Variant report

Variant	nsv432983
Chromosome Location	chr6:165554403-165851585
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	chr6:165816575-165816822	MCF-7	breast:	n/a	n/a
7	CEBPB	chr6:165818130-165818440	IMR90	lung:	n/a	chr6:165818295-165818306 chr6:165818293-165818306
8	CEBPB	chr6:165641184-165641536	IMR90	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
9	CEBPB	chr6:165595660-165595860	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:165641185-165641522	HepG2	liver:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
11	CEBPB	chr6:165804346-165804620	HepG2	liver:	n/a	chr6:165804499-165804512 chr6:165804501-165804512 chr6:165804499-165804512 chr6:165804499-165804510
12	CEBPB	chr6:165804332-165804664	IMR90	lung:	n/a	chr6:165804499-165804512 chr6:165804501-165804512 chr6:165804499-165804512 chr6:165804499-165804510
13	CEBPB	chr6:165645810-165646083	HepG2	liver:	n/a	chr6:165645949-165645960
14	CEBPB	chr6:165595689-165595865	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:165556460-165556793	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:165673289-165673478	Hela-S3	cervix:	n/a	chr6:165673335-165673346
17	CEBPB	chr6:165568950-165569240	A549	lung:	n/a	chr6:165569062-165569073
18	CEBPB	chr6:165801165-165801373	A549	lung:	n/a	chr6:165801232-165801243
19	CEBPB	chr6:165630086-165630271	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:165674003-165674256	A549	lung:	n/a	chr6:165674134-165674145
21	CEBPB	chr6:165572815-165572909	H1-hESC	embryonic stem cell:	n/a	chr6:165572819-165572830 chr6:165572819-165572830 chr6:165572819-165572832 chr6:165572819-165572832
22	CEBPB	chr6:165673976-165674309	IMR90	lung:	n/a	chr6:165674134-165674145
23	CEBPB	chr6:165630165-165630323	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:165673285-165673494	HepG2	liver:	n/a	chr6:165673335-165673346
25	CEBPB	chr6:165556474-165556739	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:165801074-165801328	HepG2	liver:	n/a	chr6:165801232-165801243
27	CEBPB	chr6:165810228-165810513	HepG2	liver:	n/a	chr6:165810323-165810334
28	CEBPB	chr6:165641158-165641506	Hela-S3	cervix:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
29	CEBPB	chr6:165673958-165674298	HepG2	liver:	n/a	chr6:165674134-165674145
30	CEBPB	chr6:165641184-165641505	A549	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
31	CEBPB	chr6:165568927-165569218	HepG2	liver:	n/a	chr6:165569062-165569073
32	CHD2	chr6:165722731-165723055	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr6:165722861-165723245	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr6:165606247-165606365	LNCaP	prostate:	n/a	chr6:165606294-165606312 chr6:165606289-165606310
35	CTCF	chr6:165659000-165659150	HUVEC	blood vessel:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
36	CTCF	chr6:165645320-165645470	GM12873	blood:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
37	CTCF	chr6:165642820-165642970	MCF-7	breast:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
38	CTCF	chr6:165659013-165659119	Lung_OC	lung:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
39	CTCF	chr6:165658940-165659090	HA-sp	spinal cord:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
40	CTCF	chr6:165645320-165645470	AoAF	blood vessel:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
41	CTCF	chr6:165645240-165645390	BJ	skin:	n/a	n/a
42	CTCF	chr6:165696944-165696988	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:165835867-165835913	GM19239	blood:	n/a	n/a
44	CTCF	chr6:165645320-165645470	HPAF	blood vessel:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410
45	CTCF	chr6:165658980-165659130	HRPEpiC	eye:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
46	CTCF	chr6:165642860-165643010	K562	blood:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
47	CTCF	chr6:165658964-165659151	MCF-7	breast:	n/a	chr6:165659045-165659063 chr6:165659040-165659061
48	CTCF	chr6:165802547-165802630	ProgFib	skin:	n/a	n/a
49	CTCF	chr6:165642800-165642950	WERI-Rb-1	eye:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
50	CTCF	chr6:165645320-165645470	GM12875	blood:	n/a	chr6:165645393-165645409 chr6:165645387-165645408 chr6:165645392-165645410

