Variant report

Variant	nsv605151
Chromosome Location	chr6:162757114-163044126
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	chr6:162812215-162812339	K562	blood:	n/a	n/a
5	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
6	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
7	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
8	ATF1	chr6:162784797-162785113	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	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:163042376-163042676	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	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
23	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
24	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
25	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
28	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
29	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
30	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
31	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
32	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
33	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
34	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
35	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
36	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
37	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
38	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
39	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
40	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
41	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
42	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
43	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
44	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
45	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
46	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
47	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
48	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
49	CEBPB	chr6:162766353-162766628	IMR90	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
50	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162864586-162864636	AG09319	gingival:	n/a
2	chr6:162865258-162865308	HCM	heart:	n/a
3	chr6:163024624-163024674	GM19239	blood:	n/a
4	chr6:162863505-162863555	HepG2	liver:	n/a
5	chr6:163024624-163024674	Hela-S3	cervix:	n/a
6	chr6:163024624-163024674	HepG2	liver:	n/a
7	chr6:162865171-162865221	T-47D	breast:	n/a
8	chr6:162863505-162863555	HCPEpiC	choroid plexus:	n/a
9	chr6:162864586-162864636	Hepatocyte	liver:	n/a
10	chr6:162865258-162865308	MCF10A-Er-Src	breast:	n/a
11	chr6:162964378-162964428	SK-N-MC	brain:	n/a
12	chr6:162964378-162964428	SAEC	small airway:	n/a
13	chr6:162863505-162863555	HIPEpiC	eye:	n/a
14	chr6:162964378-162964428	AoSMC	blood vessel:	n/a
15	chr6:162864586-162864636	AG09309	skin:	n/a
16	chr6:162864586-162864636	T-47D	breast:	n/a
17	chr6:162865171-162865221	Caco-2	colon:	n/a
18	chr6:162831837-162831887	HL-60	blood:	n/a
19	chr6:162831837-162831887	NH-A	brain:	n/a
20	chr6:162831837-162831887	PANC-1	pancreas:	n/a
21	chr6:162863505-162863555	AG10803	skin:	n/a
22	chr6:162831837-162831887	HRE	kidney:	n/a
23	chr6:162865171-162865221	HCM	heart:	n/a
24	chr6:162864586-162864636	NT2-D1	testis:	n/a
25	chr6:162865258-162865308	HCT-116	colon:	n/a
26	chr6:162865258-162865308	HRCEpiC	kidney:	n/a
27	chr6:162831837-162831887	AG09319	gingival:	n/a
28	chr6:162864586-162864636	HCF	heart:	n/a
29	chr6:162964378-162964428	BE2_C	brain:	n/a
30	chr6:162865258-162865308	HCPEpiC	choroid plexus:	n/a
31	chr6:162863505-162863555	HAEpiC	amniotic membrane:	n/a
32	chr6:162865171-162865221	AG10803	skin:	n/a
33	chr6:162863505-162863555	AoSMC	blood vessel:	n/a
34	chr6:163024624-163024674	HRCEpiC	kidney:	n/a
35	chr6:162865171-162865221	HL-60	blood:	n/a
36	chr6:162864586-162864636	PANC-1	pancreas:	n/a
37	chr6:162865258-162865308	BJ	skin:	n/a
38	chr6:162863505-162863555	Jurkat	blood:	n/a
39	chr6:162964378-162964428	GM12891	blood:	n/a
40	chr6:162964378-162964428	GM06990	blood:	n/a
41	chr6:162831837-162831887	CMK	blood:	n/a
42	chr6:163024624-163024674	BJ	skin:	n/a
43	chr6:162864586-162864636	CMK	blood:	n/a
44	chr6:162864586-162864636	HEEpiC	esophagus:	n/a
45	chr6:162831837-162831887	HAEpiC	amniotic membrane:	n/a
46	chr6:163024624-163024674	HRE	kidney:	n/a
47	chr6:162865171-162865221	GM06990	blood:	n/a
48	chr6:162863505-162863555	HRCEpiC	kidney:	n/a
49	chr6:162964378-162964428	HCM	heart:	n/a
50	chr6:162863505-162863555	HCF	heart:	n/a

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

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

Extended variants
information (count: 12088 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:12088 , 50 per page) page: 1 2 3 4 5 6 7 ... 242

