Variant report

Variant	nsv481708
Chromosome Location	chr6:162842569-163051741
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	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
3	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
4	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
5	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
6	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
7	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
8	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
9	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
13	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
14	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
15	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
16	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
17	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
18	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
19	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
20	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
21	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
22	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
25	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
26	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
28	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
29	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
32	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
34	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
35	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
36	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
37	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
39	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
40	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
41	CEBPD	chr6:162857313-162857505	HepG2	liver:	n/a	n/a
42	CHD2	chr6:162863812-162864012	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:162874863-162874897	GM13977	blood:	n/a	n/a
44	CTCF	chr6:162863800-162863950	HA-sp	spinal cord:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932
45	CTCF	chr6:162863500-162863650	GM12865	blood:	n/a	n/a
46	CTCF	chr6:162977821-162977975	MCF-7	breast:	n/a	chr6:162977884-162977902
47	CTCF	chr6:163033767-163033941	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:162863820-162863970	HBMEC	blood vessel:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932
49	CTCF	chr6:163041298-163041411	GM12878	blood:	n/a	chr6:163041356-163041369 chr6:163041349-163041370 chr6:163041354-163041372
50	CTCF	chr6:162863820-162863970	GM12871	blood:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162865258-162865308	ProgFib	skin:	n/a
2	chr6:162865258-162865308	ProgFib	skin:	n/a
3	chr6:163024624-163024674	BJ	skin:	n/a
4	chr6:162865171-162865221	HRCEpiC	kidney:	n/a
5	chr6:162964378-162964428	HRE	kidney:	n/a
6	chr6:162864586-162864636	GM12891	blood:	n/a
7	chr6:162865258-162865308	AG09319	gingival:	n/a
8	chr6:162865171-162865221	HNPCEpiC	eye:	n/a
9	chr6:162864586-162864636	U87	brain:	n/a
10	chr6:162863505-162863555	SK-N-SH	brain:	n/a
11	chr6:162865171-162865221	GM12891	blood:	n/a
12	chr6:162865258-162865308	AoSMC	blood vessel:	n/a
13	chr6:163024624-163024674	NB4	blood:	n/a
14	chr6:162863505-162863555	HRPEpiC	eye:	n/a
15	chr6:162964378-162964428	ECC-1	luminal epithelium:	n/a
16	chr6:162865258-162865308	ovcar-3	ovarian:	n/a
17	chr6:162964378-162964428	AG09319	gingival:	n/a
18	chr6:162964378-162964428	IMR90	lung:	fetal
19	chr6:163024624-163024674	PFSK-1	brain:	n/a
20	chr6:162864586-162864636	NHDF-neo	bronchial:	n/a
21	chr6:162865171-162865221	HCF	heart:	n/a
22	chr6:162864586-162864636	ECC-1	luminal epithelium:	n/a
23	chr6:162864586-162864636	PANC-1	pancreas:	n/a
24	chr6:162863505-162863555	A549	lung:	n/a
25	chr6:162863505-162863555	MCF10A-Er-Src	breast:	n/a
26	chr6:162864586-162864636	HEK293	kidney:	embryo
27	chr6:162864586-162864636	AG04450	lung:	fetal
28	chr6:162865258-162865308	Hela-S3	cervix:	n/a
29	chr6:162863505-162863555	AG10803	skin:	n/a
30	chr6:162865258-162865308	AG04450	lung:	fetal
31	chr6:162864586-162864636	HCM	heart:	n/a
32	chr6:163024624-163024674	HCT-116	colon:	n/a
33	chr6:162865171-162865221	PFSK-1	brain:	n/a
34	chr6:162864586-162864636	SAEC	small airway:	n/a
35	chr6:162964378-162964428	NH-A	brain:	n/a
36	chr6:162964378-162964428	GM12891	blood:	n/a
37	chr6:163024624-163024674	Hela-S3	cervix:	n/a
38	chr6:162964378-162964428	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:162865258-162865308	HEK293	kidney:	embryo
40	chr6:162865171-162865221	HL-60	blood:	n/a
41	chr6:162865171-162865221	NT2-D1	testis:	n/a
42	chr6:162865258-162865308	HAEpiC	amniotic membrane:	n/a
43	chr6:162863505-162863555	ECC-1	luminal epithelium:	n/a
44	chr6:162865258-162865308	HCT-116	colon:	n/a
45	chr6:162864586-162864636	SK-N-MC	brain:	n/a
46	chr6:162865258-162865308	NH-A	brain:	n/a
47	chr6:162863505-162863555	HRE	kidney:	n/a
48	chr6:162964378-162964428	HUVEC	blood vessel:	n/a
49	chr6:162964378-162964428	PrEC	prostate:	n/a
50	chr6:162865258-162865308	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
2	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
3	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
4	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
5	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
6	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
7	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
8	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 8966 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:8966 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184146616	chr6:162842600-162842601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527528731	chr6:162842605-162842606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541204701	chr6:162842636-162842637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377250893	chr6:162842657-162842658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7746087	chr6:162842722-162842723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533089002	chr6:162842725-162842726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550019244	chr6:162842739-162842740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7766912	chr6:162842740-162842741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7746196	chr6:162842762-162842763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs116717834	chr6:162842896-162842897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13216887	chr6:162842921-162842922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149321321	chr6:162842922-162842923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79940882	chr6:162842951-162842952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570676748	