Variant report

Variant	esv3394316
Chromosome Location	chr6:74630005-74935625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1431)
CpG islands
(count:732)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1431 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:74679683-74680028	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:74801147-74801533	HepG2	liver:	n/a	n/a
3	ATF1	chr6:74706732-74706808	K562	blood:	n/a	n/a
4	BACH1	chr6:74760430-74760490	K562	blood:	n/a	n/a
5	BHLHE40	chr6:74760671-74760930	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:74892790-74893173	HepG2	liver:	n/a	n/a
7	BRCA1	chr6:74639173-74639469	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr6:74679648-74680052	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr6:74801110-74801569	HCT-116	colon:	n/a	n/a
10	CBX3	chr6:74847549-74848161	HCT-116	colon:	n/a	n/a
11	CBX3	chr6:74915215-74915733	HCT-116	colon:	n/a	n/a
12	CCNT2	chr6:74827126-74827221	K562	blood:	n/a	n/a
13	CCNT2	chr6:74642357-74642557	K562	blood:	n/a	n/a
14	CEBPB	chr6:74847592-74848136	Hela-S3	cervix:	n/a	chr6:74847919-74847930
15	CEBPB	chr6:74847743-74848092	HepG2	liver:	n/a	chr6:74847919-74847930
16	CEBPB	chr6:74679646-74680059	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:74786155-74786301	HepG2	liver:	n/a	chr6:74786167-74786179 chr6:74786208-74786219 chr6:74786206-74786219 chr6:74786206-74786217
18	CEBPB	chr6:74847773-74848061	A549	lung:	n/a	chr6:74847919-74847930
19	CEBPB	chr6:74825462-74825784	HepG2	liver:	n/a	chr6:74825621-74825632
20	CEBPB	chr6:74785096-74785355	HepG2	liver:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
21	CEBPB	chr6:74833341-74833624	MCF-7	breast:	n/a	chr6:74833523-74833534
22	CEBPB	chr6:74823654-74823896	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:74766470-74766684	HepG2	liver:	n/a	chr6:74766585-74766596
24	CEBPB	chr6:74652311-74652653	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:74923585-74923837	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:74795063-74795245	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:74847635-74848230	HCT-116	colon:	n/a	chr6:74847919-74847930
28	CEBPB	chr6:74847515-74848240	HCT-116	colon:	n/a	chr6:74847919-74847930
29	CEBPB	chr6:74679712-74680117	MCF-7	breast:	n/a	chr6:74680080-74680091 chr6:74680078-74680091
30	CEBPB	chr6:74847710-74848056	ECC-1	luminal epithelium:	n/a	chr6:74847919-74847930
31	CEBPB	chr6:74879906-74880271	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:74779883-74780137	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:74652349-74652709	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr6:74838360-74838570	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:74932618-74932709	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr6:74871166-74871418	HepG2	liver:	n/a	chr6:74871272-74871283
37	CEBPB	chr6:74871207-74871361	K562	blood:	n/a	chr6:74871272-74871283
38	CEBPB	chr6:74871176-74871509	HCT-116	colon:	n/a	chr6:74871272-74871283
39	CEBPB	chr6:74679703-74680003	A549	lung:	n/a	n/a
40	CEBPB	chr6:74811442-74811617	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:74679666-74679938	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr6:74785098-74785334	H1-hESC	embryonic stem cell:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
43	CEBPB	chr6:74871121-74871482	Hela-S3	cervix:	n/a	chr6:74871272-74871283
44	CEBPB	chr6:74679733-74680210	IMR90	lung:	n/a	chr6:74680080-74680091 chr6:74680078-74680091
45	CEBPB	chr6:74652158-74652812	HCT-116	colon:	n/a	n/a
46	CEBPB	chr6:74825498-74825731	H1-hESC	embryonic stem cell:	n/a	chr6:74825621-74825632
47	CEBPB	chr6:74639049-74639599	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:74785083-74785369	IMR90	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122
49	CEBPB	chr6:74633979-74634237	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:74785109-74785309	A549	lung:	n/a	chr6:74785182-74785193 chr6:74785110-74785122

