Variant report

Variant	nsv525815
Chromosome Location	chr6:165017873-165262895
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:366)
Chromatin interactive
region (count:22)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:165055640-165055827	K562	blood:	n/a	n/a
2	CEBPB	chr6:165241508-165241767	HepG2	liver:	n/a	n/a
3	CEBPB	chr6:165081130-165081446	HepG2	liver:	n/a	chr6:165081280-165081291
4	CEBPB	chr6:165102542-165102851	HepG2	liver:	n/a	chr6:165102690-165102703 chr6:165102692-165102701 chr6:165102690-165102701 chr6:165102692-165102701 chr6:165102690-165102703 chr6:165102692-165102701
5	CEBPB	chr6:165162502-165162828	HepG2	liver:	n/a	chr6:165162656-165162667
6	CEBPB	chr6:165162515-165162798	IMR90	lung:	n/a	chr6:165162656-165162667
7	CEBPB	chr6:165054168-165054395	HepG2	liver:	n/a	chr6:165054256-165054267
8	CEBPB	chr6:165224170-165224453	IMR90	lung:	n/a	chr6:165224322-165224333
9	CEBPB	chr6:165114994-165115342	H1-hESC	embryonic stem cell:	n/a	chr6:165115254-165115265 chr6:165115153-165115166
10	CEBPB	chr6:165224152-165224514	HepG2	liver:	n/a	chr6:165224322-165224333
11	CTCF	chr6:165033758-165034133	GM12878	blood:	n/a	n/a
12	CTCF	chr6:165033860-165034010	GM12878	blood:	n/a	n/a
13	CTCF	chr6:165111260-165111410	GM12868	blood:	n/a	n/a
14	CTCF	chr6:165033840-165033990	GM06990	blood:	n/a	n/a
15	CTCF	chr6:165165527-165165549	GM20000	blood:	n/a	n/a
16	CTCF	chr6:165172620-165172770	K562	blood:	n/a	n/a
17	CTCF	chr6:165131623-165131724	Fibrobl	skin:	n/a	n/a
18	CTCF	chr6:165252392-165252423	LNCaP	prostate:	n/a	n/a
19	CTCF	chr6:165033820-165033970	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr6:165023128-165023198	ProgFib	skin:	n/a	n/a
21	CTCF	chr6:165032013-165032133	GM12892	blood:	n/a	chr6:165032057-165032070 chr6:165032049-165032059
22	CTCF	chr6:165033840-165033990	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:165243120-165243270	GM12864	blood:	n/a	n/a
24	CTCF	chr6:165032037-165032096	ProgFib	skin:	n/a	chr6:165032057-165032070 chr6:165032049-165032059
25	CTCF	chr6:165073473-165073521	GM13977	blood:	n/a	n/a
26	CTCF	chr6:165176146-165176199	GM10266	blood:	n/a	n/a
27	CTCF	chr6:165238960-165239110	GM12865	blood:	n/a	n/a
28	CTCF	chr6:165033888-165034014	GM12878	blood:	n/a	n/a
29	CTCF	chr6:165033900-165034050	RPTEC	kidney:	n/a	n/a
30	CTCF	chr6:165033910-165034012	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr6:165033885-165034016	LNCaP	prostate:	n/a	n/a
32	CTCF	chr6:165237960-165238110	NHLF	lung:	n/a	n/a
33	CTCF	chr6:165165300-165165450	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr6:165150132-165150215	GM13976	blood:	n/a	n/a
35	CTCF	chr6:165033877-165034044	LNCaP	prostate:	n/a	n/a
36	E2F4	chr6:165241064-165241372	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr6:165240349-165240549	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr6:165033777-165034074	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr6:165033779-165034070	GM12878	blood:	n/a	n/a
40	E2F4	chr6:165082126-165082515	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr6:165051814-165052081	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr6:165042350-165042550	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr6:165063936-165063938	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr6:165033939-165033964	GM12878	blood:	n/a	n/a
45	EP300	chr6:165250014-165250362	MCF-7	breast:	n/a	n/a
46	EP300	chr6:165200785-165201082	GM12878	blood:	n/a	n/a
47	EP300	chr6:165209197-165209257	GM12878	blood:	n/a	n/a
48	EP300	chr6:165254506-165254533	K562	blood:	n/a	n/a
49	EP300	chr6:165152593-165152826	SK-N-SH_RA	brain:	n/a	chr6:165152734-165152748
50	EP300	chr6:165086348-165086801	MCF-7	breast:	n/a	chr6:165086631-165086644 chr6:165086564-165086573

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165032068-165032118	HIPEpiC	eye:	n/a
2	chr6:165032124-165032174	NB4	blood:	n/a
3	chr6:165115084-165115134	NHBE	bronchial:	n/a
4	chr6:165236522-165236572	GM12891	blood:	n/a
5	chr6:165236522-165236572	Caco-2	colon:	n/a
6	chr6:165115084-165115134	GM12878	blood:	n/a
7	chr6:165032068-165032118	CMK	blood:	n/a
8	chr6:165236522-165236572	ECC-1	luminal epithelium:	n/a
9	chr6:165032072-165032122	ECC-1	luminal epithelium:	n/a
10	chr6:165032072-165032122	Caco-2	colon:	n/a
11	chr6:165236522-165236572	HCM	heart:	n/a
