Variant report

Variant	nsv604781
Chromosome Location	chr6:141165191-141219060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:368)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:141178980-141179277	K562	blood:	n/a	n/a
2	ATF1	chr6:141218607-141218807	K562	blood:	n/a	n/a
3	BATF	chr6:141179510-141179919	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:141179621-141179991	K562	blood:	n/a	n/a
5	BHLHE40	chr6:141218694-141218754	K562	blood:	n/a	n/a
6	BHLHE40	chr6:141178965-141179291	K562	blood:	n/a	n/a
7	CEBPB	chr6:141168086-141168341	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:141178889-141179901	Hela-S3	cervix:	n/a	chr6:141179299-141179310 chr6:141178917-141178930 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
9	CEBPB	chr6:141179179-141179486	A549	lung:	n/a	chr6:141179299-141179310 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
10	CEBPB	chr6:141201080-141201395	HepG2	liver:	n/a	chr6:141201226-141201237
11	CEBPB	chr6:141168022-141168392	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:141200929-141201437	A549	lung:	n/a	chr6:141201226-141201237
13	CEBPB	chr6:141201024-141201417	A549	lung:	n/a	chr6:141201226-141201237
14	CEBPB	chr6:141201069-141201388	A549	lung:	n/a	chr6:141201226-141201237
15	CEBPB	chr6:141201058-141201444	Hela-S3	cervix:	n/a	chr6:141201226-141201237
16	CEBPB	chr6:141178787-141179735	IMR90	lung:	n/a	chr6:141179299-141179310 chr6:141178917-141178930 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
17	CEBPB	chr6:141217203-141217479	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:141218515-141218842	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:141218598-141218858	K562	blood:	n/a	n/a
20	CEBPB	chr6:141201023-141201414	IMR90	lung:	n/a	chr6:141201226-141201237
21	CEBPB	chr6:141179182-141179506	HepG2	liver:	n/a	chr6:141179299-141179310 chr6:141179300-141179311 chr6:141179299-141179312 chr6:141179299-141179312 chr6:141179299-141179310 chr6:141179357-141179368
22	CHD1	chr6:141219020-141219220	GM12878	blood:	n/a	n/a
23	CHD2	chr6:141218709-141218874	GM12878	blood:	n/a	n/a
24	CTCF	chr6:141185884-141185940	GM20000	blood:	n/a	n/a
25	CTCF	chr6:141179020-141179170	HMF	breast:	n/a	n/a
26	CTCF	chr6:141179020-141179170	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr6:141179040-141179190	HPF	lung:	n/a	n/a
28	CTCF	chr6:141214880-141215030	NB4	blood:	n/a	n/a
29	CTCF	chr6:141214900-141215050	HCT-116	colon:	n/a	n/a
30	CTCF	chr6:141214680-141214830	HCT-116	colon:	n/a	n/a
31	CTCF	chr6:141179020-141179170	HCM	heart:	n/a	n/a
32	CTCF	chr6:141179000-141179150	AG04449	skin:	n/a	n/a
33	CTCF	chr6:141178920-141179070	BJ	skin:	n/a	n/a
34	CTCF	chr6:141179000-141179150	HPF	lung:	n/a	n/a
35	CTCF	chr6:141178980-141179130	AG10803	skin:	n/a	n/a
36	CTCF	chr6:141214860-141215010	GM12874	blood:	n/a	n/a
37	CTCF	chr6:141179000-141179150	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr6:141214860-141215010	HEK293	kidney:	n/a	n/a
39	CTCF	chr6:141178940-141179090	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr6:141214840-141214990	HepG2	liver:	n/a	n/a
41	CTCF	chr6:141178920-141179070	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr6:141180819-141180841	GM13977	blood:	n/a	n/a
43	CTCF	chr6:141179020-141179170	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr6:141179060-141179210	HMF	breast:	n/a	n/a
45	CTCF	chr6:141214793-141215010	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:141178960-141179110	AG10803	skin:	n/a	n/a
47	CTCF	chr6:141178920-141179190	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr6:141178980-141179130	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr6:141178940-141179090	HCFaa	heart:	n/a	n/a
50	E2F4	chr6:141178909-141179859	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141167819-141167869	HUVEC	blood vessel:	n/a
2	chr6:141167819-141167869	ProgFib	skin:	n/a
3	chr6:141167819-141167869	AG09309	skin:	n/a
4	chr6:141167819-141167869	LNCaP	prostate:	n/a
5	chr6:141167819-141167869	GM12878	blood:	n/a
6	chr6:141167819-141167869	H1-hESC	embryonic stem cell:	embryo
