Variant report

Variant	nsv1025706
Chromosome Location	chr6:141909953-142131906
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:305)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:142024298-142024372	K562	blood:	n/a	n/a
2	ATF1	chr6:142061523-142061667	K562	blood:	n/a	n/a
3	BACH1	chr6:142100214-142100436	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:141955169-141955254	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:142100183-142100479	K562	blood:	n/a	n/a
6	BATF	chr6:142126559-142126818	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:142126780-142126784	GM12878	blood:	n/a	n/a
8	CBX3	chr6:141998805-141999164	HCT-116	colon:	n/a	n/a
9	CBX3	chr6:142103323-142103555	K562	blood:	n/a	n/a
10	CEBPB	chr6:142073912-142074198	Hela-S3	cervix:	n/a	chr6:142074013-142074030 chr6:142074015-142074026
11	CEBPB	chr6:142131124-142131388	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:141981657-141981769	A549	lung:	n/a	n/a
13	CEBPB	chr6:142021970-142022356	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:142044132-142044467	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:141971444-141971684	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:142005498-142005769	HepG2	liver:	n/a	chr6:142005655-142005666
17	CEBPB	chr6:142097651-142097894	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:141989336-141989446	H1-hESC	embryonic stem cell:	n/a	chr6:141989394-141989405
19	CEBPB	chr6:142018377-142018563	HepG2	liver:	n/a	chr6:142018504-142018515
20	CEBPB	chr6:142006477-142006878	IMR90	lung:	n/a	chr6:142006576-142006587
21	CEBPB	chr6:141989304-141989526	HepG2	liver:	n/a	chr6:141989394-141989405
22	CEBPB	chr6:142073891-142074178	HepG2	liver:	n/a	chr6:142074013-142074030 chr6:142074015-142074026
23	CEBPB	chr6:142006422-142006670	HepG2	liver:	n/a	chr6:142006576-142006587
24	CEBPB	chr6:142032958-142033209	HepG2	liver:	n/a	chr6:142033019-142033030
25	CEBPB	chr6:141971422-141971563	A549	lung:	n/a	n/a
26	CEBPB	chr6:142044226-142044293	A549	lung:	n/a	n/a
27	CEBPB	chr6:142046652-142046833	HepG2	liver:	n/a	chr6:142046730-142046741
28	CEBPB	chr6:142061308-142061552	HepG2	liver:	n/a	chr6:142061435-142061446
29	CEBPB	chr6:142040693-142040957	HepG2	liver:	n/a	chr6:142040818-142040827 chr6:142040818-142040827 chr6:142040816-142040827
30	CTCF	chr6:141932060-141932210	HCM	heart:	n/a	chr6:141932125-141932146
31	CTCF	chr6:141932073-141932162	Hela-S3	cervix:	n/a	chr6:141932125-141932146
32	CTCF	chr6:141932040-141932190	Caco-2	colon:	n/a	chr6:141932125-141932146
33	CTCF	chr6:141932120-141932270	WI-38	lung:	n/a	chr6:141932125-141932146
34	CTCF	chr6:141997200-141997350	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr6:141998840-141998990	HMEC	breast:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
36	CTCF	chr6:141919172-141919200	LNCaP	prostate:	n/a	n/a
37	CTCF	chr6:141998869-141998999	Lung_OC	lung:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
38	CTCF	chr6:141998860-141999010	HEK293	kidney:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
39	CTCF	chr6:141997240-141997390	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr6:141998821-141999041	Gliobla	brain:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
41	CTCF	chr6:141998940-141999090	GM12870	blood:	n/a	n/a
42	CTCF	chr6:141998739-141999151	IMR90	lung:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
43	CTCF	chr6:141997200-141997350	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr6:141998840-141998990	HCPEpiC	choroid plexus:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
45	CTCF	chr6:141998728-141999136	A549	lung:	n/a	chr6:141998929-141998945 chr6:141998930-141998951 chr6:141998931-141998944 chr6:141998928-141998946
46	CTCF	chr6:141932060-141932210	MCF-7	breast:	n/a	chr6:141932125-141932146
47	CTCF	chr6:141998680-141998830	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr6:141932100-141932250	HFF-Myc	foreskin:	n/a	chr6:141932125-141932146
49	CTCF	chr6:141916134-141916258	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:141916140-141916290	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142047924-142047974	HEK293	kidney:	embryo
2	chr6:142007733-142007783	NB4	blood:	n/a
3	chr6:142047924-142047974	H1-hESC	embryonic stem cell:	embryo
4	chr6:142129232-142129282	IMR90	lung:	fetal
5	chr6:141939449-141939499	BJ	skin:	n/a
6	chr6:142129232-142129282	HRE	kidney:	n/a
7	chr6:142129232-142129282	HepG2	liver:	n/a
8	chr6:141939449-141939499	A549	lung:	n/a
9	chr6:141939449-141939499	HMEC	breast:	n/a
10	chr6:142047924-142047974	K562	blood:	n/a
11	chr6:142007795-142007845	HRPEpiC	eye:	n/a
12	chr6:142047924-142047974	PFSK-1	brain:	n/a
13	chr6:141939449-141939499	SK-N-SH_RA	brain:	n/a
14	chr6:142007795-142007845	RPTEC	kidney:	n/a
15	chr6:142007733-142007783	A549	lung:	n/a
16	chr6:142007795-142007845	ProgFib	skin:	n/a
17	chr6:142129232-142129282	NB4	blood:	n/a
18	chr6:142047924-142047974	HMEC	breast:	n/a
19	chr6:142047924-142047974	NHDF-neo	bronchial:	n/a
20	chr6:141939449-141939499	PrEC	prostate:	n/a
21	chr6:141939449-141939499	AoSMC	blood vessel:	n/a
22	chr6:142047924-142047974	ProgFib	skin:	n/a
23	chr6:142007733-142007783	GM12878	blood:	n/a
24	chr6:142007733-142007783	SK-N-SH	brain:	n/a
25	chr6:142007795-142007845	AG04449	skin:	fetal
26	chr6:142047924-142047974	Hela-S3	cervix:	n/a
27	chr6:142007733-142007783	AG04449	skin:	fetal
28	chr6:142047924-142047974	HUVEC	blood vessel:	n/a
29	chr6:142007733-142007783	HEEpiC	esophagus:	n/a
30	chr6:142007795-142007845	HEK293	kidney:	embryo
31	chr6:141939449-141939499	HCPEpiC	choroid plexus:	n/a
32	chr6:142007795-142007845	MCF10A-Er-Src	breast:	n/a
33	chr6:141939449-141939499	Hela-S3	cervix:	n/a