12	chr6:165032124-165032174	HL-60	blood:	n/a
13	chr6:165062070-165062120	HRPEpiC	eye:	n/a
14	chr6:165236522-165236572	NHBE	bronchial:	n/a
15	chr6:165032068-165032118	AG09319	gingival:	n/a
16	chr6:165115084-165115134	PrEC	prostate:	n/a
17	chr6:165032124-165032174	AG09309	skin:	n/a
18	chr6:165236522-165236572	BJ	skin:	n/a
19	chr6:165032068-165032118	HRCEpiC	kidney:	n/a
20	chr6:165062070-165062120	AG10803	skin:	n/a
21	chr6:165062070-165062120	ovcar-3	ovarian:	n/a
22	chr6:165032068-165032118	HCPEpiC	choroid plexus:	n/a
23	chr6:165032072-165032122	HIPEpiC	eye:	n/a
24	chr6:165236522-165236572	NT2-D1	testis:	n/a
25	chr6:165115084-165115134	HNPCEpiC	eye:	n/a
26	chr6:165032072-165032122	A549	lung:	n/a
27	chr6:165115084-165115134	AG04450	lung:	fetal
28	chr6:165032068-165032118	AoSMC	blood vessel:	n/a
29	chr6:165032072-165032122	PrEC	prostate:	n/a
30	chr6:165115084-165115134	HL-60	blood:	n/a
31	chr6:165115084-165115134	IMR90	lung:	fetal
32	chr6:165032072-165032122	GM12891	blood:	n/a
33	chr6:165032124-165032174	BJ	skin:	n/a
34	chr6:165032068-165032118	Jurkat	blood:	n/a
35	chr6:165032072-165032122	HepG2	liver:	n/a
36	chr6:165115084-165115134	HRE	kidney:	n/a
37	chr6:165032068-165032118	HL-60	blood:	n/a
38	chr6:165032124-165032174	BE2_C	brain:	n/a
39	chr6:165062070-165062120	GM19239	blood:	n/a
40	chr6:165115084-165115134	AoSMC	blood vessel:	n/a
41	chr6:165062070-165062120	GM06990	blood:	n/a
42	chr6:165236522-165236572	GM12878	blood:	n/a
43	chr6:165032124-165032174	K562	blood:	n/a
44	chr6:165032124-165032174	SKMC	muscle:	n/a
45	chr6:165236522-165236572	HEEpiC	esophagus:	n/a
46	chr6:165236522-165236572	SKMC	muscle:	n/a
47	chr6:165032124-165032174	SK-N-SH	brain:	n/a
48	chr6:165236522-165236572	PrEC	prostate:	n/a
49	chr6:165236522-165236572	HMEC	breast:	n/a
50	chr6:165032068-165032118	NB4	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:128797111..128797864-chr6:165136910..165137454,2	MCF-7	breast:
2	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
3	chr6:165085847..165087840-chr6:165089357..165091527,2	K562	blood:
4	chr6:165249458..165251438-chr6:165253089..165255770,2	K562	blood:
5	chr6:165110029..165112755-chr6:165114733..165117071,2	K562	blood:
6	chr6:165160068..165160918-chr8:98129240..98129986,2	MCF-7	breast:
7	chr6:165117997..165120289-chr6:165120644..165122440,2	K562	blood:
8	chr6:165259094..165261615-chr6:165279301..165280809,2	K562	blood:
9	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
10	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
11	chr6:165082238..165084641-chr6:165089609..165091881,2	K562	blood:
12	chr6:165249458..165251438-chr6:165253089..165255770,2	K562	blood:
13	chr6:165085847..165087840-chr6:165089357..165091527,2	K562	blood:
14	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
15	chr6:165244240..165245853-chr6:165247412..165249558,2	K562	blood:
16	chr6:165117997..165120289-chr6:165120644..165122440,2	K562	blood:
17	chr6:165082238..165084641-chr6:165089609..165091881,2	K562	blood:
18	chr6:165110029..165112755-chr6:165114733..165117071,2	K562	blood:
19	chr6:165007452..165009387-chr6:165042540..165044932,2	K562	blood:
20	chr6:164768274..164768906-chr6:165033273..165034147,2	MCF-7	breast:
21	chr6:165244240..165245853-chr6:165247412..165249558,2	K562	blood:
22	chr6:165119728..165120228-chrX:107366674..107367661,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-1	chr6:165219185-165219218	XLOC_005915
2	lnc-C6orf118-1	chr6:165219185-165219218	NONHSAT115991
3	lnc-C6orf118-1	chr6:165218447-165218582	XLOC_005915
4	lnc-QKI-12	chr6:165163000-165163096	NONHSAT115989
5	lnc-C6orf118-5	chr6:165138435-165138569	ucscGeneNc_uc003qul_1
6	lnc-C6orf118-5	chr6:165155417-165155532	ucscGeneNc_uc003qul_1
7	lnc-C6orf118-1	chr6:165207066-165207641	NONHSAT115991
8	lnc-QKI-4	chr6:165244510-165244543	NONHSAT115996
9	lnc-QKI-4	chr6:165243010-165243106	XLOC_005533
10	lnc-C6orf118-5	chr6:165139175-165139208	ucscGeneNc_uc003qul_1
11	lnc-QKI-4	chr6:165241238-165241452	NONHSAT115993
12	lnc-QKI-4	chr6:165241239-165245119	ENSG00000227455.2
13	lnc-QKI-12	chr6:165161229-165161442	NONHSAT115989
14	lnc-C6orf118-1	chr6:165219185-165219218	XLOC_005915
15	lnc-C6orf118-1	chr6:165218445-165218579	NONHSAT115991
16	lnc-QKI-4	chr6:165243009-165243106	NONHSAT115993
17	lnc-C6orf118-1	chr6:165218445-165218579	XLOC_005915