chr6:162842999-162843000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9364655	chr6:162843020-162843021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112448017	chr6:162843037-162843038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188448362	chr6:162843074-162843075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144465583	chr6:162843170-162843171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530303900	chr6:162843276-162843277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555157900	chr6:162843281-162843282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10455908	chr6:162843312-162843313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs35602343	chr6:162843317-162843318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555528392	chr6:162843354-162843355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181641639	chr6:162843441-162843442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541092110	chr6:162843464-162843465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116761013	chr6:162843538-162843539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533098842	chr6:162843566-162843567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543364178	chr6:162843567-162843568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541083947	chr6:162843572-162843573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6911087	chr6:162843596-162843597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184387848	chr6:162843609-162843610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190129907	chr6:162843616-162843617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548158916	chr6:162843657-162843658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561881495	chr6:162843682-162843683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35246470	chr6:162843724-162843725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs6937749	chr6:162843725-162843726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570715289	chr6:162843747-162843748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540013605	chr6:162843748-162843749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550253638	chr6:162843752-162843753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9347635	chr6:162843757-162843758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570306915	chr6:162843775-162843776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200915990	chr6:162843794-162843795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140432232	chr6:162843810-162843811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575880530	chr6:162843829-162843830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142465172	chr6:162843839-162843840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371529931	chr6:162843889-162843890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534708871	chr6:162843903-162843904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557848868	chr6:162843917-162843918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577803053	chr6:162843935-162843936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543604064	chr6:162843942-162843943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162838000-162863600	Weak transcription	Aorta	Aorta
2	chr6:162838600-162868800	Weak transcription	Left Ventricle	heart
3	chr6:162839000-162860800	Weak transcription	Ovary	ovary
4	chr6:162841000-162842600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:162844000-162859600	Weak transcription	Psoas Muscle	Psoas
6	chr6:162851800-162852400	Enhancers	Fetal Heart	heart
7	chr6:162856800-162857200	Enhancers	Liver	Liver
8	chr6:162856800-162857600	Enhancers	HepG2	liver
9	chr6:162859000-162860400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:162859200-162860200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:162859400-162864800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:162859600-162860400	ZNF genes & repeats	Psoas Muscle	Psoas
13	chr6:162859600-162863600	Weak transcription	Brain Angular Gyrus	brain
14	chr6:162860000-162860200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr6:162860000-162861000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:162860000-162861200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:162860000-162861200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr6:162860000-162861200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:162860200-162860400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:162860200-162860600	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr6:162860200-162861400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:162860400-162860600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr6:162860400-162861800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:162860400-162862200	Weak transcription	Psoas Muscle	Psoas
25	chr6:162860600-162860800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr6:162860600-162861200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr6:162860600-162862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr6:162860800-162861200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:162860800-162864000	Strong transcription	Ovary	ovary
30	chr6:162860800-162864600	Weak transcription	Adipose Nuclei	Adipose
31	chr6:162861000-162863400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:162861200-162862600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr6:162861200-162862600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:162861200-162863200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr6:162861400-162865800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:162861800-162863200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:162861800-162872600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr6:162862200-162864200	Weak transcription	Right Ventricle	heart
39	chr6:162862600-162864200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:162862600-162864200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:162862600-162864600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:162863000-162864000	Enhancers	Brain Germinal Matrix	brain
43	chr6:162863000-162864200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr6:162863000-162864600	Enhancers	Fetal Brain Female	brain
45	chr6:162863000-162865000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr6:162863200-162863400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:162863200-162863400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:162863200-162863600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:162863200-162863800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr6:162863200-162865200	Enhancers	Cortex derived primary cultured neurospheres	brain

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