Variant report

Variant	nsv538515
Chromosome Location	chr6:162740393-163042505
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	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
4	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
5	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
6	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
7	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
8	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
9	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
10	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
11	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
12	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
13	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
14	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
15	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
19	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
20	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
21	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
22	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
23	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
24	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
25	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
27	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
28	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
29	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
30	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
32	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:162766327-162766640	HepG2	liver:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
35	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
36	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
37	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
38	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
40	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
41	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
42	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
43	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
44	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
45	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
46	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:162766332-162766577	H1-hESC	embryonic stem cell:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
48	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
49	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
50	CEBPB	chr6:162766335-162766614	A549	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162865171-162865221	Hepatocyte	liver:	n/a
2	chr6:162865171-162865221	Hepatocyte	liver:	n/a
3	chr6:162964378-162964428	BJ	skin:	n/a
4	chr6:163024624-163024674	HRPEpiC	eye:	n/a
5	chr6:162831837-162831887	NH-A	brain:	n/a
6	chr6:162865171-162865221	SK-N-SH	brain:	n/a
7	chr6:162864586-162864636	BJ	skin:	n/a
8	chr6:162863505-162863555	Hela-S3	cervix:	n/a
9	chr6:162831837-162831887	CMK	blood:	n/a
10	chr6:162865258-162865308	GM19239	blood:	n/a
11	chr6:162863505-162863555	PANC-1	pancreas:	n/a
12	chr6:162864586-162864636	RPTEC	kidney:	n/a
13	chr6:162865258-162865308	A549	lung:	n/a
14	chr6:162964378-162964428	GM06990	blood:	n/a
15	chr6:162864586-162864636	GM12892	blood:	n/a
16	chr6:162864586-162864636	Caco-2	colon:	n/a
17	chr6:162831837-162831887	ovcar-3	ovarian:	n/a
18	chr6:162863505-162863555	HCPEpiC	choroid plexus:	n/a
19	chr6:162831837-162831887	HIPEpiC	eye:	n/a
20	chr6:163024624-163024674	BE2_C	brain:	n/a
21	chr6:162964378-162964428	HEEpiC	esophagus:	n/a
22	chr6:162865258-162865308	LNCaP	prostate:	n/a
23	chr6:162865171-162865221	HMEC	breast:	n/a
24	chr6:162964378-162964428	MCF-7	breast:	n/a
25	chr6:162865258-162865308	AG04450	lung:	fetal
26	chr6:162865258-162865308	Caco-2	colon:	n/a
27	chr6:162865258-162865308	HEEpiC	esophagus:	n/a
28	chr6:162964378-162964428	HCF	heart:	n/a
29	chr6:162865258-162865308	PrEC	prostate:	n/a
30	chr6:162831837-162831887	HNPCEpiC	eye:	n/a
31	chr6:162831837-162831887	HAEpiC	amniotic membrane:	n/a
32	chr6:162865171-162865221	AoSMC	blood vessel:	n/a
33	chr6:162831837-162831887	Caco-2	colon:	n/a
34	chr6:162865258-162865308	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:162865171-162865221	Jurkat	blood:	n/a
36	chr6:162831837-162831887	GM12892	blood:	n/a
37	chr6:163024624-163024674	HepG2	liver:	n/a
38	chr6:162863505-162863555	NT2-D1	testis:	n/a
39	chr6:162964378-162964428	Caco-2	colon:	n/a
40	chr6:162865171-162865221	SAEC	small airway:	n/a
41	chr6:162865171-162865221	HCF	heart:	n/a
42	chr6:162865258-162865308	AG09319	gingival:	n/a
43	chr6:162864586-162864636	MCF-7	breast:	n/a
44	chr6:162864586-162864636	NB4	blood:	n/a
45	chr6:162964378-162964428	HNPCEpiC	eye:	n/a
46	chr6:163024624-163024674	HCT-116	colon:	n/a
47	chr6:162865258-162865308	HCT-116	colon:	n/a
48	chr6:163024624-163024674	ECC-1	luminal epithelium:	n/a
49	chr6:162964378-162964428	GM12892	blood:	n/a
50	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
4	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
5	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
6	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
7	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
8	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
9	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
10	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
11	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
12	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
13	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
14	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
15	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
16	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
17	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: 12747 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:12747 , 50 per page) page: 1 2 3 4 5 6 7 ... 255