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74647315-74647365	AG04449	skin:	fetal
2	chr6:74801378-74801428	SKMC	muscle:	n/a
3	chr6:74778313-74778363	SK-N-SH_RA	brain:	n/a
4	chr6:74909201-74909251	CMK	blood:	n/a
5	chr6:74784340-74784390	HCF	heart:	n/a
6	chr6:74652865-74652915	Hepatocyte	liver:	n/a
7	chr6:74710701-74710751	Jurkat	blood:	n/a
8	chr6:74784340-74784390	GM12878	blood:	n/a
9	chr6:74700624-74700674	HEEpiC	esophagus:	n/a
10	chr6:74710701-74710751	HEK293	kidney:	embryo
11	chr6:74909201-74909251	HRCEpiC	kidney:	n/a
12	chr6:74909201-74909251	PANC-1	pancreas:	n/a
13	chr6:74877005-74877055	Caco-2	colon:	n/a
14	chr6:74801378-74801428	HAEpiC	amniotic membrane:	n/a
15	chr6:74826447-74826497	NT2-D1	testis:	n/a
16	chr6:74877005-74877055	GM06990	blood:	n/a
17	chr6:74801378-74801428	PFSK-1	brain:	n/a
18	chr6:74778313-74778363	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:74700624-74700674	HAEpiC	amniotic membrane:	n/a
20	chr6:74909201-74909251	HIPEpiC	eye:	n/a
21	chr6:74678454-74678504	HRPEpiC	eye:	n/a
22	chr6:74909201-74909251	AG09309	skin:	n/a
23	chr6:74652865-74652915	SK-N-MC	brain:	n/a
24	chr6:74647315-74647365	HRCEpiC	kidney:	n/a
25	chr6:74784340-74784390	MCF10A-Er-Src	breast:	n/a
26	chr6:74778945-74778995	T-47D	breast:	n/a
27	chr6:74877005-74877055	GM19239	blood:	n/a
28	chr6:74801378-74801428	SAEC	small airway:	n/a
29	chr6:74784340-74784390	HepG2	liver:	n/a
30	chr6:74778313-74778363	PANC-1	pancreas:	n/a
31	chr6:74801378-74801428	Jurkat	blood:	n/a
32	chr6:74784340-74784390	GM19239	blood:	n/a
33	chr6:74909201-74909251	HNPCEpiC	eye:	n/a
34	chr6:74909201-74909251	AG04450	lung:	fetal
35	chr6:74778313-74778363	AG10803	skin:	n/a
36	chr6:74700624-74700674	AG04450	lung:	fetal
37	chr6:74778313-74778363	HCPEpiC	choroid plexus:	n/a
38	chr6:74700624-74700674	HEK293	kidney:	embryo
39	chr6:74700624-74700674	PANC-1	pancreas:	n/a
40	chr6:74778945-74778995	GM19239	blood:	n/a
41	chr6:74784340-74784390	A549	lung:	n/a
42	chr6:74710701-74710751	AG10803	skin:	n/a
43	chr6:74784340-74784390	HIPEpiC	eye:	n/a
44	chr6:74652865-74652915	ovcar-3	ovarian:	n/a
45	chr6:74778945-74778995	PFSK-1	brain:	n/a
46	chr6:74801378-74801428	GM06990	blood:	n/a
47	chr6:74826447-74826497	HCM	heart:	n/a
48	chr6:74652865-74652915	U87	brain:	n/a
49	chr6:74700624-74700674	HCF	heart:	n/a
50	chr6:74784340-74784390	GM12891	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:74892709..74895952-chr6:74900506..74904423,4	K562	blood:
2	chr6:74639600..74641277-chr6:74641826..74644463,2	K562	blood:
3	chr6:74835506..74837786-chr6:74837930..74840707,2	MCF-7	breast:
4	chr6:74676262..74678006-chr6:74678035..74679663,2	MCF-7	breast:
5	chr6:74835506..74837786-chr6:74837930..74840707,2	MCF-7	breast:
6	chr6:74639600..74641277-chr6:74641826..74644463,2	K562	blood:
7	chr6:74724928..74727118-chr6:74734673..74736318,2	MCF-7	breast:
8	chr6:74815697..74817712-chr6:74819517..74822083,2	K562	blood:
9	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:
10	chr6:74870023..74872617-chr6:74890173..74892829,2	MCF-7	breast:
11	chr6:74892709..74895952-chr6:74900506..74904423,4	K562	blood:
12	chr6:74912181..74915078-chr6:74916489..74918406,2	K562	blood:
13	chr6:74812681..74814220-chr6:74816370..74818420,2	K562	blood:
14	chr6:74676262..74678006-chr6:74678035..74679663,2	MCF-7	breast:
15	chr6:74679477..74680332-chr6:75914060..75914724,3	MCF-7	breast:
16	chr6:74564799..74565392-chr6:74801154..74801695,2	MCF-7	breast:
17	chr6:74679584..74680329-chr6:75284218..75285177,4	MCF-7	breast:
18	chr6:74815697..74817712-chr6:74819517..74822083,2	K562	blood:
19	chr6:74564800..74565363-chr6:74797356..74797902,2	MCF-7	breast:
20	chr6:74724928..74727118-chr6:74734673..74736318,2	MCF-7	breast:
21	chr6:74870023..74872617-chr6:74890173..74892829,2	MCF-7	breast:
22	chr6:74912181..74915078-chr6:74916489..74918406,2	K562	blood:
23	chr6:74654318..74655307-chrX:136670826..136671580,2	MCF-7	breast:
24	chr6:74812681..74814220-chr6:74816370..74818420,2	K562	blood:
25	chr6:74564592..74565216-chr6:74679361..74679928,2	MCF-7	breast:
26	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC17A5-2	chr6:74714236-74714528	NONHSAT113584
2	lnc-CD109-8	chr6:74835887-74836024	ucscGeneNc_uc003phr_2
3	lnc-CD109-3	chr6:74779167-74779304	ENSG00000223786.1