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165747029-165747079	ECC-1	luminal epithelium:	n/a
2	chr6:165658423-165658473	ovcar-3	ovarian:	n/a
3	chr6:165722858-165722908	HEK293	kidney:	embryo
4	chr6:165747774-165747824	HCM	heart:	n/a
5	chr6:165747945-165747995	RPTEC	kidney:	n/a
6	chr6:165723708-165723758	U87	brain:	n/a
7	chr6:165715757-165715807	HEK293	kidney:	embryo
8	chr6:165679873-165679923	GM12891	blood:	n/a
9	chr6:165715757-165715807	GM06990	blood:	n/a
10	chr6:165746952-165747002	HUVEC	blood vessel:	n/a
11	chr6:165658423-165658473	A549	lung:	n/a
12	chr6:165658423-165658473	K562	blood:	n/a
13	chr6:165723796-165723846	ECC-1	luminal epithelium:	n/a
14	chr6:165723708-165723758	HRCEpiC	kidney:	n/a
15	chr6:165723034-165723084	SK-N-SH_RA	brain:	n/a
16	chr6:165723708-165723758	GM12878	blood:	n/a
17	chr6:165747969-165748019	BE2_C	brain:	n/a
18	chr6:165746952-165747002	PFSK-1	brain:	n/a
19	chr6:165715586-165715636	HMEC	breast:	n/a
20	chr6:165714794-165714844	K562	blood:	n/a
21	chr6:165715240-165715290	HCM	heart:	n/a
22	chr6:165831916-165831966	PrEC	prostate:	n/a
23	chr6:165747774-165747824	LNCaP	prostate:	n/a
24	chr6:165715586-165715636	Hela-S3	cervix:	n/a
25	chr6:165679873-165679923	HCF	heart:	n/a
26	chr6:165715586-165715636	SK-N-SH	brain:	n/a
27	chr6:165722651-165722701	SK-N-SH_RA	brain:	n/a
28	chr6:165715757-165715807	HMEC	breast:	n/a
29	chr6:165723796-165723846	HRPEpiC	eye:	n/a
30	chr6:165715757-165715807	GM12878	blood:	n/a
31	chr6:165723796-165723846	SK-N-SH_RA	brain:	n/a
32	chr6:165747029-165747079	GM12878	blood:	n/a
33	chr6:165747774-165747824	ProgFib	skin:	n/a
34	chr6:165746952-165747002	RPTEC	kidney:	n/a
35	chr6:165714794-165714844	U87	brain:	n/a
36	chr6:165679873-165679923	HEEpiC	esophagus:	n/a
37	chr6:165831916-165831966	ovcar-3	ovarian:	n/a
38	chr6:165747945-165747995	NH-A	brain:	n/a
39	chr6:165831898-165831948	GM12891	blood:	n/a
40	chr6:165722651-165722701	HEK293	kidney:	embryo
41	chr6:165749446-165749496	NHDF-neo	bronchial:	n/a
42	chr6:165831935-165831985	H1-hESC	embryonic stem cell:	embryo
43	chr6:165724355-165724405	PFSK-1	brain:	n/a
44	chr6:165747774-165747824	HRCEpiC	kidney:	n/a
45	chr6:165747029-165747079	GM19239	blood:	n/a
46	chr6:165723796-165723846	T-47D	breast:	n/a
47	chr6:165722651-165722701	Hepatocyte	liver:	n/a
48	chr6:165749446-165749496	K562	blood:	n/a
49	chr6:165714794-165714844	GM12878	blood:	n/a
50	chr6:165714960-165715010	HL-60	blood:	n/a