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9346911	chr6:162757114-162757115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142103230	chr6:162757144-162757145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534151097	chr6:162757186-162757187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73026885	chr6:162757208-162757209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556644847	chr6:162757237-162757238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573698380	chr6:162757243-162757244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9365403	chr6:162757251-162757252	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73026886	chr6:162757260-162757261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185249611	chr6:162757270-162757271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575618878	chr6:162757290-162757291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190645575	chr6:162757377-162757378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565185809	chr6:162757431-162757432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181473150	chr6:162757476-162757477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186162327	chr6:162757481-162757482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151313110	chr6:162757497-162757498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74583445	chr6:162757514-162757515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549535517	chr6:162757525-162757526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191903855	chr6:162757528-162757529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35749976	chr6:162757550-162757551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113579364	chr6:162757556-162757557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375757466	chr6:162757567-162757568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559879269	chr6:162757605-162757606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140547602	chr6:162757612-162757613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150485971	chr6:162757624-162757625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571919159	chr6:162757629-162757630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114682167	chr6:162757632-162757633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147733798	chr6:162757644-162757645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567183065	chr6:162757650-162757651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9295186	chr6:162757662-162757663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182849077	chr6:162757667-162757668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187929174	chr6:162757672-162757673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142349412	chr6:162757697-162757698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6911138	chr6:162757723-162757724	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs575515724	chr6:162757740-162757741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544209420	chr6:162757763-162757764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146434130	chr6:162757810-162757811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190797092	chr6:162757865-162757866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574123822	chr6:162757878-162757879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540344408	chr6:162757887-162757888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182319948	chr6:162757907-162757908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73026889	chr6:162757939-162757940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139010524	chr6:162757945-162757946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565310551	chr6:162758028-162758029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117522514	chr6:162758053-162758054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551028717	chr6:162758092-162758093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6911853	chr6:162758106-162758107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187940949	chr6:162758109-162758110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149389036	chr6:162758124-162758125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372159796	chr6:162758126-162758127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143704381	chr6:162758141-162758142	Weak transcription Enhancers	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:1063 , 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	chr6:162753600-162761000	Weak transcription	Adipose Nuclei	Adipose
3	chr6:162755000-162766200	Weak transcription	Ovary	ovary
4	chr6:162757800-162758000	Enhancers	Gastric	stomach
5	chr6:162757800-162758800	Enhancers	Fetal Heart	heart
6	chr6:162758600-162758800	Enhancers	Gastric	stomach
7	chr6:162761400-162761600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:162761600-162766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:162762600-162763000	Weak transcription	Adipose Nuclei	Adipose
10	chr6:162763400-162763800	Enhancers	Fetal Lung	lung
11	chr6:162763600-162764200	Enhancers	Stomach Mucosa	stomach
12	chr6:162763800-162765200	Weak transcription	Fetal Lung	lung
13	chr6:162764000-162764600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:162764400-162764800	Enhancers	Brain Cingulate Gyrus	brain
15	chr6:162764400-162765400	Active TSS	Adipose Nuclei	Adipose
16	chr6:162764400-162766200	Enhancers	Fetal Muscle Leg	muscle
17	chr6:162764400-162766400	Enhancers	NHDF-Ad	bronchial
18	chr6:162764400-162766800	Enhancers	Brain Hippocampus Middle	brain
19	chr6:162764400-162767200	Enhancers	HMEC	breast
20	chr6:162764400-162767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:162764400-162767600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:162764600-162765400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:162764600-162766400	Enhancers	Fetal Brain Male	brain
24	chr6:162764600-162767000	Enhancers	Fetal Heart	heart
25	chr6:162764800-162765400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:162764800-162766200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr6:162765000-162765400	Enhancers	HSMM	muscle
28	chr6:162765000-162765600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr6:162765000-162765800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr6:162765000-162766200	Enhancers	Brain Substantia Nigra	brain
31	chr6:162765000-162766400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:162765000-162766400	Enhancers	Brain Angular Gyrus	brain
33	chr6:162765000-162766400	Enhancers	Right Atrium	heart
34	chr6:162765000-162766800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:162765000-162767200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:162765000-162767200	Enhancers	NHEK	skin
37	chr6:162765200-162765600	Enhancers	Fetal Lung	lung
38	chr6:162765200-162766200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:162765200-162767000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr6:162765400-162765800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:162765400-162765800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr6:162765400-162765800	Enhancers	Adipose Nuclei	Adipose
43	chr6:162765400-162765800	Enhancers	Fetal Brain Female	brain
44	chr6:162765400-162765800	Enhancers	Fetal Muscle Trunk	muscle
45	chr6:162765400-162765800	Weak transcription	HSMM	muscle
46	chr6:162765400-162766600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr6:162765600-162765800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr6:162765600-162765800	Enhancers	Right Ventricle	heart
49	chr6:162765600-162766200	Enhancers	Left Ventricle	heart
50	chr6:162765600-162766200	Enhancers	Pancreas	Pancrea

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