Variant report

Variant	nsv1022809
Chromosome Location	chr6:162687401-163001192
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	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
4	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
5	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
6	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
7	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
8	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
9	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
10	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
13	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
14	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
15	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
16	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
17	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
18	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
19	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
20	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
21	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
22	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
23	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
24	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
25	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
26	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
27	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
29	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
30	CEBPB	chr6:162726891-162727117	HepG2	liver:	n/a	chr6:162726998-162727009 chr6:162726998-162727011 chr6:162727074-162727083 chr6:162727018-162727029 chr6:162727072-162727085
31	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
32	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
34	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
35	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
36	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
37	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
38	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
41	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
42	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
43	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
44	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
46	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
47	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
48	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
49	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
50	CEBPD	chr6:162857313-162857505	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162831837-162831887	Hela-S3	cervix:	n/a
2	chr6:162964378-162964428	U87	brain:	n/a
3	chr6:162865171-162865221	LNCaP	prostate:	n/a
4	chr6:162865171-162865221	IMR90	lung:	fetal
5	chr6:162831837-162831887	PrEC	prostate:	n/a
6	chr6:162964378-162964428	HAEpiC	amniotic membrane:	n/a
7	chr6:162831837-162831887	U87	brain:	n/a
8	chr6:162865258-162865308	GM12878	blood:	n/a
9	chr6:162865171-162865221	ovcar-3	ovarian:	n/a
10	chr6:162865171-162865221	Jurkat	blood:	n/a
11	chr6:162865258-162865308	H1-hESC	embryonic stem cell:	embryo
12	chr6:162863505-162863555	AG10803	skin:	n/a
13	chr6:162831837-162831887	AG09309	skin:	n/a
14	chr6:162864586-162864636	AG04449	skin:	fetal
15	chr6:162864586-162864636	NHBE	bronchial:	n/a
16	chr6:162831837-162831887	SAEC	small airway:	n/a
17	chr6:162831837-162831887	ProgFib	skin:	n/a
18	chr6:162831837-162831887	K562	blood:	n/a
19	chr6:162864586-162864636	CMK	blood:	n/a
20	chr6:162863505-162863555	HIPEpiC	eye:	n/a
21	chr6:162865171-162865221	SK-N-SH	brain:	n/a
22	chr6:162865258-162865308	RPTEC	kidney:	n/a
23	chr6:162964378-162964428	AG04449	skin:	fetal
24	chr6:162865258-162865308	HEK293	kidney:	embryo
25	chr6:162863505-162863555	Hela-S3	cervix:	n/a
26	chr6:162964378-162964428	AG04450	lung:	fetal
27	chr6:162863505-162863555	Hepatocyte	liver:	n/a
28	chr6:162964378-162964428	Caco-2	colon:	n/a
29	chr6:162863505-162863555	PrEC	prostate:	n/a
30	chr6:162865258-162865308	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:162863505-162863555	AG04449	skin:	fetal
32	chr6:162864586-162864636	SKMC	muscle:	n/a
33	chr6:162865258-162865308	SKMC	muscle:	n/a
34	chr6:162865171-162865221	HCF	heart:	n/a
35	chr6:162964378-162964428	ProgFib	skin:	n/a
36	chr6:162865258-162865308	AG09309	skin:	n/a
37	chr6:162864586-162864636	HRCEpiC	kidney:	n/a
38	chr6:162863505-162863555	HCPEpiC	choroid plexus:	n/a
39	chr6:162863505-162863555	K562	blood:	n/a
40	chr6:162863505-162863555	SKMC	muscle:	n/a
41	chr6:162865258-162865308	NH-A	brain:	n/a
42	chr6:162864586-162864636	Hela-S3	cervix:	n/a
43	chr6:162864586-162864636	LNCaP	prostate:	n/a
44	chr6:162865171-162865221	A549	lung:	n/a
45	chr6:162863505-162863555	HRPEpiC	eye:	n/a
46	chr6:162831837-162831887	PANC-1	pancreas:	n/a
47	chr6:162964378-162964428	SK-N-SH	brain:	n/a
48	chr6:162831837-162831887	AoSMC	blood vessel:	n/a
49	chr6:162964378-162964428	HIPEpiC	eye:	n/a
50	chr6:162864586-162864636	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
2	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
3	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
4	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
5	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
6	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
7	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
8	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
9	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
10	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
11	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
12	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
13	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
14	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
15	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
16	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
17	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:

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

Extended variants
information (count: 13172 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:13172 , 50 per page) page: 1 2 3 4 5 6 7 ... 264