34	chr6:142007795-142007845	PANC-1	pancreas:	n/a
35	chr6:142129232-142129282	AG09319	gingival:	n/a
36	chr6:141939449-141939499	CMK	blood:	n/a
37	chr6:142047924-142047974	MCF10A-Er-Src	breast:	n/a
38	chr6:142007795-142007845	AG10803	skin:	n/a
39	chr6:142129232-142129282	T-47D	breast:	n/a
40	chr6:141939449-141939499	Jurkat	blood:	n/a
41	chr6:142047924-142047974	NH-A	brain:	n/a
42	chr6:142129232-142129282	HNPCEpiC	eye:	n/a
43	chr6:142007733-142007783	HEK293	kidney:	embryo
44	chr6:142129232-142129282	HCF	heart:	n/a
45	chr6:142007795-142007845	BE2_C	brain:	n/a
46	chr6:141939449-141939499	H1-hESC	embryonic stem cell:	embryo
47	chr6:142007795-142007845	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:142007733-142007783	HCM	heart:	n/a
49	chr6:142129232-142129282	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:142047924-142047974	GM12878	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:142043541..142046189-chr6:142046868..142049231,2	K562	blood:
2	chr6:141998651..141999214-chr6:142310161..142310947,2	MCF-7	breast:
3	chr6:142124743..142126813-chr6:142127411..142130975,3	K562	blood:
4	chr6:141998709..141999469-chr6:142433501..142434128,2	K562	blood:
5	chr6:141998460..141999421-chr6:142110108..142110780,4	MCF-7	breast:
6	chr6:142050849..142053008-chr6:142057851..142059838,2	MCF-7	breast:
7	chr6:142124743..142126813-chr6:142127411..142130975,3	K562	blood:
8	chr6:142037919..142039728-chr6:142043594..142045386,2	K562	blood:
9	chr6:141998840..141999399-chr6:142365802..142366506,2	MCF-7	breast:
10	chr6:142052857..142055302-chr6:142056890..142059769,2	K562	blood:
11	chr6:142049775..142053768-chr6:142054988..142057417,3	K562	blood:
12	chr6:142009509..142011064-chr6:142029041..142031372,2	K562	blood:
13	chr6:142046394..142048576-chr6:142051294..142053938,2	K562	blood:
14	chr6:142052857..142055302-chr6:142056890..142059769,2	K562	blood:
15	chr6:141980585..141982447-chr6:141983918..141986219,2	K562	blood:
16	chr6:141998460..141999421-chr6:142110108..142110780,4	MCF-7	breast:
17	chr6:142049775..142053768-chr6:142054988..142057417,3	K562	blood:
18	chr6:142037919..142039728-chr6:142043594..142045386,2	K562	blood:
19	chr6:142128195..142130687-chr6:142132309..142133838,2	K562	blood:
20	chr6:142050849..142053008-chr6:142057851..142059838,2	MCF-7	breast:
21	chr6:142043541..142046189-chr6:142046868..142049231,2	K562	blood:
22	chr6:142046394..142048576-chr6:142051294..142053938,2	K562	blood:
23	chr6:141962578..141963250-chr6:142366256..142367149,2	MCF-7	breast:
24	chr6:141996747..141997654-chr6:142433323..142434142,3	MCF-7	breast:
25	chr6:141980585..141982447-chr6:141983918..141986219,2	K562	blood:
26	chr6:141998099..141999007-chr6:142433461..142433965,2	MCF-7	breast:
27	chr6:141998374..141999368-chr6:142433353..142434249,2	MCF-7	breast:
28	chr6:141931693..141932316-chr6:141996864..141997483,2	MCF-7	breast:
29	chr6:142009509..142011064-chr6:142029041..142031372,2	K562	blood:
30	chr22:21982581..21985457-chr6:141960441..141962007,2	K562	blood:
31	chr6:141931693..141932316-chr6:141996864..141997483,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-6	chr6:141956787-141957472	NONHSAT115298
2	lnc-NMBR-6	chr6:141956857-141957640	NONHSAT115299

No data

Variant related genes	Relation type
RPS3AP23	TF binding region
RPS3AP23	CpG island
ENSG00000161179	chromatin interactions

Extended variants
information (count: 3083 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3083 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367876416	chr6:141909981-141909982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377262828	chr6:141910032-141910033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562889035	chr6:141910042-141910043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114285992	chr6:141910100-141910101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185631431	chr6:141910113-141910114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12190658	chr6:141910117-141910118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528413997	chr6:141910169-141910170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143158261	chr6:141910222-141910223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568245256	chr6:141910224-141910225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529142432	chr6:141910235-141910236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190134789	chr6:141910244-141910245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148270941	chr6:141910315-141910316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35251722	chr6:141910317-141910318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141375568	chr6:141910328-141910329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557492535	chr6:141910401-141910402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372828559	chr6:141910405-141910406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147436383	chr6:141910420-141910421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567794648	chr6:141910455-141910456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534206538	chr6:141910475-141910476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555683002	chr6:141910506-141910507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573895896	chr6:141910518-141910519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112431207	chr6:141910519-141910520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182371685	chr6:141910532-141910533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556582625	chr6:141910554-141910555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578043950	