Variant report

Variant	nsv830728
Chromosome Location	chr6:92564379-92785922
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	chr6:92594390-92594453	HepG2	liver:	n/a	n/a
2	BACH1	chr6:92570830-92570878	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:92762476-92762567	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:92710323-92710334	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:92756546-92756984	ECC-1	luminal epithelium:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
6	CEBPB	chr6:92756592-92756837	K562	blood:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
7	CEBPB	chr6:92756582-92756893	A549	lung:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
8	CEBPB	chr6:92599470-92599687	HepG2	liver:	n/a	chr6:92599498-92599509
9	CEBPB	chr6:92672445-92672608	A549	lung:	n/a	chr6:92672572-92672585 chr6:92672558-92672571
10	CEBPB	chr6:92587306-92587436	H1-hESC	embryonic stem cell:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
11	CEBPB	chr6:92735733-92735933	A549	lung:	n/a	chr6:92735909-92735922 chr6:92735909-92735920
12	CEBPB	chr6:92587230-92587530	Hela-S3	cervix:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
13	CEBPB	chr6:92756553-92756907	ECC-1	luminal epithelium:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
14	CEBPB	chr6:92756583-92756895	IMR90	lung:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
15	CEBPB	chr6:92756608-92756937	MCF-7	breast:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
16	CEBPB	chr6:92630170-92630370	HepG2	liver:	n/a	chr6:92630232-92630243
17	CEBPB	chr6:92587233-92587515	IMR90	lung:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
18	CEBPB	chr6:92588057-92588377	HepG2	liver:	n/a	chr6:92588197-92588210 chr6:92588196-92588213 chr6:92588198-92588209
19	CEBPB	chr6:92735798-92736082	HepG2	liver:	n/a	chr6:92735909-92735922 chr6:92735909-92735920
20	CEBPB	chr6:92588068-92588328	A549	lung:	n/a	chr6:92588197-92588210 chr6:92588196-92588213 chr6:92588198-92588209
21	CEBPB	chr6:92587260-92587460	A549	lung:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
22	CEBPB	chr6:92705516-92705572	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:92587252-92587477	HepG2	liver:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
24	CEBPB	chr6:92756606-92756911	HepG2	liver:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
25	CEBPB	chr6:92757585-92757964	ECC-1	luminal epithelium:	n/a	chr6:92757690-92757701
26	CEBPB	chr6:92756609-92756882	H1-hESC	embryonic stem cell:	n/a	chr6:92756750-92756761 chr6:92756749-92756760 chr6:92756751-92756760
27	CEBPB	chr6:92587203-92587495	K562	blood:	n/a	chr6:92587364-92587377 chr6:92587364-92587377 chr6:92587365-92587376
28	CEBPB	chr6:92672380-92672719	Hela-S3	cervix:	n/a	chr6:92672572-92672585 chr6:92672558-92672571
29	CTCF	chr6:92635100-92635250	GM12871	blood:	n/a	n/a
30	CTCF	chr6:92668288-92668414	Medullo	brain:	n/a	n/a
31	CTCF	chr6:92731740-92731834	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:92744340-92744490	Hela-S3	cervix:	n/a	chr6:92744444-92744452 chr6:92744442-92744455
33	CTCF	chr6:92668299-92668397	GM20000	blood:	n/a	n/a
34	CTCF	chr6:92582906-92582983	GM20000	blood:	n/a	n/a
35	CTCF	chr6:92731680-92731830	BE2_C	brain:	n/a	n/a
36	CTCF	chr6:92731660-92731810	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:92613061-92613093	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr6:92744400-92744550	BE2_C	brain:	n/a	chr6:92744444-92744452 chr6:92744442-92744455
39	CTCF	chr6:92586676-92586707	GM20000	blood:	n/a	n/a
40	CTCF	chr6:92731840-92731990	Caco-2	colon:	n/a	n/a
41	CTCF	chr6:92731600-92731750	BE2_C	brain:	n/a	n/a
42	CTCF	chr6:92599543-92599562	GM10248	blood:	n/a	n/a
43	CTCF	chr6:92702399-92702449	GM13976	blood:	n/a	n/a
44	CTCF	chr6:92668319-92668358	GM10266	blood:	n/a	n/a
45	CTCF	chr6:92676492-92676514	GM10266	blood:	n/a	n/a
46	CTCF	chr6:92756040-92756107	Lung_OC	lung:	n/a	n/a
47	CTCF	chr6:92657321-92657379	GM20000	blood:	n/a	n/a
48	E2F4	chr6:92644740-92644868	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr6:92728885-92729133	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr6:92770751-92771060	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:92721775-92721825	H1-hESC	embryonic stem cell:	embryo
2	chr6:92721775-92721825	H1-hESC	embryonic stem cell:	embryo
3	chr6:92721775-92721825	PANC-1	pancreas:	n/a
4	chr6:92636679-92636729	H1-hESC	embryonic stem cell:	embryo
5	chr6:92636767-92636817	HRPEpiC	eye:	n/a
6	chr6:92721775-92721825	PFSK-1	brain:	n/a
7	chr6:92636679-92636729	AG09319	gingival:	n/a
8	chr6:92636301-92636351	HMEC	breast:	n/a
9	chr6:92636306-92636356	U87	brain:	n/a
10	chr6:92636767-92636817	NB4	blood:	n/a
11	chr6:92721775-92721825	PrEC	prostate:	n/a
12	chr6:92636558-92636608	ECC-1	luminal epithelium:	n/a
13	chr6:92636306-92636356	PANC-1	pancreas:	n/a
14	chr6:92636306-92636356	Hela-S3	cervix:	n/a
15	chr6:92721775-92721825	Caco-2	colon:	n/a
16	chr6:92636679-92636729	HEK293	kidney:	embryo
17	chr6:92636306-92636356	HCF	heart:	n/a
18	chr6:92721775-92721825	NHDF-neo	bronchial:	n/a
19	chr6:92636306-92636356	IMR90	lung:	fetal
20	chr6:92636301-92636351	GM12891	blood:	n/a
21	chr6:92636558-92636608	HEK293	kidney:	embryo