18	lnc-C6orf118-1	chr6:165206864-165207641	XLOC_005915
19	lnc-C6orf118-5	chr6:165126854-165127631	ucscGeneNc_uc003qul_1
20	lnc-C6orf118-1	chr6:165241067-165241153	XLOC_005915
21	lnc-QKI-4	chr6:165241259-165241452	NONHSAT115996
22	lnc-C6orf118-1	chr6:165235427-165235542	XLOC_005915
23	lnc-C6orf118-1	chr6:165241067-165241138	NONHSAT115991
24	lnc-QKI-4	chr6:165241239-165241452	XLOC_005533

No data

Variant related genes	Relation type
ENSG00000227455	TF binding region
ENSG00000227455	CpG island
ENSG00000145808	chromatin interactions

Extended variants
information (count: 3428 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3428 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9365732	chr6:165017873-165017874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147829470	chr6:165017928-165017929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534777874	chr6:165017974-165017975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138713012	chr6:165018011-165018012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114012871	chr6:165018044-165018045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs28392513	chr6:165018172-165018173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537148378	chr6:165018191-165018192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs66869416	chr6:165018192-165018193	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs115856753	chr6:165018231-165018232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141591358	chr6:165018340-165018341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190016695	chr6:165018367-165018368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554908670	chr6:165018398-165018399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116474508	chr6:165018404-165018405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76679793	chr6:165018555-165018556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180809875	chr6:165018562-165018563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549152650	chr6:165018577-165018578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186205422	chr6:165018585-165018586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368401957	chr6:165018610-165018611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543887319	chr6:165018625-165018626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563539404	chr6:165018722-165018723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4709867	chr6:165018743-165018744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs71569462	chr6:165018822-165018823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566016199	chr6:165018864-165018865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566354335	chr6:165018897-165018898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551335097	chr6:165018898-165018899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571411645	chr6:165018983-165018984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536756528	chr6:165019034-165019035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369044192	chr6:165019039-165019040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550254450	chr6:165019070-165019071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375341974	chr6:165019085-165019086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556971091	chr6:165019163-165019164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567172523	chr6:165019222-165019223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571511529	chr6:165019231-165019232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141636078	chr6:165019253-165019254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150517820	chr6:165019307-165019308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141022138	chr6:165019310-165019311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541320978	chr6:165019336-165019337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140076784	chr6:165019369-165019370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558107824	chr6:165019372-165019373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578090579	chr6:165019391-165019392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543553535	chr6:165019395-165019396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9459155	