Variant report

Variant	nsv432982
Chromosome Location	chr6:165528589-165835589
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	ATF1	chr6:165711237-165711322	K562	blood:	n/a	n/a
2	BACH1	chr6:165804063-165804209	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:165639608-165639621	K562	blood:	n/a	n/a
4	BRCA1	chr6:165755870-165755899	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr6:165734725-165734917	K562	blood:	n/a	n/a
6	CEBPB	chr6:165641184-165641536	IMR90	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
7	CEBPB	chr6:165673976-165674309	IMR90	lung:	n/a	chr6:165674134-165674145
8	CEBPB	chr6:165673958-165674298	HepG2	liver:	n/a	chr6:165674134-165674145
9	CEBPB	chr6:165568927-165569218	HepG2	liver:	n/a	chr6:165569062-165569073
10	CEBPB	chr6:165630165-165630323	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:165816575-165816822	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:165568950-165569240	A549	lung:	n/a	chr6:165569062-165569073
13	CEBPB	chr6:165595660-165595860	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:165818130-165818440	IMR90	lung:	n/a	chr6:165818295-165818306 chr6:165818293-165818306
15	CEBPB	chr6:165801074-165801328	HepG2	liver:	n/a	chr6:165801232-165801243
16	CEBPB	chr6:165801165-165801373	A549	lung:	n/a	chr6:165801232-165801243
17	CEBPB	chr6:165556460-165556793	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:165641185-165641522	HepG2	liver:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
19	CEBPB	chr6:165804346-165804620	HepG2	liver:	n/a	chr6:165804499-165804512 chr6:165804501-165804512 chr6:165804499-165804512 chr6:165804499-165804510
20	CEBPB	chr6:165630086-165630271	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:165673289-165673478	Hela-S3	cervix:	n/a	chr6:165673335-165673346
22	CEBPB	chr6:165804332-165804664	IMR90	lung:	n/a	chr6:165804499-165804512 chr6:165804501-165804512 chr6:165804499-165804512 chr6:165804499-165804510
23	CEBPB	chr6:165556474-165556739	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:165595689-165595865	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:165533080-165533415	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr6:165533000-165533478	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr6:165645810-165646083	HepG2	liver:	n/a	chr6:165645949-165645960
28	CEBPB	chr6:165641184-165641505	A549	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
29	CEBPB	chr6:165674003-165674256	A549	lung:	n/a	chr6:165674134-165674145
30	CEBPB	chr6:165641158-165641506	Hela-S3	cervix:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
31	CEBPB	chr6:165810228-165810513	HepG2	liver:	n/a	chr6:165810323-165810334
32	CEBPB	chr6:165673285-165673494	HepG2	liver:	n/a	chr6:165673335-165673346
33	CEBPB	chr6:165572815-165572909	H1-hESC	embryonic stem cell:	n/a	chr6:165572819-165572830 chr6:165572819-165572830 chr6:165572819-165572832 chr6:165572819-165572832
34	CHD2	chr6:165722861-165723245	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr6:165722731-165723055	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr6:165658668-165659328	SK-N-SH	brain:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
37	CTCF	chr6:165645300-165645450	HVMF	connective:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
38	CTCF	chr6:165645296-165645453	SK-N-SH_RA	brain:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
39	CTCF	chr6:165645340-165645490	AoAF	blood vessel:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
40	CTCF	chr6:165606300-165606450	AG09309	skin:	n/a	n/a
41	CTCF	chr6:165645200-165645350	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr6:165606200-165606350	WERI-Rb-1	eye:	n/a	chr6:165606294-165606312 chr6:165606289-165606310
43	CTCF	chr6:165658980-165659130	HCPEpiC	choroid plexus:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
44	CTCF	chr6:165658984-165659119	HepG2	liver:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
45	CTCF	chr6:165645102-165645601	SK-N-SH	brain:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
46	CTCF	chr6:165645249-165645550	Medullo	brain:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
47	CTCF	chr6:165642800-165642950	AG04449	skin:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
48	CTCF	chr6:165658760-165658910	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:165645280-165645430	NHEK	skin:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
50	CTCF	chr6:165658711-165659422	A549	lung:	n/a	chr6:165659045-165659063 chr6:165659040-165659061

