Variant report

Variant	nsv481691
Chromosome Location	chr6:162663702-163108515
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	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162794306-162794665	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	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
6	ATF1	chr6:162782228-162782581	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	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
11	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
12	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
13	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
14	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
15	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
16	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
17	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
22	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
23	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
24	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
25	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
26	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
27	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
28	CEBPB	chr6:163102596-163102728	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
30	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
32	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
33	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
34	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:163095503-163095821	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
36	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
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	chr6:163036084-163036403	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
39	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
40	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
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	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
43	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
44	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:162672448-162672478	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
48	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
49	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
50	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162683857-162683907	HIPEpiC	eye:	n/a
2	chr6:162864586-162864636	HRPEpiC	eye:	n/a
3	chr6:162683857-162683907	BJ	skin:	n/a
4	chr6:162864586-162864636	GM12892	blood:	n/a
5	chr6:162683881-162683931	NHBE	bronchial:	n/a
6	chr6:162683857-162683907	ProgFib	skin:	n/a
7	chr6:162683961-162684011	NH-A	brain:	n/a
8	chr6:162683857-162683907	GM12878	blood:	n/a
9	chr6:162684441-162684491	AG09309	skin:	n/a
10	chr6:162964378-162964428	CMK	blood:	n/a
11	chr6:162684526-162684576	GM06990	blood:	n/a
12	chr6:162683961-162684011	HCPEpiC	choroid plexus:	n/a
13	chr6:162864586-162864636	GM12878	blood:	n/a
14	chr6:162684526-162684576	Caco-2	colon:	n/a
15	chr6:162964378-162964428	PrEC	prostate:	n/a
16	chr6:162683857-162683907	SK-N-SH	brain:	n/a
17	chr6:162863505-162863555	H1-hESC	embryonic stem cell:	embryo
18	chr6:162964378-162964428	GM19239	blood:	n/a
19	chr6:162684441-162684491	HRPEpiC	eye:	n/a
20	chr6:162683961-162684011	CMK	blood:	n/a
21	chr6:162684441-162684491	MCF10A-Er-Src	breast:	n/a
22	chr6:162964378-162964428	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:162831837-162831887	LNCaP	prostate:	n/a
24	chr6:162684441-162684491	HEEpiC	esophagus:	n/a
25	chr6:162865171-162865221	GM06990	blood:	n/a
26	chr6:162684441-162684491	AoSMC	blood vessel:	n/a
27	chr6:162684526-162684576	AG04450	lung:	fetal
28	chr6:162831837-162831887	AG10803	skin:	n/a
29	chr6:162865171-162865221	HCT-116	colon:	n/a
30	chr6:162865171-162865221	HUVEC	blood vessel:	n/a
31	chr6:162831837-162831887	PrEC	prostate:	n/a
32	chr6:162964378-162964428	NH-A	brain:	n/a
33	chr6:162863505-162863555	HEK293	kidney:	embryo
34	chr6:162683857-162683907	LNCaP	prostate:	n/a
35	chr6:162865171-162865221	SK-N-SH	brain:	n/a
36	chr6:162683881-162683931	AG09309	skin:	n/a
37	chr6:162831837-162831887	SKMC	muscle:	n/a
38	chr6:162865258-162865308	CMK	blood:	n/a
39	chr6:162684441-162684491	PFSK-1	brain:	n/a
40	chr6:163024624-163024674	H1-hESC	embryonic stem cell:	embryo
41	chr6:162831837-162831887	MCF10A-Er-Src	breast:	n/a
42	chr6:162964378-162964428	U87	brain:	n/a
43	chr6:162964378-162964428	ECC-1	luminal epithelium:	n/a
44	chr6:162684526-162684576	NT2-D1	testis:	n/a
45	chr6:162683881-162683931	NT2-D1	testis:	n/a
46	chr6:162864586-162864636	U87	brain:	n/a
47	chr6:162964378-162964428	HRE	kidney:	n/a
48	chr6:162683857-162683907	HRE	kidney:	n/a
49	chr6:163024624-163024674	LNCaP	prostate:	n/a
50	chr6:162864586-162864636	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
2	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
3	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
4	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
5	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
6	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
7	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
8	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
9	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
10	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
11	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
12	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
13	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
14	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
15	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
16	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
17	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
18	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
19	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
20	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
21	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
22	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
23	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
24	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
25	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
26	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
27	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
28	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
29	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: 18168 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:18168 , 50 per page) page: 1 2 3 4 5 6 7 ... 364

