Variant report

Variant	nsv1020023
Chromosome Location	chr6:162617012-163070805
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	chr6:162671087-162671724	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
5	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
6	ATF1	chr6:162784797-162785113	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	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
10	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
11	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
12	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
13	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
14	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
15	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
16	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
18	BRCA1	chr6:162658617-162658742	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
21	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
22	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
23	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
24	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
25	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
26	CEBPB	chr6:162672448-162672478	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
28	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
29	CEBPB	chr6:162656289-162656489	A549	lung:	n/a	n/a
30	CEBPB	chr6:162634276-162634544	A549	lung:	n/a	chr6:162634418-162634429
31	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:162675529-162675821	HepG2	liver:	n/a	chr6:162675652-162675661 chr6:162675652-162675661 chr6:162675652-162675663 chr6:162675650-162675661 chr6:162675652-162675661 chr6:162675650-162675663 chr6:162675652-162675661
33	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
34	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
35	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
36	CEBPB	chr6:162670249-162670473	HepG2	liver:	n/a	chr6:162670378-162670389
37	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
38	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
39	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
40	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
41	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
42	CEBPB	chr6:162726891-162727117	HepG2	liver:	n/a	chr6:162726998-162727009 chr6:162726998-162727011 chr6:162727074-162727083 chr6:162727018-162727029 chr6:162727072-162727085
43	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
44	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
45	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:162656180-162656471	HepG2	liver:	n/a	chr6:162656287-162656298 chr6:162656286-162656299
47	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
48	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162683857-162683907	AG04450	lung:	fetal
2	chr6:162964378-162964428	U87	brain:	n/a
3	chr6:162683857-162683907	AG04450	lung:	fetal
4	chr6:162964378-162964428	U87	brain:	n/a
5	chr6:162964378-162964428	AG10803	skin:	n/a
6	chr6:162683857-162683907	PrEC	prostate:	n/a
7	chr6:162864586-162864636	ProgFib	skin:	n/a
8	chr6:162865258-162865308	K562	blood:	n/a
9	chr6:162864586-162864636	HUVEC	blood vessel:	n/a
10	chr6:162683881-162683931	GM19239	blood:	n/a
11	chr6:162864586-162864636	HCT-116	colon:	n/a
12	chr6:162683961-162684011	H1-hESC	embryonic stem cell:	embryo
13	chr6:163024624-163024674	HCF	heart:	n/a
14	chr6:162683881-162683931	LNCaP	prostate:	n/a
15	chr6:162683961-162684011	LNCaP	prostate:	n/a
16	chr6:162865171-162865221	NB4	blood:	n/a
17	chr6:162683881-162683931	IMR90	lung:	fetal
18	chr6:162684526-162684576	HCM	heart:	n/a
19	chr6:162831837-162831887	PANC-1	pancreas:	n/a
20	chr6:162684526-162684576	SK-N-MC	brain:	n/a
21	chr6:162684441-162684491	SK-N-SH	brain:	n/a
22	chr6:163024624-163024674	HAEpiC	amniotic membrane:	n/a
23	chr6:162684526-162684576	HepG2	liver:	n/a
24	chr6:162864586-162864636	HRCEpiC	kidney:	n/a
25	chr6:162684526-162684576	Hela-S3	cervix:	n/a
26	chr6:163024624-163024674	Jurkat	blood:	n/a
27	chr6:162865258-162865308	GM12891	blood:	n/a
28	chr6:162831837-162831887	GM19239	blood:	n/a
29	chr6:162864586-162864636	Jurkat	blood:	n/a
30	chr6:162863505-162863555	HIPEpiC	eye:	n/a
31	chr6:163024624-163024674	HRE	kidney:	n/a
32	chr6:162831837-162831887	GM12878	blood:	n/a
33	chr6:163024624-163024674	NT2-D1	testis:	n/a
34	chr6:162683881-162683931	NHBE	bronchial:	n/a
35	chr6:162684526-162684576	HIPEpiC	eye:	n/a
36	chr6:162683961-162684011	K562	blood:	n/a
37	chr6:162683857-162683907	HRCEpiC	kidney:	n/a
38	chr6:163024624-163024674	GM06990	blood:	n/a
39	chr6:162863505-162863555	SAEC	small airway:	n/a
40	chr6:162865171-162865221	HL-60	blood:	n/a
41	chr6:162865258-162865308	HCM	heart:	n/a
42	chr6:162684441-162684491	HNPCEpiC	eye:	n/a
43	chr6:163024624-163024674	HEK293	kidney:	embryo
44	chr6:162683961-162684011	MCF-7	breast:	n/a
45	chr6:163024624-163024674	K562	blood:	n/a
46	chr6:162683881-162683931	AG09309	skin:	n/a
47	chr6:162863505-162863555	GM06990	blood:	n/a
48	chr6:163024624-163024674	GM12878	blood:	n/a
49	chr6:162863505-162863555	HRE	kidney:	n/a
50	chr6:162683857-162683907	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
2	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
3	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
4	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
5	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
6	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
7	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
8	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
9	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:
10	chr6:162613600..162615384-chr6:162617227..162618872,2	K562	blood:
11	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
12	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
13	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
14	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
15	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
16	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
17	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:
18	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
19	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
20	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
21	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
22	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
23	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
24	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
25	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
26	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
27	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
28	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
29	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:

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

Extended variants
information (count: 19160 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:19160 , 50 per page) page: 1 2 3 4 5 6 7 ... 384

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1954943	chr6:162617012-162617013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560818829	chr6:162617018-162617019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34691811	chr6:162617058-162617059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529709358	chr6:162617089-162617090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78357013	chr6:162617120-162617121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117034716	chr6:162617132-162617133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566427647	chr6:162617183-162617184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532361002	chr6:162617195-162617196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569075121	chr6:162617231-162617232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367900846	chr6:162617248-162617249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552056549	chr6:162617310-162617311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144217959	chr6:162617344-162617345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537709944	chr6:162617354-162617355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191947823	chr6:162617427-162617428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183323909	chr6:162617448-162617449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552997490	chr6:162617449-162617450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140830903	chr6:162617499-162617500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553468034	chr6:162617550-162617551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144754041	chr6:162617559-162617560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545605908	chr6:162617569-162617570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147896984	chr6:162617570-162617571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9456751	chr6:162617643-162617644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs200465933	chr6:162617650-162617651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114813904	chr6:162617655-162617656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142216048	chr6:162617660-162617661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6929127	chr6:162617676-162617677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs540687981	chr6:162617735-162617736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189072414	chr6:162617783-162617784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559095136	chr6:162617801-162617802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532071757	chr6:162617806-162617807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76829436	chr6:162617846-162617847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552360855	chr6:162617856-162617857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545708805	chr6:162617889-162617890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193022052	chr6:162617895-162617896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182453140	chr6:162617934-162617935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548121880	chr6:162617949-162617950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375920187	chr6:162617950-162617951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186784166	chr6:162617952-162617953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142161343	chr6:162617967-162617968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386708037	chr6:162618008-162618009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7741375	chr6:162618009-162618010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538711770	chr6:162618019-162618020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544492671	chr6:162618055-162618056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559005264	chr6:162618121-162618122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372934927	chr6:162618135-162618136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573190416	chr6:162618176-162618177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575949183	chr6:162618247-162618248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376423863	chr6:162618252-162618253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151224181	chr6:162618263-162618264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184105717	chr6:162618265-162618266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Parkinson disease	21829596	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	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	17122850	CNVD

Chromatin state (count:1511 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162605800-162624200	Weak transcription	Pancreas	Pancrea
2	chr6:162609600-162622000	Weak transcription	Left Ventricle	heart
3	chr6:162609600-162622400	Weak transcription	Psoas Muscle	Psoas
4	chr6:162613000-162621600	Weak transcription	Spleen	Spleen
5	chr6:162613000-162622000	Weak transcription	Right Atrium	heart
6	chr6:162615800-162617200	Enhancers	Fetal Heart	heart
7	chr6:162616200-162617200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:162617200-162621800	Weak transcription	Fetal Heart	heart
9	chr6:162618800-162619200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:162619000-162619400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:162619000-162619400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr6:162619200-162622000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr6:162619800-162620000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr6:162620600-162620800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:162620800-162621400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:162620800-162623000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:162620800-162623000	Enhancers	Adipose Nuclei	Adipose
18	chr6:162621000-162622800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr6:162621200-162622200	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr6:162621600-162622000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:162621600-162622400	Enhancers	Fetal Stomach	stomach
22	chr6:162621800-162622200	Enhancers	Fetal Kidney	kidney
23	chr6:162621800-162623000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:162621800-162623000	Enhancers	Fetal Heart	heart
25	chr6:162622000-162622200	Enhancers	Right Ventricle	heart
26	chr6:162622000-162622400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr6:162622000-162622400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:162622000-162622400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr6:162622000-162622400	Enhancers	Fetal Brain Male	brain
30	chr6:162622000-162622400	Enhancers	Left Ventricle	heart
31	chr6:162622000-162622400	Enhancers	Rectal Smooth Muscle	rectum
32	chr6:162622000-162622400	Enhancers	Right Atrium	heart
33	chr6:162622000-162622400	Active TSS	Stomach Smooth Muscle	stomach
34	chr6:162622000-162622600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:162622000-162623000	Enhancers	Colon Smooth Muscle	Colon
36	chr6:162622200-162622800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr6:162622400-162622600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:162622400-162622800	Enhancers	Psoas Muscle	Psoas
39	chr6:162622400-162624200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr6:162622400-162624400	Weak transcription	Aorta	Aorta
41	chr6:162622400-162624400	Weak transcription	Fetal Stomach	stomach
42	chr6:162622400-162632000	Weak transcription	Left Ventricle	heart
43	chr6:162622400-162636000	Weak transcription	Right Atrium	heart
44	chr6:162622600-162623000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:162622800-162623000	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr6:162622800-162624200	Weak transcription	Psoas Muscle	Psoas
47	chr6:162622800-162624200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr6:162623000-162623200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:162623000-162624000	Weak transcription	Fetal Heart	heart
50	chr6:162623000-162624200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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