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35412739	chr6:162687490-162687491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540014183	chr6:162687492-162687493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556938949	chr6:162687498-162687499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550494579	chr6:162687501-162687502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368570901	chr6:162687504-162687505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576636997	chr6:162687506-162687507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535111343	chr6:162687570-162687571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555317771	chr6:162687589-162687590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79711914	chr6:162687612-162687613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540760797	chr6:162687649-162687650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563817530	chr6:162687733-162687734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9355995	chr6:162687778-162687779	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543203515	chr6:162687794-162687795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367562826	chr6:162687796-162687797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529140003	chr6:162687797-162687798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183586433	chr6:162687802-162687803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188718604	chr6:162687809-162687810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6930862	chr6:162687814-162687815	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575142462	chr6:162687831-162687832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6929750	chr6:162687860-162687861	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570952907	chr6:162687865-162687866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181109779	chr6:162687906-162687907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550352649	chr6:162687920-162687921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139714638	chr6:162687969-162687970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536115887	chr6:162687973-162687974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555770186	chr6:162687984-162687985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201317997	chr6:162688026-162688027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572035809	chr6:162688031-162688032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534316113	chr6:162688052-162688053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9458492	chr6:162688112-162688113	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs187109579	chr6:162688114-162688115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552443114	chr6:162688124-162688125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533755085	chr6:162688134-162688135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147483993	chr6:162688176-162688177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191642467	chr6:162688178-162688179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573599730	chr6:162688229-162688230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181694742	chr6:162688247-162688248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368321626	chr6:162688277-162688278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372299706	chr6:162688281-162688282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527729171	chr6:162688290-162688291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541398030	chr6:162688302-162688303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138674526	chr6:162688333-162688334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377474403	chr6:162688335-162688336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372872453	chr6:162688353-162688354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564846364	chr6:162688360-162688361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533440092	chr6:162688369-162688370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187219387	chr6:162688416-162688417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78590835	chr6:162688455-162688456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529443700	chr6:162688486-162688487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549699296	chr6:162688491-162688492	Enhancers 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:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162655200-162688200	Weak transcription	Ovary	ovary
2	chr6:162674000-162694600	Weak transcription	Aorta	Aorta
3	chr6:162677800-162705400	Weak transcription	Pancreas	Pancrea
4	chr6:162687000-162688000	Enhancers	Fetal Heart	heart
5	chr6:162687600-162688800	Enhancers	Fetal Lung	lung
6	chr6:162687800-162688400	Enhancers	Adipose Nuclei	Adipose
7	chr6:162687800-162688600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:162687800-162688600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:162688200-162688400	Enhancers	Ovary	ovary
10	chr6:162688400-162691400	Weak transcription	Adipose Nuclei	Adipose
11	chr6:162688400-162693000	Weak transcription	Ovary	ovary
12	chr6:162692200-162693200	Enhancers	Fetal Muscle Leg	muscle
13	chr6:162697400-162699800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:162698600-162699800	Enhancers	Fetal Heart	heart
15	chr6:162702600-162703000	Weak transcription	Left Ventricle	heart
16	chr6:162702800-162703200	Enhancers	Brain Substantia Nigra	brain
17	chr6:162703000-162703200	Enhancers	Left Ventricle	heart
18	chr6:162705400-162706200	Enhancers	Pancreas	Pancrea
19	chr6:162705600-162706000	Enhancers	HepG2	liver
20	chr6:162705800-162706000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:162708800-162709000	Enhancers	Fetal Muscle Trunk	muscle
22	chr6:162708800-162711400	Enhancers	Fetal Muscle Leg	muscle
23	chr6:162709000-162714400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr6:162709800-162710400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:162710000-162711600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:162710000-162712400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:162710200-162710800	Enhancers	Brain Substantia Nigra	brain
28	chr6:162710400-162719200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr6:162710600-162710800	Enhancers	Brain Cingulate Gyrus	brain
30	chr6:162710600-162711800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:162710600-162712400	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr6:162710800-162711000	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr6:162710800-162711000	Enhancers	Psoas Muscle	Psoas
34	chr6:162710800-162711000	Enhancers	Right Atrium	heart
35	chr6:162710800-162711000	Enhancers	Right Ventricle	heart
36	chr6:162710800-162711200	Active TSS	Brain Anterior Caudate	brain
37	chr6:162710800-162711200	Flanking Active TSS	Brain Cingulate Gyrus	brain
38	chr6:162710800-162711200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr6:162710800-162711400	Enhancers	Brain Angular Gyrus	brain
40	chr6:162710800-162711400	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr6:162710800-162712400	Enhancers	Rectal Smooth Muscle	rectum
42	chr6:162711000-162711200	Active TSS	Brain Hippocampus Middle	brain
43	chr6:162711000-162711200	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr6:162711000-162711400	Enhancers	Fetal Kidney	kidney
45	chr6:162711000-162712200	Weak transcription	Right Atrium	heart
46	chr6:162711000-162712600	Enhancers	Fetal Lung	lung
47	chr6:162711000-162714600	Weak transcription	Right Ventricle	heart
48	chr6:162711200-162711400	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr6:162711200-162711400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr6:162711200-162712200	Weak transcription	Psoas Muscle	Psoas

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