Variant report

Variant	nsv605122
Chromosome Location	chr6:162661990-163045463
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	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162671087-162671724	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:162910482-162910786	HepG2	liver:	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	chr6:162782228-162782581	K562	blood:	n/a	n/a
8	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
9	ATF1	chr6:162784797-162785113	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	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
15	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
16	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
18	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
20	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
21	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
22	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
23	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
24	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
25	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
26	CEBPB	chr6:162675613-162675797	A549	lung:	n/a	chr6:162675652-162675661 chr6:162675652-162675661 chr6:162675652-162675663 chr6:162675650-162675661 chr6:162675652-162675661 chr6:162675650-162675663 chr6:162675652-162675661
27	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
28	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
29	CEBPB	chr6:162726891-162727117	HepG2	liver:	n/a	chr6:162726998-162727009 chr6:162726998-162727011 chr6:162727074-162727083 chr6:162727018-162727029 chr6:162727072-162727085
30	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
31	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:162671554-162671904	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
34	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
35	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
36	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
37	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
38	CEBPB	chr6:162670249-162670473	HepG2	liver:	n/a	chr6:162670378-162670389
39	CEBPB	chr6:162671564-162671902	A549	lung:	n/a	n/a
40	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
41	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
42	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
43	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
44	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
46	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
48	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
49	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162964378-162964428	AG04450	lung:	fetal
2	chr6:162964378-162964428	AG04450	lung:	fetal
3	chr6:162683881-162683931	RPTEC	kidney:	n/a
4	chr6:162831837-162831887	SK-N-MC	brain:	n/a
5	chr6:162865171-162865221	HUVEC	blood vessel:	n/a
6	chr6:162864586-162864636	HRE	kidney:	n/a
7	chr6:162683881-162683931	HRPEpiC	eye:	n/a
8	chr6:162683881-162683931	K562	blood:	n/a
9	chr6:162864586-162864636	NHBE	bronchial:	n/a
10	chr6:162683857-162683907	ProgFib	skin:	n/a
11	chr6:162684441-162684491	BJ	skin:	n/a
12	chr6:162683857-162683907	SK-N-MC	brain:	n/a
13	chr6:162831837-162831887	MCF10A-Er-Src	breast:	n/a
14	chr6:163024624-163024674	Hela-S3	cervix:	n/a
15	chr6:163024624-163024674	AG10803	skin:	n/a
16	chr6:162863505-162863555	Hela-S3	cervix:	n/a
17	chr6:162865171-162865221	HRCEpiC	kidney:	n/a
18	chr6:162863505-162863555	PFSK-1	brain:	n/a
19	chr6:162683857-162683907	NB4	blood:	n/a
20	chr6:162683881-162683931	NT2-D1	testis:	n/a
21	chr6:162865171-162865221	GM19239	blood:	n/a
22	chr6:162863505-162863555	GM06990	blood:	n/a
23	chr6:162863505-162863555	A549	lung:	n/a
24	chr6:162683881-162683931	IMR90	lung:	fetal
25	chr6:162964378-162964428	CMK	blood:	n/a
26	chr6:162684441-162684491	LNCaP	prostate:	n/a
27	chr6:162863505-162863555	HCM	heart:	n/a
28	chr6:162865171-162865221	AG09309	skin:	n/a
29	chr6:162683857-162683907	SKMC	muscle:	n/a
30	chr6:162683961-162684011	PFSK-1	brain:	n/a
31	chr6:162683881-162683931	U87	brain:	n/a
32	chr6:162864586-162864636	K562	blood:	n/a
33	chr6:162865258-162865308	BJ	skin:	n/a
34	chr6:163024624-163024674	HMEC	breast:	n/a
35	chr6:162864586-162864636	H1-hESC	embryonic stem cell:	embryo
36	chr6:162864586-162864636	Jurkat	blood:	n/a
37	chr6:162964378-162964428	HCM	heart:	n/a
38	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
39	chr6:162964378-162964428	PANC-1	pancreas:	n/a
40	chr6:162831837-162831887	HEK293	kidney:	embryo
41	chr6:162683857-162683907	ovcar-3	ovarian:	n/a
42	chr6:162864586-162864636	HIPEpiC	eye:	n/a
43	chr6:162683881-162683931	GM12878	blood:	n/a
44	chr6:162864586-162864636	SAEC	small airway:	n/a
45	chr6:162865258-162865308	ECC-1	luminal epithelium:	n/a
46	chr6:162864586-162864636	NB4	blood:	n/a
47	chr6:162863505-162863555	ProgFib	skin:	n/a
48	chr6:162964378-162964428	SK-N-SH_RA	brain:	n/a
49	chr6:162684526-162684576	HMEC	breast:	n/a
50	chr6:162864586-162864636	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
4	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
5	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
6	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
7	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
8	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
9	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
10	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
11	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
12	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
13	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
14	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
15	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
16	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
17	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
18	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
19	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
20	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
21	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
22	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
23	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
24	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: 16223 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:16223 , 50 per page) page: 1 2 3 4 5 6 7 ... 325

