Variant report

Variant	esv3416786
Chromosome Location	chr6:73925761-73958538
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	chr6:73933935-73934276	K562	blood:	n/a	n/a
2	ATF3	chr6:73933914-73934300	K562	blood:	n/a	n/a
3	BHLHE40	chr6:73933933-73934169	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:73933897-73934190	K562	blood:	n/a	n/a
5	CBX3	chr6:73933534-73934385	HCT-116	colon:	n/a	n/a
6	CEBPB	chr6:73935544-73935626	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:73944482-73944921	HCT-116	colon:	n/a	n/a
8	CEBPB	chr6:73942951-73943183	A549	lung:	n/a	chr6:73943037-73943048
9	CEBPB	chr6:73927418-73927765	IMR90	lung:	n/a	chr6:73927593-73927604
10	CEBPB	chr6:73944453-73944896	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:73942971-73943171	HepG2	liver:	n/a	chr6:73943037-73943048
12	CEBPB	chr6:73944448-73944896	A549	lung:	n/a	n/a
13	CEBPB	chr6:73927442-73927728	K562	blood:	n/a	chr6:73927593-73927604
14	CEBPB	chr6:73944525-73944854	A549	lung:	n/a	n/a
15	CEBPB	chr6:73927419-73927762	HepG2	liver:	n/a	chr6:73927593-73927604
16	CEBPB	chr6:73927466-73927741	MCF-7	breast:	n/a	chr6:73927593-73927604
17	CEBPB	chr6:73942958-73943206	Hela-S3	cervix:	n/a	chr6:73943037-73943048
18	CEBPB	chr6:73945840-73946427	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:73944396-73944917	HCT-116	colon:	n/a	n/a
20	CEBPB	chr6:73948065-73948270	A549	lung:	n/a	n/a
21	CEBPB	chr6:73945844-73946543	A549	lung:	n/a	n/a
22	CEBPB	chr6:73942972-73943173	K562	blood:	n/a	chr6:73943037-73943048
23	CEBPB	chr6:73945845-73946426	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:73935502-73935699	MCF-7	breast:	n/a	n/a
25	CEBPB	chr6:73945770-73946272	A549	lung:	n/a	n/a
26	CEBPB	chr6:73927442-73927772	A549	lung:	n/a	chr6:73927593-73927604
27	CEBPB	chr6:73948028-73948327	K562	blood:	n/a	n/a
28	CEBPB	chr6:73944353-73944978	A549	lung:	n/a	n/a
29	CEBPB	chr6:73945771-73946510	A549	lung:	n/a	n/a
30	CEBPB	chr6:73930444-73930619	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:73927447-73927732	H1-hESC	embryonic stem cell:	n/a	chr6:73927593-73927604
32	CEBPB	chr6:73944480-73944880	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:73948005-73948307	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:73938032-73938281	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:73938080-73938262	K562	blood:	n/a	n/a
36	CHD2	chr6:73944551-73944788	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:73935533-73935581	K562	blood:	n/a	n/a
38	CTCF	chr6:73957680-73957830	HepG2	liver:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
39	CTCF	chr6:73935518-73935543	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:73957662-73957734	GM19238	blood:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
41	CTCF	chr6:73935516-73935570	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:73957660-73957810	GM12871	blood:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
43	CTCF	chr6:73957649-73957725	GM12891	blood:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
44	CTCF	chr6:73957642-73957721	H1-hESC	embryonic stem cell:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
45	CTCF	chr6:73951849-73951903	NHEK	skin:	n/a	n/a
46	CTCF	chr6:73957675-73957746	K562	blood:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
47	CTCF	chr6:73957660-73957810	NB4	blood:	n/a	chr6:73957699-73957712 chr6:73957698-73957719 chr6:73957697-73957713 chr6:73957696-73957714 chr6:73957701-73957711 chr6:73957699-73957708
48	CTCF	chr6:73957740-73957890	HAc	cerebellar:	n/a	n/a
49	CTCF	chr6:73935477-73935585	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:73928784-73928825	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:73935125-73935175	HIPEpiC	eye:	n/a
2	chr6:73935676-73935726	AG09309	skin:	n/a
3	chr6:73951939-73951989	SK-N-MC	brain:	n/a
4	chr6:73934576-73934626	RPTEC	kidney:	n/a
5	chr6:73933428-73933478	PANC-1	pancreas:	n/a
6	chr6:73935125-73935175	SK-N-MC	brain:	n/a
7	chr6:73951939-73951989	Hela-S3	cervix:	n/a
8	chr6:73935200-73935250	BE2_C	brain:	n/a
9	chr6:73935584-73935634	RPTEC	kidney:	n/a
10	chr6:73935200-73935250	T-47D	breast:	n/a
11	chr6:73951145-73951195	U87	brain:	n/a
12	chr6:73935584-73935634	Hepatocyte	liver:	n/a
13	chr6:73933428-73933478	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:73935200-73935250	PFSK-1	brain:	n/a
15	chr6:73934576-73934626	SKMC	muscle:	n/a
16	chr6:73935584-73935634	NHBE	bronchial:	n/a
17	chr6:73933428-73933478	PFSK-1	brain:	n/a
18	chr6:73935584-73935634	HL-60	blood:	n/a
19	chr6:73934576-73934626	U87	brain:	n/a
20	chr6:73935125-73935175	SK-N-SH_RA	brain:	n/a
21	chr6:73951145-73951195	BE2_C	brain:	n/a
22	chr6:73935270-73935320	NH-A	brain:	n/a
23	chr6:73935125-73935175	BJ	skin:	n/a
24	chr6:73935676-73935726	ECC-1	luminal epithelium:	n/a
25	chr6:73933428-73933478	GM19239	blood:	n/a
26	chr6:73935270-73935320	HL-60	blood:	n/a
27	chr6:73935200-73935250	HCPEpiC	choroid plexus:	n/a
28	chr6:73951145-73951195	HAEpiC	amniotic membrane:	n/a
29	chr6:73935125-73935175	NHDF-neo	bronchial:	n/a