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165723796-165723846	PFSK-1	brain:	n/a
2	chr6:165831916-165831966	ECC-1	luminal epithelium:	n/a
3	chr6:165747774-165747824	NH-A	brain:	n/a
4	chr6:165723796-165723846	PFSK-1	brain:	n/a
5	chr6:165831916-165831966	ECC-1	luminal epithelium:	n/a
6	chr6:165747774-165747824	NH-A	brain:	n/a
7	chr6:165749446-165749496	HCPEpiC	choroid plexus:	n/a
8	chr6:165723708-165723758	NB4	blood:	n/a
9	chr6:165715586-165715636	GM12892	blood:	n/a
10	chr6:165746952-165747002	T-47D	breast:	n/a
11	chr6:165747945-165747995	SKMC	muscle:	n/a
12	chr6:165723034-165723084	GM12892	blood:	n/a
13	chr6:165715240-165715290	GM12891	blood:	n/a
14	chr6:165831916-165831966	RPTEC	kidney:	n/a
15	chr6:165715757-165715807	NHDF-neo	bronchial:	n/a
16	chr6:165722858-165722908	AoSMC	blood vessel:	n/a
17	chr6:165722858-165722908	HL-60	blood:	n/a
18	chr6:165723708-165723758	U87	brain:	n/a
19	chr6:165715757-165715807	SKMC	muscle:	n/a
20	chr6:165747945-165747995	NB4	blood:	n/a
21	chr6:165715240-165715290	PrEC	prostate:	n/a
22	chr6:165723034-165723084	HCPEpiC	choroid plexus:	n/a
23	chr6:165715586-165715636	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:165722651-165722701	U87	brain:	n/a
25	chr6:165723796-165723846	CMK	blood:	n/a
26	chr6:165723796-165723846	HEEpiC	esophagus:	n/a
27	chr6:165714794-165714844	NT2-D1	testis:	n/a
28	chr6:165715586-165715636	AG04450	lung:	fetal
29	chr6:165831898-165831948	U87	brain:	n/a
30	chr6:165747969-165748019	AG09309	skin:	n/a
31	chr6:165714794-165714844	HEEpiC	esophagus:	n/a
32	chr6:165722651-165722701	Hepatocyte	liver:	n/a
33	chr6:165714794-165714844	AG09319	gingival:	n/a
34	chr6:165715240-165715290	AG09319	gingival:	n/a
35	chr6:165715592-165715642	AoSMC	blood vessel:	n/a
36	chr6:165831935-165831985	ECC-1	luminal epithelium:	n/a
37	chr6:165723034-165723084	SK-N-SH_RA	brain:	n/a
38	chr6:165722858-165722908	HRE	kidney:	n/a
39	chr6:165715240-165715290	BE2_C	brain:	n/a
40	chr6:165723708-165723758	NT2-D1	testis:	n/a
41	chr6:165658423-165658473	BJ	skin:	n/a
42	chr6:165723034-165723084	Jurkat	blood:	n/a
43	chr6:165722858-165722908	NHDF-neo	bronchial:	n/a
44	chr6:165722651-165722701	NH-A	brain:	n/a
45	chr6:165715586-165715636	LNCaP	prostate:	n/a
46	chr6:165714960-165715010	HMEC	breast:	n/a
47	chr6:165679873-165679923	BJ	skin:	n/a
48	chr6:165749446-165749496	NHDF-neo	bronchial:	n/a
49	chr6:165679873-165679923	HCPEpiC	choroid plexus:	n/a
50	chr6:165747969-165748019	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
2	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
3	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
4	chr6:165746371..165749114-chr6:165759117..165761315,2	MCF-7	breast:
5	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
6	chr6:165828345..165831277-chr6:165841740..165844002,2	K562	blood:
7	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
8	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
9	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
10	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:
11	chr6:165693401..165693973-chr6:165739529..165740029,2	K562	blood:
12	chr6:165641887..165643835-chr6:165647824..165649680,2	K562	blood:
13	chr6:165693401..165693973-chr6:165739529..165740029,2	K562	blood:
14	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
15	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
16	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
17	chr6:165641887..165643835-chr6:165647824..165649680,2	K562	blood:
18	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
19	chr6:165746371..165749114-chr6:165759117..165761315,2	MCF-7	breast:
20	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
21	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-3	chr6:165695129-165695184	NONHSAT116000
2	lnc-SDIM1-2	chr6:165740975-165742467	NONHSAT116002
3	lnc-C6orf118-3	chr6:165693522-165693599	NONHSAT116001
4	lnc-C6orf118-4	chr6:165530684-165531013	NONHSAT115999
5	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116000
6	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116001
7	lnc-C6orf118-3	chr6:165693153-165693522	NONHSAT116000
8	lnc-C6orf118-3	chr6:165695129-165695511	NONHSAT116001