7	chr6:141167819-141167869	HCPEpiC	choroid plexus:	n/a
8	chr6:141167819-141167869	SK-N-SH_RA	brain:	n/a
9	chr6:141167819-141167869	PANC-1	pancreas:	n/a
10	chr6:141167819-141167869	GM12891	blood:	n/a
11	chr6:141167819-141167869	MCF10A-Er-Src	breast:	n/a
12	chr6:141167819-141167869	U87	brain:	n/a
13	chr6:141167819-141167869	HIPEpiC	eye:	n/a
14	chr6:141167819-141167869	SK-N-SH	brain:	n/a
15	chr6:141167819-141167869	SAEC	small airway:	n/a
16	chr6:141167819-141167869	HCT-116	colon:	n/a
17	chr6:141167819-141167869	AoSMC	blood vessel:	n/a
18	chr6:141167819-141167869	T-47D	breast:	n/a
19	chr6:141167819-141167869	NH-A	brain:	n/a
20	chr6:141167819-141167869	HepG2	liver:	n/a
21	chr6:141167819-141167869	HCM	heart:	n/a
22	chr6:141167819-141167869	GM19239	blood:	n/a
23	chr6:141167819-141167869	GM06990	blood:	n/a
24	chr6:141167819-141167869	HL-60	blood:	n/a
25	chr6:141167819-141167869	PrEC	prostate:	n/a
26	chr6:141167819-141167869	HAEpiC	amniotic membrane:	n/a
27	chr6:141167819-141167869	NT2-D1	testis:	n/a
28	chr6:141167819-141167869	ovcar-3	ovarian:	n/a
29	chr6:141167819-141167869	PFSK-1	brain:	n/a
30	chr6:141167819-141167869	AG04450	lung:	fetal
31	chr6:141167819-141167869	HRE	kidney:	n/a
32	chr6:141167819-141167869	BJ	skin:	n/a
33	chr6:141167819-141167869	NB4	blood:	n/a
34	chr6:141167819-141167869	ECC-1	luminal epithelium:	n/a
35	chr6:141167819-141167869	AG09319	gingival:	n/a
36	chr6:141167819-141167869	Hela-S3	cervix:	n/a
37	chr6:141167819-141167869	HEK293	kidney:	embryo
38	chr6:141167819-141167869	AG04449	skin:	fetal
39	chr6:141167819-141167869	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:141167819-141167869	RPTEC	kidney:	n/a
41	chr6:141167819-141167869	HRPEpiC	eye:	n/a
42	chr6:141167819-141167869	BE2_C	brain:	n/a
43	chr6:141167819-141167869	A549	lung:	n/a
44	chr6:141167819-141167869	SK-N-MC	brain:	n/a
45	chr6:141167819-141167869	HRCEpiC	kidney:	n/a
46	chr6:141167819-141167869	MCF-7	breast:	n/a
47	chr6:141167819-141167869	GM12892	blood:	n/a
48	chr6:141167819-141167869	SKMC	muscle:	n/a
49	chr6:141167819-141167869	HMEC	breast:	n/a
50	chr6:141167819-141167869	Caco-2	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
2	chr6:141209671..141212646-chr6:141217346..141220652,3	K562	blood:
3	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
4	chr6:141186030..141188645-chr6:141209021..141211970,2	K562	blood:
5	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
6	chr6:141218727..141221164-chr6:141224854..141227033,2	K562	blood:
7	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:
8	chr6:141212244..141214629-chr6:141219189..141220964,2	MCF-7	breast:
9	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
10	chr6:141210884..141213823-chr6:141384643..141387034,2	K562	blood:
11	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
12	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
13	chr6:141201313..141204931-chr6:141205813..141208687,3	K562	blood:
14	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
15	chr6:141194692..141196921-chr6:141200242..141202633,2	K562	blood:
16	chr6:141194790..141196921-chr6:141201066..141202633,2	K562	blood:
17	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
18	chr6:141201035..141203602-chr6:141204106..141206324,2	MCF-7	breast:
19	chr6:141204507..141206612-chr6:141209189..141212114,2	K562	blood:
20	chr6:141212782..141215020-chr6:141216248..141219853,3	K562	blood:
21	chr6:141203363..141207943-chr6:141209189..141214513,5	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-8	chr6:141208788-141209134	NONHSAT115290
2	lnc-NMBR-2	chr6:141184950-141184976	NONHSAT115288
3	lnc-NMBR-2	chr6:141185039-141185580	NONHSAT115288
4	lnc-NMBR-2	chr6:141167095-141167471	NONHSAT115288
5	lnc-NMBR-2	chr6:141216940-141217067	NONHSAT115288
6	lnc-NMBR-2	chr6:141173956-141174059	NONHSAT115288
7	lnc-NMBR-2	chr6:141167095-141167441	ENSG00000234147
8	lnc-NMBR-8	chr6:141215649-141215754	NONHSAT115290
9	lnc-NMBR-2	chr6:141184986-141185033	NONHSAT115288
10	lnc-NMBR-2	chr6:141173956-141174061	ENSG00000234147