30	chr6:73934576-73934626	ProgFib	skin:	n/a
31	chr6:73935676-73935726	HRE	kidney:	n/a
32	chr6:73933428-73933478	NHBE	bronchial:	n/a
33	chr6:73935676-73935726	HL-60	blood:	n/a
34	chr6:73935676-73935726	GM12891	blood:	n/a
35	chr6:73935270-73935320	HAEpiC	amniotic membrane:	n/a
36	chr6:73933428-73933478	BE2_C	brain:	n/a
37	chr6:73951145-73951195	GM12878	blood:	n/a
38	chr6:73951939-73951989	HEEpiC	esophagus:	n/a
39	chr6:73935200-73935250	GM06990	blood:	n/a
40	chr6:73935676-73935726	HCM	heart:	n/a
41	chr6:73933428-73933478	AG04449	skin:	fetal
42	chr6:73934576-73934626	A549	lung:	n/a
43	chr6:73935200-73935250	AG04450	lung:	fetal
44	chr6:73935200-73935250	AG04449	skin:	fetal
45	chr6:73951145-73951195	NH-A	brain:	n/a
46	chr6:73935270-73935320	K562	blood:	n/a
47	chr6:73935200-73935250	NHBE	bronchial:	n/a
48	chr6:73934576-73934626	HepG2	liver:	n/a
49	chr6:73951939-73951989	AoSMC	blood vessel:	n/a
50	chr6:73935584-73935634	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:73919854..73922252-chr6:73925613..73927312,3	K562	blood:
2	6:73955774-73958859..6:74099986-74112890	Hela-S3	cervix:
3	6:73946090-73955774..6:74099986-74112890	K562	blood:
4	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:
5	6:73927031-73938730..6:74000304-74012200	K562	blood:
6	6:73859137-73881637..6:73927031-73938730	Hela-S3	cervix:
7	6:73955774-73958859..6:74078047-74099067	Hela-S3	cervix:
8	6:73955774-73958859..6:74062967-74076046	GM12878	blood:
9	6:73955774-73958859..6:74160392-74184826	Hela-S3	cervix:
10	chr6:73917306..73919203-chr6:73947739..73949540,2	K562	blood:
11	6:73927031-73938730..6:73955774-73958859	Hela-S3	cervix:
12	6:73946090-73955774..6:74062967-74076046	GM12878	blood:
13	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:

Variant related genes	Relation type
KHDC1L	TF binding region
KHDC1L	CpG island
ENSG00000235174	chromatin interactions
ENSG00000231332	chromatin interactions
ENSG00000234025	chromatin interactions
ENSG00000256980	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000234882	chromatin interactions
ENSG00000203908	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000207023	chromatin interactions
ENSG00000224221	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000203909	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000164430	chromatin interactions

Extended variants
information (count: 1217 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141584080	chr6:73925799-73925800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186355896	chr6:73925800-73925801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545894881	chr6:73925814-73925815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117633765	chr6:73925822-73925823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374966418	chr6:73925835-73925836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578199745	chr6:73925871-73925872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114812295	chr6:73925877-73925878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35351020	chr6:73925965-73925966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34058074	chr6:73925990-73925991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397886227	chr6:73926002-73926003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543612844	chr6:73926099-73926100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562407779	chr6:73926103-73926104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529515767	chr6:73926119-73926120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536874589	chr6:73926140-73926141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547401575	chr6:73926171-73926172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183190007	chr6:73926172-73926173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186949681	chr6:73926194-73926195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551848154	chr6:73926195-73926196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9446870	chr6:73926196-73926197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs117364459	chr6:73926214-73926215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575411324	chr6:73926243-73926244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549684359	chr6:73926287-73926288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12191533	chr6:73926321-73926322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111824431	chr6:73926344-73926345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553832049	chr6:73926359-73926360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563074525	chr6:73926383-73926384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375890906	chr6:73926385-73926386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60848574	chr6:73926387-73926388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532011234	chr6:73926393-73926394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76234732	chr6:73926431-73926432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60714806	