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188813292	chr6:162663710-162663711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546548708	chr6:162663743-162663744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553777152	chr6:162663744-162663745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368118367	chr6:162663778-162663779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552390422	chr6:162663780-162663781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569075670	chr6:162663799-162663800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193245118	chr6:162663801-162663802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371583806	chr6:162663807-162663808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554918673	chr6:162663812-162663813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572044021	chr6:162663824-162663825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532544177	chr6:162663834-162663835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542239500	chr6:162663849-162663850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374822913	chr6:162663870-162663871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568057790	chr6:162663927-162663928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533598847	chr6:162663966-162663967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182763875	chr6:162664022-162664023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200695608	chr6:162664039-162664040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368080801	chr6:162664042-162664043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76678030	chr6:162664044-162664045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563609140	chr6:162664053-162664054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187773997	chr6:162664066-162664067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550984653	chr6:162664081-162664082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73783466	chr6:162664109-162664110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542152400	chr6:162664148-162664149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191888952	chr6:162664160-162664161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572304213	chr6:162664175-162664176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117336839	chr6:162664217-162664218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146826895	chr6:162664238-162664239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142554885	chr6:162664253-162664254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11759595	chr6:162664257-162664258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184231603	chr6:162664321-162664322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188566147	chr6:162664323-162664324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146034074	chr6:162664334-162664335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192156126	chr6:162664339-162664340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568686790	chr6:162664347-162664348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534491120	chr6:162664357-162664358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547092467	chr6:162664360-162664361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2023068	chr6:162664364-162664365	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs185109281	chr6:162664375-162664376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556252873	chr6:162664381-162664382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190539752	chr6:162664386-162664387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182377292	chr6:162664429-162664430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200310369	chr6:162664485-162664486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186097937	chr6:162664507-162664508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573331115	chr6:162664516-162664517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541287641	chr6:162664530-162664531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560307541	chr6:162664546-162664547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534383024	chr6:162664562-162664563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576779620	chr6:162664571-162664572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558923400	chr6:162664573-162664574	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
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:1445 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162655200-162688200	Weak transcription	Ovary	ovary
2	chr6:162659000-162666600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:162663600-162664400	Enhancers	Brain Germinal Matrix	brain
4	chr6:162666600-162667000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:162666600-162667200	Enhancers	HepG2	liver
6	chr6:162666800-162667400	Enhancers	Liver	Liver
7	chr6:162667200-162670400	Weak transcription	HepG2	liver
8	chr6:162667400-162670600	Weak transcription	Liver	Liver
9	chr6:162670400-162670800	Enhancers	HepG2	liver
10	chr6:162670600-162670800	Enhancers	Liver	Liver
11	chr6:162670800-162671400	Flanking Active TSS	Liver	Liver
12	chr6:162670800-162671400	Flanking Active TSS	HepG2	liver
13	chr6:162671400-162672400	Enhancers	Liver	Liver
14	chr6:162671400-162672400	Enhancers	HepG2	liver
15	chr6:162674000-162694600	Weak transcription	Aorta	Aorta
16	chr6:162675400-162675800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:162675600-162675800	Enhancers	Brain Anterior Caudate	brain
18	chr6:162675800-162681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:162676600-162676800	Enhancers	Brain Anterior Caudate	brain
20	chr6:162676600-162676800	Enhancers	Left Ventricle	heart
21	chr6:162676800-162677600	Weak transcription	Left Ventricle	heart
22	chr6:162677600-162677800	Enhancers	Left Ventricle	heart
23	chr6:162677600-162677800	Enhancers	Pancreas	Pancrea
24	chr6:162677600-162678000	Enhancers	Fetal Lung	lung
25	chr6:162677800-162679600	Weak transcription	Left Ventricle	heart
26	chr6:162677800-162705400	Weak transcription	Pancreas	Pancrea
27	chr6:162679600-162679800	Enhancers	Left Ventricle	heart
28	chr6:162680800-162682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:162681000-162681400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:162681000-162683800	Weak transcription	Psoas Muscle	Psoas
31	chr6:162681400-162685400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:162682000-162682200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:162682400-162685600	Weak transcription	Brain Anterior Caudate	brain
34	chr6:162682600-162685800	Weak transcription	Fetal Heart	heart
35	chr6:162683000-162683600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:162683200-162684800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:162683600-162684000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:162683600-162684000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:162684000-162684200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:162684000-162685600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:162684200-162685400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:162684800-162685200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:162685200-162685800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr6:162685200-162686000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:162685400-162685600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:162685400-162686000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:162685400-162686000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:162685400-162686000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:162685400-162686200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr6:162685400-162686200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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