	bone
36	chr6:73942000-73943000	Weak transcription	NHDF-Ad	bronchial
37	chr6:73942200-73945200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:73942600-73942800	Enhancers	NHLF	lung
39	chr6:73942800-73943400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:73943000-73943200	Enhancers	NHDF-Ad	bronchial
41	chr6:73943000-73944000	Weak transcription	NHLF	lung
42	chr6:73943000-73944200	Enhancers	A549	lung
43	chr6:73943000-73944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr6:73943000-73946600	Enhancers	Hela-S3	cervix
45	chr6:73943000-73946800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:73943200-73943600	Weak transcription	NHDF-Ad	bronchial
47	chr6:73943200-73945200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:73943400-73944400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:73943400-73944600	Enhancers	NHEK	skin
50	chr6:73943600-73944800	Enhancers	Osteobl	bone

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