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf118	hsa-miR-1	chr6:165693446-165693473

Variant related genes	Relation type
C6orf118	TF binding region
ENSG00000217878	TF binding region
RNA5SP226	TF binding region
C6orf118	CpG island
ENSG00000217878	CpG island
RNA5SP226	CpG island

Extended variants
information (count: 10645 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:10645 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147119663	chr6:165528647-165528648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568177046	chr6:165528696-165528697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189706005	chr6:165528725-165528726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138572186	chr6:165528762-165528763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143976919	chr6:165528772-165528773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180882993	chr6:165528801-165528802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540414896	chr6:165528807-165528808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73255517	chr6:165528815-165528816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs73255520	chr6:165528828-165528829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185236257	chr6:165528844-165528845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2758933	chr6:165528860-165528861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114745897	chr6:165528861-165528862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551791272	chr6:165528991-165528992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144360004	chr6:165529009-165529010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576280757	chr6:165529067-165529068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534054840	chr6:165529080-165529081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549087362	chr6:165529082-165529083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188196694	chr6:165529196-165529197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73255522	chr6:165529230-165529231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556533355	chr6:165529275-165529276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148743199	chr6:165529290-165529291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181727666	chr6:165529332-165529333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555895017	chr6:165529347-165529348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56103689	chr6:165529354-165529355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186351426	chr6:165529377-165529378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541639797	chr6:165529399-165529400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559978927	chr6:165529401-165529402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561772654	chr6:165529411-165529412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573705728	chr6:165529499-165529500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190363842	chr6:165529507-165529508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114776920	chr6:165529568-165529569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183575025	chr6:165529595-165529596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186417839	chr6:165529661-165529662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560087105	chr6:165529682-165529683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55974039	chr6:165529732-165529733	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191358129	chr6:165529777-165529778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182787361	chr6:165529784-165529785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550392342	chr6:165529821-165529822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571834580	chr6:165529822-165529823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539349367	chr6:165529852-165529853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373165499	chr6:165529891-165529892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186622465	chr6:165529894-165529895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191519982	chr6:165529895-165529896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545813912	chr6:165529906-165529907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533770303	chr6:165529911-165529912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555496401	chr6:165529926-165529927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573719132	chr6:165529990-165529991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113355211	chr6:165530040-165530041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183272221	chr6:165530070-165530071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139535604	chr6:165530071-165530072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165516400-165530800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:165520600-165529800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr6:165528400-165528600	ZNF genes & repeats	Psoas Muscle	Psoas
4	chr6:165529400-165533600	Enhancers	HSMM	muscle
5	chr6:165529800-165530600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr6:165530200-165533400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:165530400-165530600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:165530600-165531000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr6:165530600-165531800	Enhancers	HSMMtube	muscle
10	chr6:165530800-165531600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:165530800-165532600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:165531000-165531200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr6:165531200-165532400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr6:165531600-165532800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:165531800-165532200	Weak transcription	HSMMtube	muscle
16	chr6:165532200-165533600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:165532200-165533600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:165532200-165533600	Enhancers	HSMMtube	muscle
19	chr6:165532400-165533400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:165532400-165533400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:165532400-165533600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:165532400-165533600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:165532400-165533600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr6:165532400-165533600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:165532400-165533600	Enhancers	Osteobl	bone
26	chr6:165532600-165532800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr6:165532600-165533600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:165532600-165533600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:165532600-165533800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:165532800-165533400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:165532800-165533600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:165532800-165533600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:165532800-165533800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:165532800-165533800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr6:165533000-165533600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:165533000-165533600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:165533200-165533400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:165533200-165533600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr6:165533200-165533600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:165533400-165533600	Enhancers	H9 Cell Line	embryonic stem cell
41	chr6:165533600-165537200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:165539200-165540200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:165542200-165543000	Enhancers	Brain Germinal Matrix	brain
44	chr6:165543000-165543600	Weak transcription	Brain Germinal Matrix	brain
45	chr6:165543600-165543800	Enhancers	Brain Germinal Matrix	brain
46	chr6:165548600-165549200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:165549200-165556000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:165549800-165550000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:165550000-165551000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:165556000-165556400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin

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