22	chr6:92636558-92636608	NT2-D1	testis:	n/a
23	chr6:92636767-92636817	HL-60	blood:	n/a
24	chr6:92636679-92636729	Jurkat	blood:	n/a
25	chr6:92721775-92721825	Hela-S3	cervix:	n/a
26	chr6:92636558-92636608	AG10803	skin:	n/a
27	chr6:92721775-92721825	HRCEpiC	kidney:	n/a
28	chr6:92636767-92636817	PFSK-1	brain:	n/a
29	chr6:92721790-92721840	HCPEpiC	choroid plexus:	n/a
30	chr6:92636301-92636351	AG04450	lung:	fetal
31	chr6:92636306-92636356	HRPEpiC	eye:	n/a
32	chr6:92636767-92636817	CMK	blood:	n/a
33	chr6:92636558-92636608	BJ	skin:	n/a
34	chr6:92636301-92636351	PANC-1	pancreas:	n/a
35	chr6:92636679-92636729	MCF10A-Er-Src	breast:	n/a
36	chr6:92636679-92636729	HRPEpiC	eye:	n/a
37	chr6:92636767-92636817	Hela-S3	cervix:	n/a
38	chr6:92636679-92636729	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:92636679-92636729	BE2_C	brain:	n/a
40	chr6:92721775-92721825	SAEC	small airway:	n/a
41	chr6:92636558-92636608	HCM	heart:	n/a
42	chr6:92636306-92636356	SAEC	small airway:	n/a
43	chr6:92636767-92636817	GM06990	blood:	n/a
44	chr6:92636558-92636608	HUVEC	blood vessel:	n/a
45	chr6:92636306-92636356	HNPCEpiC	eye:	n/a
46	chr6:92636558-92636608	AoSMC	blood vessel:	n/a
47	chr6:92721775-92721825	HCPEpiC	choroid plexus:	n/a
48	chr6:92721790-92721840	HCF	heart:	n/a
49	chr6:92636679-92636729	AG04450	lung:	fetal
50	chr6:92636679-92636729	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:92762402..92765319-chr6:92774985..92777806,2	K562	blood:
2	chr6:92727592..92729242-chr6:92733692..92735310,2	MCF-7	breast:
3	chr6:92727592..92729242-chr6:92733692..92735310,2	MCF-7	breast:
4	chr6:92638341..92640559-chr6:92672574..92674267,2	K562	blood:
5	chr6:92762402..92765319-chr6:92774985..92777806,2	K562	blood:
6	chr6:92638341..92640559-chr6:92672574..92674267,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJA10-22	chr6:92723560-92724452	NONHSAT114001

Variant related genes	Relation type
RPL5P19	TF binding region
RPL5P19	CpG island

Extended variants
information (count: 2270 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2270 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551996184	chr6:92567409-92567410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9451843	chr6:92567443-92567444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs187884388	chr6:92567465-92567466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547364675	chr6:92567487-92567488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567341467	chr6:92567514-92567515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116423623	chr6:92567516-92567517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556389220	chr6:92567627-92567628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376331035	chr6:92567637-92567638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72919169	chr6:92567653-92567654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192778631	chr6:92567657-92567658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557975058	chr6:92567716-92567717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577989016	chr6:92567722-92567723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1391496	chr6:92567800-92567801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184209411	chr6:92567823-92567824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142645912	chr6:92567838-92567839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375891241	chr6:92567863-92567864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572152610	chr6:92567881-92567882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542668468	chr6:92567953-92567954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187918446	chr6:92567988-92567989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531473767	chr6:92568018-92568019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76061736	chr6:92568034-92568035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs5878226	chr6:92568059-92568060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72919170	chr6:92568063-92568064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397725914	chr6:92568068-92568069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116284930	chr6:92568122-92568123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192391009	chr6:92568135-92568136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547697871	chr6:92568223-92568224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567279697	chr6:92568272-92568273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1566219	chr6:92568284-92568285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550197423	chr6:92568318-92568319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184887941	chr6:92568346-92568347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111235751	chr6:92568355-92568356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539159820	chr6:92568368-92568369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189262056	chr6:92568398-92568399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2454243	chr6:92568459-92568460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140429601	chr6:92568464-92568465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554119625	