No data

Variant related genes	Relation type
ENSG00000234147	TF binding region
ENSG00000234147	CpG island

Extended variants
information (count: 1929 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs620151	chr6:141165191-141165192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531696375	chr6:141165254-141165255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142797782	chr6:141165282-141165283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569074637	chr6:141165329-141165330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533056077	chr6:141165330-141165331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs71740251	chr6:141165336-141165337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77668308	chr6:141165349-141165350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78380016	chr6:141165350-141165351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs36066105	chr6:141165351-141165352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529843786	chr6:141165368-141165369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147413093	chr6:141165388-141165389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs687879	chr6:141165413-141165414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs533740356	chr6:141165589-141165590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs630596	chr6:141165614-141165615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187800842	chr6:141165620-141165621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536764503	chr6:141165648-141165649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537977991	chr6:141165660-141165661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556789577	chr6:141165675-141165676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551927039	chr6:141165676-141165677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139767650	chr6:141165734-141165735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554413591	chr6:141165739-141165740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572674021	chr6:141165775-141165776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543001103	chr6:141165777-141165778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542567471	chr6:141165780-141165781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190717723	chr6:141165814-141165815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182769246	chr6:141165827-141165828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs582098	chr6:141165880-141165881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs633796	chr6:141165940-141165941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs187841699	chr6:141165950-141165951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551308481	chr6:141166002-141166003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192773735	chr6:141166023-141166024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35930958	chr6:141166048-141166049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527591599	chr6:141166073-141166074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141809286	chr6:141166140-141166141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559214171	chr6:141166170-141166171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567314627	chr6:141166187-141166188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143068334	chr6:141166211-141166212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374922644	chr6:141166213-141166214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150499234	chr6:141166232-141166233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs635096	chr6:141166254-141166255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs571272062	chr6:141166255-141166256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563226507	chr6:141166268-141166269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139464901	chr6:141166316-141166317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149683359	chr6:141166333-141166334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184806394	chr6:141166336-141166337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187874330	chr6:141166338-141166339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576062869	chr6:141166350-141166351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543426192	chr6:141166377-141166378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565350576	chr6:141166410-141166411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs594761	chr6:141166412-141166413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

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
Autism	21448237	CNVD
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141152800-141171600	Weak transcription	Aorta	Aorta
2	chr6:141164800-141166200	Weak transcription	NHLF	lung
3	chr6:141165000-141188400	Weak transcription	HepG2	liver
4	chr6:141166200-141166400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:141166200-141167000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:141166200-141167400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr6:141166200-141167800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:141166200-141168200	Enhancers	NHLF	lung
9	chr6:141166400-141167000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:141166600-141167000	Enhancers	Fetal Heart	heart
11	chr6:141166600-141167600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:141166600-141169200	Enhancers	Osteobl	bone
13	chr6:141166600-141169800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:141166600-141172400	Enhancers	NHDF-Ad	bronchial
15	chr6:141166800-141168200	Enhancers	NH-A	brain
16	chr6:141166800-141169200	Enhancers	Hela-S3	cervix
17	chr6:141166800-141172600	Enhancers	HUVEC	blood vessel
18	chr6:141166800-141173600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:141167000-141170000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:141167200-141167400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:141167200-141168000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr6:141167200-141169800	Enhancers	HSMM	muscle
23	chr6:141167400-141167800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr6:141167400-141167800	Enhancers	HSMMtube	muscle
25	chr6:141167400-141168000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:141167600-141168000	Enhancers	Adipose Nuclei	Adipose
27	chr6:141167600-141168000	Enhancers	A549	lung
28	chr6:141167600-141168200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:141167600-141183000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:141167800-141170400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:141167800-141170800	Weak transcription	HSMMtube	muscle
32	chr6:141167800-141172600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:141168000-141168600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:141168000-141168800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:141168200-141168800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:141168200-141169000	Weak transcription	NHLF	lung
37	chr6:141168200-141171400	Weak transcription	NH-A	brain
38	chr6:141168600-141169200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:141168800-141169000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:141168800-141169000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:141169000-141169200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:141169000-141169200	Enhancers	NHLF	lung
43	chr6:141169000-141169600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:141169200-141169400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:141169200-141169800	Weak transcription	NHLF	lung
46	chr6:141169200-141170400	Weak transcription	Osteobl	bone
47	chr6:141169200-141171400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr6:141169200-141176800	Weak transcription	Hela-S3	cervix
49	chr6:141169400-141173600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:141169600-141169800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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