chr6:73926432-73926433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561747258	chr6:73926456-73926457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115529634	chr6:73926480-73926481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9351984	chr6:73926481-73926482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369841954	chr6:73926496-73926497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374584787	chr6:73926497-73926498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562106109	chr6:73926511-73926512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574028122	chr6:73926570-73926571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541302568	chr6:73926571-73926572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559366129	chr6:73926573-73926574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12191673	chr6:73926587-73926588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533145473	chr6:73926605-73926606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73460442	chr6:73926606-73926607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191841028	chr6:73926659-73926660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183034469	chr6:73926726-73926727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs118183299	chr6:73926727-73926728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76841714	chr6:73926805-73926806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77617904	chr6:73926807-73926808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76145975	chr6:73926815-73926816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74789275	chr6:73926816-73926817	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
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:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73916200-73933800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:73928000-73929000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:73931400-73933000	Weak transcription	Ovary	ovary
4	chr6:73931600-73933200	Weak transcription	Fetal Brain Female	brain
5	chr6:73932800-73935200	Weak transcription	Brain Substantia Nigra	brain
6	chr6:73932800-73935200	Weak transcription	Fetal Lung	lung
7	chr6:73933000-73934000	Strong transcription	Ovary	ovary
8	chr6:73933200-73933600	Strong transcription	Fetal Brain Female	brain
9	chr6:73933400-73934200	ZNF genes & repeats	Fetal Stomach	stomach
10	chr6:73933600-73934200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:73933600-73935000	Weak transcription	Fetal Brain Female	brain
12	chr6:73933800-73934000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:73933800-73934000	Enhancers	Spleen	Spleen
14	chr6:73933800-73934200	Flanking Active TSS	K562	blood
15	chr6:73933800-73935200	Enhancers	Placenta	Placenta
16	chr6:73934000-73934200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr6:73934000-73934400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:73934000-73972400	Weak transcription	Ovary	ovary
19	chr6:73934200-73941400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:73934200-73941600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr6:73938000-73938200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:73938200-73938600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:73938400-73941000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:73938600-73943000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:73941000-73941200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:73941000-73941800	Enhancers	Osteobl	bone
27	chr6:73941200-73942200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:73941400-73944000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:73941600-73941800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr6:73941600-73942200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:73941600-73947000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr6:73941800-73942000	Enhancers	NHDF-Ad	bronchial
33	chr6:73941800-73943600	Weak transcription	Osteobl	bone
34	chr6:73942000-73943000	Weak transcription	NHDF-Ad	bronchial
35	chr6:73942200-73945200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:73942600-73942800	Enhancers	NHLF	lung
37	chr6:73942800-73943400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:73943000-73943200	Enhancers	NHDF-Ad	bronchial
39	chr6:73943000-73944000	Weak transcription	NHLF	lung
40	chr6:73943000-73944200	Enhancers	A549	lung
41	chr6:73943000-73944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:73943000-73946600	Enhancers	Hela-S3	cervix
43	chr6:73943000-73946800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:73943200-73943600	Weak transcription	NHDF-Ad	bronchial
45	chr6:73943200-73945200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:73943400-73944400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:73943400-73944600	Enhancers	NHEK	skin
48	chr6:73943600-73944800	Enhancers	Osteobl	bone
49	chr6:73943600-73946800	Enhancers	NHDF-Ad	bronchial
50	chr6:73943800-73944000	Enhancers	Aorta	Aorta

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