chr6:141910575-141910576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs137868045	chr6:141910579-141910580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536637469	chr6:141910604-141910605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143424183	chr6:141910634-141910635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527719165	chr6:141910636-141910637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540523544	chr6:141910701-141910702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187045865	chr6:141910710-141910711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529036804	chr6:141910725-141910726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550518686	chr6:141910728-141910729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191435742	chr6:141910809-141910810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147154026	chr6:141910847-141910848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374668418	chr6:141910912-141910913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551489115	chr6:141910947-141910948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566124546	chr6:141910969-141910970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570075919	chr6:141910987-141910988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201506983	chr6:141910990-141910991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370839559	chr6:141911009-141911010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74805449	chr6:141911044-141911045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539285998	chr6:141911055-141911056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2328260	chr6:141911056-141911057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs112016788	chr6:141911063-141911064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556500458	chr6:141911083-141911084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578142707	chr6:141911091-141911092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184173512	chr6:141911102-141911103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572579783	chr6:141911132-141911133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35335056	chr6:141911161-141911162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141909400-141919600	Weak transcription	NHLF	lung
2	chr6:141911600-141912400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr6:141919200-141919600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr6:141919400-141919800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:141919400-141919800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr6:141919400-141919800	Enhancers	NHDF-Ad	bronchial
7	chr6:141919400-141920000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:141919400-141920200	Enhancers	HUVEC	blood vessel
9	chr6:141919400-141920400	Enhancers	Osteobl	bone
10	chr6:141919600-141919800	Enhancers	NHLF	lung
11	chr6:141920000-141923400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:141920200-141921800	Weak transcription	HUVEC	blood vessel
13	chr6:141921800-141922400	Enhancers	HUVEC	blood vessel
14	chr6:141923400-141924000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:141926400-141928800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:141928600-141929400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:141931800-141932400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:141939200-141939600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr6:141939200-141939800	Active TSS	Placenta	Placenta
20	chr6:141939200-141940000	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr6:141958400-141959000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:141971200-141971600	Enhancers	Fetal Heart	heart
23	chr6:141979600-141980200	Enhancers	NHEK	skin
24	chr6:141984800-141986600	Weak transcription	Psoas Muscle	Psoas
25	chr6:141986600-141986800	Enhancers	Psoas Muscle	Psoas
26	chr6:141987000-141987200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:141987000-141987800	Enhancers	Liver	Liver
28	chr6:141987200-141989200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:141987400-141988600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr6:141988400-141989600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr6:141988400-141989800	Enhancers	HMEC	breast
32	chr6:141988400-141989800	Enhancers	NHEK	skin
33	chr6:141988400-141990400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:141988600-141989400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:141988600-141989400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:141988600-141990000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:141988600-141990000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:141988800-141989600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:141988800-141989600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:141988800-141989600	Enhancers	Fetal Heart	heart
41	chr6:141988800-141989800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:141988800-141989800	Enhancers	Left Ventricle	heart
43	chr6:141988800-141989800	Enhancers	Right Ventricle	heart
44	chr6:141988800-141990200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr6:141989000-141989400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:141989000-141989800	Enhancers	Placenta Amnion	Placenta Amnion
47	chr6:141989000-141990400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:141989400-141989600	Enhancers	Fetal Muscle Trunk	muscle
49	chr6:141989400-141989800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:141989600-141990400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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