Variant report

Variant	nsv1016439
Chromosome Location	chr6:162676193-163078242
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	chr6:162794306-162794665	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	chr6:163037119-163037243	K562	blood:	n/a	n/a
6	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
7	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
8	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
9	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
10	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
11	ATF3	chr6:162784742-162785052	K562	blood:	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	chr6:162785538-162785848	K562	blood:	n/a	n/a
19	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
20	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
21	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
22	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
23	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
25	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
27	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
28	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
29	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
30	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
31	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
32	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
34	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
35	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
36	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
37	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
38	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
39	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
40	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
41	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
42	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
43	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
44	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
46	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
47	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
48	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
49	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
50	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162683857-162683907	NT2-D1	testis:	n/a
2	chr6:162683857-162683907	NT2-D1	testis:	n/a
3	chr6:162831837-162831887	HCF	heart:	n/a
4	chr6:162865171-162865221	HEEpiC	esophagus:	n/a
5	chr6:162831837-162831887	CMK	blood:	n/a
6	chr6:162864586-162864636	HRCEpiC	kidney:	n/a
7	chr6:162831837-162831887	HRCEpiC	kidney:	n/a
8	chr6:162864586-162864636	A549	lung:	n/a
9	chr6:162683857-162683907	MCF10A-Er-Src	breast:	n/a
10	chr6:162863505-162863555	MCF-7	breast:	n/a
11	chr6:162863505-162863555	T-47D	breast:	n/a
12	chr6:162865171-162865221	Caco-2	colon:	n/a
13	chr6:162831837-162831887	BJ	skin:	n/a
14	chr6:162684526-162684576	BE2_C	brain:	n/a
15	chr6:162964378-162964428	AoSMC	blood vessel:	n/a
16	chr6:162683881-162683931	HCM	heart:	n/a
17	chr6:162683857-162683907	HUVEC	blood vessel:	n/a
18	chr6:162864586-162864636	SK-N-SH	brain:	n/a
19	chr6:162831837-162831887	HAEpiC	amniotic membrane:	n/a
20	chr6:162863505-162863555	HepG2	liver:	n/a
21	chr6:162683881-162683931	PANC-1	pancreas:	n/a
22	chr6:162964378-162964428	NB4	blood:	n/a
23	chr6:162684526-162684576	HCM	heart:	n/a
24	chr6:162864586-162864636	GM12878	blood:	n/a
25	chr6:162683857-162683907	HL-60	blood:	n/a
26	chr6:162683857-162683907	HepG2	liver:	n/a
27	chr6:162864586-162864636	HRPEpiC	eye:	n/a
28	chr6:162865171-162865221	GM12892	blood:	n/a
29	chr6:162683881-162683931	Hepatocyte	liver:	n/a
30	chr6:162865258-162865308	HRCEpiC	kidney:	n/a
31	chr6:162865258-162865308	Jurkat	blood:	n/a
32	chr6:162964378-162964428	SK-N-SH_RA	brain:	n/a
33	chr6:162683881-162683931	Jurkat	blood:	n/a
34	chr6:162864586-162864636	HUVEC	blood vessel:	n/a
35	chr6:162964378-162964428	SKMC	muscle:	n/a
36	chr6:162964378-162964428	BE2_C	brain:	n/a
37	chr6:163024624-163024674	SK-N-SH	brain:	n/a
38	chr6:162683881-162683931	AG09309	skin:	n/a
39	chr6:162865258-162865308	HepG2	liver:	n/a
40	chr6:163024624-163024674	HCM	heart:	n/a
41	chr6:162964378-162964428	A549	lung:	n/a
42	chr6:162683857-162683907	HEK293	kidney:	embryo
43	chr6:162864586-162864636	PrEC	prostate:	n/a
44	chr6:162865171-162865221	AG04450	lung:	fetal
45	chr6:162831837-162831887	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:162964378-162964428	NH-A	brain:	n/a
47	chr6:162865171-162865221	MCF10A-Er-Src	breast:	n/a
48	chr6:162865171-162865221	LNCaP	prostate:	n/a
49	chr6:162864586-162864636	AoSMC	blood vessel:	n/a
50	chr6:162865171-162865221	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
2	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
3	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
4	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
5	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
6	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
7	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
8	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
9	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
10	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
11	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
12	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
13	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
14	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
15	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
16	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
17	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
18	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
19	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
20	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:

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

Extended variants
information (count: 16604 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:16604 , 50 per page) page: 1 2 3 4 5 6 7 ... 333