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs951196	chr6:162661990-162661991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77171868	chr6:162661999-162662000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139338959	chr6:162662025-162662026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536896854	chr6:162662027-162662028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575793154	chr6:162662044-162662045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553268712	chr6:162662077-162662078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187303261	chr6:162662080-162662081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190435543	chr6:162662102-162662103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564557529	chr6:162662120-162662121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574843959	chr6:162662142-162662143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543914833	chr6:162662143-162662144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560693533	chr6:162662149-162662150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180885232	chr6:162662170-162662171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529751131	chr6:162662192-162662193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80326076	chr6:162662207-162662208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566113220	chr6:162662210-162662211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140450952	chr6:162662231-162662232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186039820	chr6:162662234-162662235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552160796	chr6:162662253-162662254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571677917	chr6:162662254-162662255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4308535	chr6:162662270-162662271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190285572	chr6:162662278-162662279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550990615	chr6:162662281-162662282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567788291	chr6:162662404-162662405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536331242	chr6:162662409-162662410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112929745	chr6:162662448-162662449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573325306	chr6:162662456-162662457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369145516	chr6:162662461-162662462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539320391	chr6:162662514-162662515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558787364	chr6:162662528-162662529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575525202	chr6:162662537-162662538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182480369	chr6:162662544-162662545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560527686	chr6:162662569-162662570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574510202	chr6:162662589-162662590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78704260	chr6:162662618-162662619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs118061842	chr6:162662624-162662625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9347603	chr6:162662674-162662675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560318379	chr6:162662710-162662711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565596052	chr6:162662792-162662793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138228179	chr6:162662827-162662828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562817527	chr6:162662878-162662879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531613583	chr6:162662902-162662903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551027766	chr6:162662956-162662957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565252177	chr6:162662969-162662970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569791529	chr6:162662974-162662975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373431111	chr6:162663033-162663034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185340747	chr6:162663068-162663069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190596341	chr6:162663122-162663123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578156926	chr6:162663132-162663133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182732043	chr6:162663199-162663200	Weak transcription Enhancers	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
Non-syndromic sensorineural hearing loss	21293372	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
Schizophrenia	21346763	CNVD

Chromatin state (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162655200-162688200	Weak transcription	Ovary	ovary
2	chr6:162658600-162663000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:162659000-162666600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:162659200-162663600	Weak transcription	Brain Germinal Matrix	brain
5	chr6:162663000-162663400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:162663600-162664400	Enhancers	Brain Germinal Matrix	brain
7	chr6:162666600-162667000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:162666600-162667200	Enhancers	HepG2	liver
9	chr6:162666800-162667400	Enhancers	Liver	Liver
10	chr6:162667200-162670400	Weak transcription	HepG2	liver
11	chr6:162667400-162670600	Weak transcription	Liver	Liver
12	chr6:162670400-162670800	Enhancers	HepG2	liver
13	chr6:162670600-162670800	Enhancers	Liver	Liver
14	chr6:162670800-162671400	Flanking Active TSS	Liver	Liver
15	chr6:162670800-162671400	Flanking Active TSS	HepG2	liver
16	chr6:162671400-162672400	Enhancers	Liver	Liver
17	chr6:162671400-162672400	Enhancers	HepG2	liver
18	chr6:162674000-162694600	Weak transcription	Aorta	Aorta
19	chr6:162675400-162675800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:162675600-162675800	Enhancers	Brain Anterior Caudate	brain
21	chr6:162675800-162681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:162676600-162676800	Enhancers	Brain Anterior Caudate	brain
23	chr6:162676600-162676800	Enhancers	Left Ventricle	heart
24	chr6:162676800-162677600	Weak transcription	Left Ventricle	heart
25	chr6:162677600-162677800	Enhancers	Left Ventricle	heart
26	chr6:162677600-162677800	Enhancers	Pancreas	Pancrea
27	chr6:162677600-162678000	Enhancers	Fetal Lung	lung
28	chr6:162677800-162679600	Weak transcription	Left Ventricle	heart
29	chr6:162677800-162705400	Weak transcription	Pancreas	Pancrea
30	chr6:162679600-162679800	Enhancers	Left Ventricle	heart
31	chr6:162680800-162682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr6:162681000-162681400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:162681000-162683800	Weak transcription	Psoas Muscle	Psoas
34	chr6:162681400-162685400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:162682000-162682200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:162682400-162685600	Weak transcription	Brain Anterior Caudate	brain
37	chr6:162682600-162685800	Weak transcription	Fetal Heart	heart
38	chr6:162683000-162683600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:162683200-162684800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:162683600-162684000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:162683600-162684000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:162684000-162684200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:162684000-162685600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:162684200-162685400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:162684800-162685200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:162685200-162685800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr6:162685200-162686000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:162685400-162685600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:162685400-162686000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:162685400-162686000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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