No data

Variant related genes	Relation type
ENSG00000223786	TF binding region
TXNP7	TF binding region
ENSG00000223786	CpG island
TXNP7	CpG island

Extended variants
information (count: 4705 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4705 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12210594	chr6:74633611-74633612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547324064	chr6:74633631-74633632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1898484	chr6:74633639-74633640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533005363	chr6:74633643-74633644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12528991	chr6:74633657-74633658	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557901588	chr6:74633666-74633667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575543219	chr6:74633682-74633683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145058869	chr6:74633687-74633688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544938720	chr6:74633692-74633693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534601617	chr6:74633700-74633701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148286537	chr6:74633739-74633740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578237530	chr6:74633767-74633768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189895967	chr6:74633778-74633779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1898485	chr6:74633835-74633836	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1898486	chr6:74633842-74633843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs117278375	chr6:74633849-74633850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1898487	chr6:74633850-74633851	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574920502	chr6:74633859-74633860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374858127	chr6:74633868-74633869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181527196	chr6:74633884-74633885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186401803	chr6:74633892-74633893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201357076	chr6:74633918-74633919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369272801	chr6:74633927-74633928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs58147887	chr6:74633963-74633964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551178852	chr6:74633970-74633971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563365024	chr6:74633981-74633982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372344027	chr6:74634061-74634062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560588670	chr6:74634078-74634079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116889105	chr6:74634088-74634089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548845125	chr6:74634110-74634111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141425391	chr6:74634113-74634114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150895027	chr6:74634133-74634134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534602413	chr6:74634176-74634177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189730178	chr6:74634181-74634182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571983702	chr6:74634189-74634190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539308929	chr6:74634199-74634200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76398325	chr6:74634207-74634208	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs569388158	chr6:74634218-74634219	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs547656613	chr6:74634354-74634355	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs111309767	chr6:74634361-74634362	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs554814716	chr6:74634364-74634365	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs573242371	chr6:74634391-74634392	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs9343088	chr6:74634411-74634412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540242822	chr6:74634420-74634421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373057986	chr6:74634480-74634481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531806711	chr6:74634486-74634487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73449805	chr6:74634517-74634518	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs180893047	chr6:74634537-74634538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544935069	chr6:74634557-74634558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138317605	chr6:74634572-74634573	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	22016467	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74633600-74634200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:74633600-74635000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:74633800-74634200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:74634000-74634400	Enhancers	Colon Smooth Muscle	Colon
5	chr6:74634200-74634400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:74636800-74637000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:74636800-74637000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:74637000-74638800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:74638800-74639400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:74638800-74639800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:74638800-74639800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:74638800-74640000	Enhancers	HMEC	breast
13	chr6:74639000-74639200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:74639000-74639400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr6:74639000-74639800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:74639000-74639800	Enhancers	NHEK	skin
17	chr6:74639000-74640000	Enhancers	Hela-S3	cervix
18	chr6:74639200-74639600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:74642200-74643000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr6:74642400-74643000	Enhancers	Fetal Brain Female	brain
21	chr6:74642600-74643200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:74642800-74643200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:74642800-74643200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:74642800-74643200	Enhancers	Colon Smooth Muscle	Colon
25	chr6:74642800-74643200	Enhancers	Fetal Brain Male	brain
26	chr6:74642800-74643200	Enhancers	Fetal Muscle Leg	muscle
27	chr6:74642800-74643200	Enhancers	Rectal Smooth Muscle	rectum
28	chr6:74643200-74647200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:74647200-74647400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:74647400-74648000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:74648000-74648200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:74652000-74653400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:74652000-74653600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:74652000-74654800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:74652200-74653400	Enhancers	NHLF	lung
36	chr6:74652200-74653800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:74652400-74653000	Enhancers	HMEC	breast
38	chr6:74652400-74654200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr6:74652400-74654200	Enhancers	NHDF-Ad	bronchial
40	chr6:74653200-74653400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:74653600-74654000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:74657600-74658200	ZNF genes & repeats	Spleen	Spleen
43	chr6:74657600-74658400	ZNF genes & repeats	Pancreas	Pancrea
44	chr6:74658200-74658400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:74658200-74660600	Weak transcription	Spleen	Spleen
46	chr6:74660600-74660800	Enhancers	Spleen	Spleen
47	chr6:74660600-74661000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:74660600-74661600	Enhancers	NHDF-Ad	bronchial
49	chr6:74660600-74661800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:74660800-74661600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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