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6933795	chr6:162676193-162676194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545691371	chr6:162676218-162676219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112973716	chr6:162676264-162676265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559096821	chr6:162676329-162676330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77180051	chr6:162676334-162676335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551425041	chr6:162676340-162676341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563952014	chr6:162676388-162676389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531272814	chr6:162676420-162676421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533198684	chr6:162676490-162676491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529727300	chr6:162676509-162676510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6918198	chr6:162676564-162676565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546636234	chr6:162676565-162676566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140166323	chr6:162676572-162676573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561769093	chr6:162676602-162676603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190006184	chr6:162676605-162676606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143604715	chr6:162676641-162676642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6934605	chr6:162676653-162676654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs76646204	chr6:162676657-162676658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192696221	chr6:162676664-162676665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114257002	chr6:162676711-162676712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184638164	chr6:162676733-162676734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79477113	chr6:162676755-162676756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565500352	chr6:162676758-162676759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556505640	chr6:162676777-162676778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573427117	chr6:162676784-162676785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113315680	chr6:162676789-162676790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542271039	chr6:162676893-162676894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189006553	chr6:162676900-162676901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150022511	chr6:162676928-162676929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181517105	chr6:162676986-162676987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186451460	chr6:162677028-162677029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530797700	chr6:162677042-162677043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190227905	chr6:162677048-162677049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563626036	chr6:162677077-162677078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79557731	chr6:162677079-162677080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6939837	chr6:162677086-162677087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566175355	chr6:162677107-162677108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536044257	chr6:162677115-162677116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535134480	chr6:162677117-162677118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537390259	chr6:162677130-162677131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551936757	chr6:162677161-162677162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571864649	chr6:162677162-162677163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181053826	chr6:162677171-162677172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556544455	chr6:162677258-162677259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372370165	chr6:162677286-162677287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145243645	chr6:162677308-162677309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535839066	chr6:162677314-162677315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552675665	chr6:162677320-162677321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572877758	chr6:162677324-162677325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185954110	chr6:162677325-162677326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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:1359 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

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	chr6:162675800-162681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:162676600-162676800	Enhancers	Brain Anterior Caudate	brain
5	chr6:162676600-162676800	Enhancers	Left Ventricle	heart
6	chr6:162676800-162677600	Weak transcription	Left Ventricle	heart
7	chr6:162677600-162677800	Enhancers	Left Ventricle	heart
8	chr6:162677600-162677800	Enhancers	Pancreas	Pancrea
9	chr6:162677600-162678000	Enhancers	Fetal Lung	lung
10	chr6:162677800-162679600	Weak transcription	Left Ventricle	heart
11	chr6:162677800-162705400	Weak transcription	Pancreas	Pancrea
12	chr6:162679600-162679800	Enhancers	Left Ventricle	heart
13	chr6:162680800-162682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr6:162681000-162681400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:162681000-162683800	Weak transcription	Psoas Muscle	Psoas
16	chr6:162681400-162685400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:162682000-162682200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:162682400-162685600	Weak transcription	Brain Anterior Caudate	brain
19	chr6:162682600-162685800	Weak transcription	Fetal Heart	heart
20	chr6:162683000-162683600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:162683200-162684800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:162683600-162684000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:162683600-162684000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:162684000-162684200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:162684000-162685600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:162684200-162685400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:162684800-162685200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:162685200-162685800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr6:162685200-162686000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:162685400-162685600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:162685400-162686000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr6:162685400-162686000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:162685400-162686000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr6:162685400-162686200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr6:162685400-162686200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:162685400-162686200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:162685600-162685800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:162685600-162686000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:162685600-162686200	Enhancers	Brain Anterior Caudate	brain
40	chr6:162685800-162686000	Enhancers	Fetal Heart	heart
41	chr6:162685800-162686200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:162686000-162687000	Weak transcription	Fetal Heart	heart
43	chr6:162687000-162688000	Enhancers	Fetal Heart	heart
44	chr6:162687600-162688800	Enhancers	Fetal Lung	lung
45	chr6:162687800-162688400	Enhancers	Adipose Nuclei	Adipose
46	chr6:162687800-162688600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:162687800-162688600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr6:162688200-162688400	Enhancers	Ovary	ovary
49	chr6:162688400-162691400	Weak transcription	Adipose Nuclei	Adipose
50	chr6:162688400-162693000	Weak transcription	Ovary	ovary

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