chr6:165019416-165019417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs529393446	chr6:165019417-165019418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144968312	chr6:165019421-165019422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559782893	chr6:165019429-165019430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528436905	chr6:165019435-165019436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551612737	chr6:165019450-165019451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9295284	chr6:165019495-165019496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147499135	chr6:165019498-165019499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543923076	chr6:165019516-165019517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165017000-165020600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:165029000-165029400	Enhancers	Brain Germinal Matrix	brain
3	chr6:165029400-165029800	Weak transcription	Brain Germinal Matrix	brain
4	chr6:165029800-165030600	Enhancers	Brain Germinal Matrix	brain
5	chr6:165031000-165031800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:165033000-165033200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:165033200-165033800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:165033400-165034600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:165033800-165034000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:165033800-165039000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:165039000-165039200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:165039800-165040200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:165039800-165041200	Enhancers	Brain Substantia Nigra	brain
14	chr6:165040000-165040800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:165040000-165040800	Enhancers	Brain Hippocampus Middle	brain
16	chr6:165040800-165043000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:165043000-165043600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:165050800-165051000	Enhancers	Brain Anterior Caudate	brain
19	chr6:165051000-165051400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:165051000-165051400	Active TSS	Brain Anterior Caudate	brain
21	chr6:165051000-165051400	Enhancers	Fetal Heart	heart
22	chr6:165051200-165051400	Enhancers	Pancreas	Pancrea
23	chr6:165051400-165052400	Weak transcription	Pancreas	Pancrea
24	chr6:165052400-165052600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:165052400-165052600	Enhancers	Pancreas	Pancrea
26	chr6:165061400-165063000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:165061800-165062000	Enhancers	Brain Hippocampus Middle	brain
28	chr6:165061800-165062400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:165061800-165062400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr6:165061800-165062400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:165061800-165062600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:165062000-165062200	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr6:165062000-165062200	Enhancers	Brain Substantia Nigra	brain
34	chr6:165062000-165062400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr6:165062000-165062400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:165062000-165062400	Enhancers	Adipose Nuclei	Adipose
37	chr6:165062000-165062400	Enhancers	Brain Angular Gyrus	brain
38	chr6:165062000-165062400	Active TSS	Brain Anterior Caudate	brain
39	chr6:165062000-165062400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr6:165062000-165062600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr6:165062000-165062600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr6:165062000-165062600	Enhancers	Brain Germinal Matrix	brain
43	chr6:165062000-165062600	Flanking Active TSS	Brain Hippocampus Middle	brain
44	chr6:165062200-165062400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
45	chr6:165062400-165062600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:165066000-165066400	Enhancers	Aorta	Aorta
47	chr6:165072400-165073000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:165080400-165081000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:165080600-165081200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:165081800-165083000	Enhancers	Fetal Brain Male	brain

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