chr6:92568476-92568477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76718622	chr6:92568520-92568521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532308159	chr6:92568526-92568527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192862538	chr6:92568561-92568562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12206127	chr6:92568567-92568568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562537230	chr6:92568589-92568590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576034801	chr6:92568619-92568620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564358479	chr6:92568643-92568644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77420723	chr6:92568644-92568645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550518892	chr6:92568662-92568663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534687395	chr6:92568680-92568681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565100817	chr6:92568779-92568780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189436533	chr6:92568832-92568833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541277960	chr6:92568846-92568847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Endometrioid adenocarcinoma	16974079	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
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	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
Prostate cancer	16573809	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
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	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
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adrenocortical carcinoma	18281524	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Neuropathy	19664229	CNVD
Neurodevelopmental disorder	22521361	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22102821	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:92567400-92567600	Enhancers	Fetal Stomach	stomach
2	chr6:92567600-92569400	Weak transcription	Fetal Stomach	stomach
3	chr6:92569400-92569800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr6:92569400-92569800	Enhancers	Fetal Stomach	stomach
5	chr6:92569800-92570000	Weak transcription	Fetal Stomach	stomach
6	chr6:92570000-92572200	Enhancers	Fetal Stomach	stomach
7	chr6:92570200-92570800	Enhancers	HSMMtube	muscle
8	chr6:92570400-92571000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:92570400-92571000	Enhancers	HMEC	breast
10	chr6:92570600-92571400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:92570800-92571400	Enhancers	Fetal Brain Male	brain
12	chr6:92570800-92571600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:92570800-92572200	Enhancers	Fetal Muscle Leg	muscle
14	chr6:92571000-92574800	Weak transcription	HMEC	breast
15	chr6:92571400-92571800	Enhancers	Left Ventricle	heart
16	chr6:92571400-92575000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:92574800-92576000	Enhancers	HMEC	breast
18	chr6:92575000-92576000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:92575200-92575600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:92575200-92575800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:92575400-92575800	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:92578200-92579200	Enhancers	Liver	Liver
23	chr6:92588000-92589800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:92588800-92589600	Enhancers	Hela-S3	cervix
25	chr6:92589200-92589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:92589200-92589800	Enhancers	HMEC	breast
27	chr6:92594800-92597200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:92605000-92606600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr6:92605200-92605600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:92605200-92606000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:92605200-92606400	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr6:92614400-92615000	Enhancers	Fetal Heart	heart
33	chr6:92636200-92637000	Active TSS	Brain Anterior Caudate	brain
34	chr6:92636600-92637000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:92642000-92642200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:92642800-92643000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:92650200-92650400	Enhancers	Fetal Brain Female	brain
38	chr6:92650400-92651000	Weak transcription	Fetal Brain Female	brain
39	chr6:92650400-92652200	Enhancers	Fetal Brain Male	brain
40	chr6:92651000-92651600	Enhancers	Fetal Brain Female	brain
41	chr6:92670600-92671800	Enhancers	Fetal Brain Male	brain
42	chr6:92671800-92673000	Weak transcription	Fetal Brain Male	brain
43	chr6:92672200-92673200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:92672800-92673200	Enhancers	Adipose Nuclei	Adipose
45	chr6:92672800-92673200	Enhancers	Brain Germinal Matrix	brain
46	chr6:92673000-92673200	Enhancers	Fetal Brain Male	brain
47	chr6:92675200-92676600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr6:92686400-92687000	Enhancers	Hela-S3	cervix
49	chr6:92691800-92692400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:92692000-92692800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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