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564873718	chr6:162740426-162740427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572589866	chr6:162740511-162740512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530628556	chr6:162740513-162740514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530426159	chr6:162740516-162740517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs193040010	chr6:162740517-162740518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149082849	chr6:162740522-162740523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117603050	chr6:162740535-162740536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546457966	chr6:162740626-162740627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566735549	chr6:162740643-162740644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534742089	chr6:162740650-162740651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201630997	chr6:162740654-162740655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567270440	chr6:162740659-162740660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146184442	chr6:162740730-162740731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77397400	chr6:162740744-162740745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557605587	chr6:162740793-162740794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370580496	chr6:162740887-162740888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183361239	chr6:162740894-162740895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373085481	chr6:162740902-162740903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536820610	chr6:162740987-162740988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116065002	chr6:162741009-162741010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73598195	chr6:162741037-162741038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544727705	chr6:162741077-162741078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187548906	chr6:162741099-162741100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529122301	chr6:162741153-162741154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191442001	chr6:162741161-162741162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546701507	chr6:162741177-162741178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9365401	chr6:162741184-162741185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183610368	chr6:162741222-162741223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546371808	chr6:162741248-162741249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560227765	chr6:162741253-162741254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532431898	chr6:162741276-162741277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189953679	chr6:162741324-162741325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538833489	chr6:162741345-162741346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571583941	chr6:162741375-162741376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374206551	chr6:162741384-162741385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55793911	chr6:162741395-162741396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370725050	chr6:162741417-162741418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201471337	chr6:162741450-162741451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201106625	chr6:162741452-162741453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542333387	chr6:162741492-162741493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199503719	chr6:162741493-162741494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545329518	chr6:162741502-162741503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537564427	chr6:162741504-162741505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141150002	chr6:162741542-162741543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114989066	chr6:162741550-162741551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550719078	chr6:162741554-162741555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9356001	chr6:162741558-162741559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146922000	chr6:162741570-162741571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9356002	chr6:162741582-162741583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116629515	chr6:162741604-162741605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Schizophrenia	20967226	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162728000-162765600	Weak transcription	Pancreas	Pancrea
2	chr6:162744600-162745000	Active TSS	Primary T killer memory cells from peripheral blood	blood
3	chr6:162745800-162746600	Enhancers	Fetal Brain Male	brain
4	chr6:162746000-162746800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr6:162746200-162746600	Enhancers	Fetal Lung	lung
6	chr6:162746400-162746800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:162746600-162747400	Weak transcription	Fetal Brain Male	brain
8	chr6:162747400-162747600	Enhancers	Fetal Brain Male	brain
9	chr6:162747400-162749800	Weak transcription	Ovary	ovary
10	chr6:162749600-162753000	Weak transcription	Aorta	Aorta
11	chr6:162749800-162750000	Strong transcription	Ovary	ovary
12	chr6:162750000-162753800	Weak transcription	Ovary	ovary
13	chr6:162753200-162753600	Enhancers	Adipose Nuclei	Adipose
14	chr6:162753600-162761000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:162755000-162766200	Weak transcription	Ovary	ovary
16	chr6:162757800-162758000	Enhancers	Gastric	stomach
17	chr6:162757800-162758800	Enhancers	Fetal Heart	heart
18	chr6:162758600-162758800	Enhancers	Gastric	stomach
19	chr6:162761400-162761600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:162761600-162766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:162762600-162763000	Weak transcription	Adipose Nuclei	Adipose
22	chr6:162763400-162763800	Enhancers	Fetal Lung	lung
23	chr6:162763600-162764200	Enhancers	Stomach Mucosa	stomach
24	chr6:162763800-162765200	Weak transcription	Fetal Lung	lung
25	chr6:162764000-162764600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:162764400-162764800	Enhancers	Brain Cingulate Gyrus	brain
27	chr6:162764400-162765400	Active TSS	Adipose Nuclei	Adipose
28	chr6:162764400-162766200	Enhancers	Fetal Muscle Leg	muscle
29	chr6:162764400-162766400	Enhancers	NHDF-Ad	bronchial
30	chr6:162764400-162766800	Enhancers	Brain Hippocampus Middle	brain
31	chr6:162764400-162767200	Enhancers	HMEC	breast
32	chr6:162764400-162767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:162764400-162767600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:162764600-162765400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:162764600-162766400	Enhancers	Fetal Brain Male	brain
36	chr6:162764600-162767000	Enhancers	Fetal Heart	heart
37	chr6:162764800-162765400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr6:162764800-162766200	Weak transcription	Brain Cingulate Gyrus	brain
39	chr6:162765000-162765400	Enhancers	HSMM	muscle
40	chr6:162765000-162765600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr6:162765000-162765800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr6:162765000-162766200	Enhancers	Brain Substantia Nigra	brain
43	chr6:162765000-162766400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:162765000-162766400	Enhancers	Brain Angular Gyrus	brain
45	chr6:162765000-162766400	Enhancers	Right Atrium	heart
46	chr6:162765000-162766800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:162765000-162767200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:162765000-162767200	Enhancers	NHEK	skin
49	chr6:162765200-162765600	Enhancers	Fetal Lung	lung
50	chr6:162765200-162766200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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