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

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

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

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

Extended variants
information (count: 10482 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:10482 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2675731	chr6:165554403-165554404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188830069	chr6:165554438-165554439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534227721	chr6:165554453-165554454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12207165	chr6:165554540-165554541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs13214659	chr6:165554565-165554566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs145779767	chr6:165554571-165554572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556753055	chr6:165554589-165554590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139300437	chr6:165554595-165554596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545711539	chr6:165554641-165554642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528864167	chr6:165554656-165554657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529994556	chr6:165554695-165554696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141908120	chr6:165554723-165554724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572732698	chr6:165554725-165554726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147086027	chr6:165554731-165554732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78280527	chr6:165554752-165554753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528938414	chr6:165554775-165554776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543914770	chr6:165554783-165554784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562335005	chr6:165554789-165554790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114971289	chr6:165554810-165554811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551240220	chr6:165554811-165554812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549010222	chr6:165554828-165554829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs36008116	chr6:165554837-165554838	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs560469434	chr6:165554839-165554840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527442243	chr6:165554898-165554899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538276628	chr6:165555001-165555002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138291243	chr6:165555089-165555090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538327538	chr6:165555091-165555092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191768811	chr6:165555124-165555125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571845126	chr6:165555144-165555145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552350749	chr6:165555146-165555147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535337162	chr6:165555154-165555155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1441900	chr6:165555202-165555203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs572672776	chr6:165555205-165555206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75575509	chr6:165555238-165555239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555305654	chr6:165555249-165555250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573596111	chr6:165555288-165555289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183059157	chr6:165555303-165555304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538374830	chr6:165555319-165555320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34297207	chr6:165555323-165555324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149982935	chr6:165555332-165555333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77109493	chr6:165555333-165555334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144271562	chr6:165555335-165555336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537507479	chr6:165555343-165555344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186982611	chr6:165555377-165555378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544776805	chr6:165555423-165555424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73031121	chr6:165555424-165555425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs13218691	chr6:165555434-165555435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549047654	chr6:165555462-165555463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13217976	chr6:165555556-165555557	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191526365	chr6:165555566-165555567	Weak transcription	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:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165549200-165556000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:165556000-165556400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:165556400-165557000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:165557000-165558000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:165558000-165558600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:165558400-165558800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:165558600-165559400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:165558800-165559000	Enhancers	Brain Substantia Nigra	brain
9	chr6:165558800-165559600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:165559000-165560000	Weak transcription	Brain Substantia Nigra	brain
11	chr6:165559400-165561400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:165559600-165561000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr6:165559600-165562000	Enhancers	Brain Hippocampus Middle	brain
14	chr6:165560000-165560400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:165560000-165560800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr6:165560000-165561600	Enhancers	Brain Substantia Nigra	brain
17	chr6:165560200-165560600	Enhancers	Fetal Muscle Trunk	muscle
18	chr6:165560200-165560600	Enhancers	Fetal Muscle Leg	muscle
19	chr6:165560200-165561200	Enhancers	Brain Cingulate Gyrus	brain
20	chr6:165560400-165560800	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr6:165561400-165570400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:165565400-165567800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:165566400-165566600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:165570400-165571000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr6:165571000-165576200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:165572600-165573400	Enhancers	Fetal Brain Female	brain
27	chr6:165572800-165573800	Enhancers	Fetal Heart	heart
28	chr6:165573200-165573400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:165573800-165574200	Weak transcription	Fetal Heart	heart
30	chr6:165574200-165575400	Enhancers	Fetal Heart	heart
31	chr6:165574800-165575200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:165575200-165575800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:165575800-165576000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:165576000-165576400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:165576200-165578800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:165576400-165577400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:165576600-165577200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:165576800-165577400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:165578800-165587800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:165585800-165586600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:165585800-165591800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:165587800-165589000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:165588400-165589000	ZNF genes & repeats	HSMM	muscle
44	chr6:165589000-165590200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:165589000-165590600	Weak transcription	HSMM	muscle
46	chr6:165590200-165591200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:165590400-165591800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:165590400-165592800	Enhancers	HMEC	breast
49	chr6:165590600-165592400	Enhancers	HSMM	muscle
50	chr6:165591000-165592000	Enhancers	A549	lung

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