Variant report

Variant	esv1841066
Chromosome Location	chr3:61534766-61550452
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	ARID3A	chr3:61546348-61547410	HepG2	liver:	n/a	n/a
2	ATF2	chr3:61546768-61547241	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:61550039-61550697	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:61546127-61546816	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:61546913-61546993	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:61549892-61550733	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:61546097-61546615	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr3:61547632-61547639	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:61550308-61550544	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:61546189-61546457	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:61546738-61547318	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:61548846-61548873	GM12878	blood:	n/a	n/a
13	BRCA1	chr3:61547062-61547312	HepG2	liver:	n/a	n/a
14	BRCA1	chr3:61546481-61546734	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr3:61550375-61550474	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr3:61545545-61545576	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:61546154-61546860	ECC-1	luminal epithelium:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
18	CEBPB	chr3:61546007-61547518	HCT-116	colon:	n/a	chr3:61546132-61546143 chr3:61546567-61546576 chr3:61546132-61546143 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
19	CEBPB	chr3:61550157-61550557	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:61546190-61547179	ECC-1	luminal epithelium:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
21	CEBPB	chr3:61546258-61546839	MCF-7	breast:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
22	CEBPB	chr3:61546198-61546825	HepG2	liver:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
23	CEBPB	chr3:61546178-61546788	HepG2	liver:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
24	CEBPB	chr3:61546170-61546878	HepG2	liver:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
25	CEBPB	chr3:61546264-61546776	A549	lung:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
26	CEBPB	chr3:61546168-61546882	IMR90	lung:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
27	CEBPB	chr3:61546164-61547245	H1-hESC	embryonic stem cell:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
28	CEBPB	chr3:61546277-61546711	HepG2	liver:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
29	CEBPB	chr3:61546222-61546801	MCF-7	breast:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
30	CEBPB	chr3:61545284-61545503	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:61546270-61546755	A549	lung:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
32	CEBPB	chr3:61546159-61546826	A549	lung:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
33	CEBPB	chr3:61545993-61546957	HCT-116	colon:	n/a	chr3:61546132-61546143 chr3:61546567-61546576 chr3:61546132-61546143 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
34	CEBPB	chr3:61546378-61546759	K562	blood:	n/a	chr3:61546567-61546576 chr3:61546565-61546576 chr3:61546567-61546576 chr3:61546567-61546576
35	CEBPD	chr3:61546294-61546882	HepG2	liver:	n/a	chr3:61546567-61546576
36	CEBPD	chr3:61546972-61547424	HepG2	liver:	n/a	n/a
37	CEBPD	chr3:61546483-61546729	HepG2	liver:	n/a	chr3:61546567-61546576
38	CHD1	chr3:61545613-61550962	IMR90	lung:	n/a	chr3:61550522-61550532
39	CHD1	chr3:61546237-61546894	GM12878	blood:	n/a	n/a
40	CHD1	chr3:61546000-61548206	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr3:61548445-61549415	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr3:61548503-61549006	HepG2	liver:	n/a	n/a
43	CHD2	chr3:61545095-61545392	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr3:61548674-61548809	GM12878	blood:	n/a	n/a
45	CHD2	chr3:61546078-61547299	GM12878	blood:	n/a	n/a
46	CHD2	chr3:61546341-61547417	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr3:61550169-61550581	H1-hESC	embryonic stem cell:	n/a	chr3:61550522-61550532
48	CHD2	chr3:61546327-61547452	HepG2	liver:	n/a	n/a
49	CHD2	chr3:61550071-61550600	GM12878	blood:	n/a	chr3:61550522-61550532
50	CREB1	chr3:61550142-61550726	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:61547524-61547574	CMK	blood:	n/a
2	chr3:61547211-61547261	SAEC	small airway:	n/a
3	chr3:61547524-61547574	CMK	blood:	n/a
4	chr3:61547211-61547261	SAEC	small airway:	n/a
5	chr3:61547285-61547335	GM12878	blood:	n/a
6	chr3:61546343-61546393	Caco-2	colon:	n/a
7	chr3:61547211-61547261	AG04450	lung:	fetal
8	chr3:61546472-61546522	PFSK-1	brain:	n/a
9	chr3:61546343-61546393	HMEC	breast:	n/a
10	chr3:61546275-61546325	ovcar-3	ovarian:	n/a
11	chr3:61548172-61548222	HRE	kidney:	n/a
12	chr3:61548172-61548222	AG04449	skin:	fetal
13	chr3:61547285-61547335	PANC-1	pancreas:	n/a
14	chr3:61548172-61548222	PrEC	prostate:	n/a
15	chr3:61546275-61546325	AG09319	gingival:	n/a
16	chr3:61547944-61547994	BE2_C	brain:	n/a
17	chr3:61546343-61546393	HAEpiC	amniotic membrane:	n/a
18	chr3:61550379-61550429	ovcar-3	ovarian:	n/a
19	chr3:61549475-61549525	AG10803	skin:	n/a
20	chr3:61547130-61547180	NHDF-neo	bronchial:	n/a
21	chr3:61547196-61547246	MCF10A-Er-Src	breast:	n/a
22	chr3:61549475-61549525	HNPCEpiC	eye:	n/a
23	chr3:61547104-61547154	AG09319	gingival:	n/a
24	chr3:61546275-61546325	K562	blood:	n/a
25	chr3:61547208-61547258	ECC-1	luminal epithelium:	n/a
26	chr3:61547211-61547261	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:61547130-61547180	GM12892	blood:	n/a
28	chr3:61546275-61546325	BJ	skin:	n/a
29	chr3:61547287-61547337	HIPEpiC	eye:	n/a
30	chr3:61546343-61546393	HUVEC	blood vessel:	n/a
31	chr3:61543023-61543073	HCM	heart:	n/a
32	chr3:61547104-61547154	PFSK-1	brain:	n/a
33	chr3:61546526-61546576	LNCaP	prostate:	n/a
34	chr3:61547524-61547574	RPTEC	kidney:	n/a
35	chr3:61547285-61547335	IMR90	lung:	fetal
36	chr3:61546275-61546325	HCM	heart:	n/a
37	chr3:61547211-61547261	AG09309	skin:	n/a
38	chr3:61547211-61547261	HEEpiC	esophagus:	n/a
39	chr3:61547208-61547258	Hela-S3	cervix:	n/a
40	chr3:61543023-61543073	NB4	blood:	n/a
41	chr3:61547287-61547337	PrEC	prostate:	n/a
42	chr3:61548332-61548382	SK-N-MC	brain:	n/a
43	chr3:61543023-61543073	ovcar-3	ovarian:	n/a
44	chr3:61548172-61548222	GM12891	blood:	n/a
45	chr3:61548332-61548382	HL-60	blood:	n/a
46	chr3:61547524-61547574	HepG2	liver:	n/a
47	chr3:61546526-61546576	HCF	heart:	n/a
48	chr3:61548172-61548222	ProgFib	skin:	n/a
49	chr3:61547287-61547337	BE2_C	brain:	n/a
50	chr3:61547944-61547994	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:61541363..61545409-chr3:61545583..61548750,5	MCF-7	breast:
2	chr3:61543024..61544973-chr3:61553525..61555086,2	MCF-7	breast:
3	chr3:61547884..61549685-chr3:61773585..61775750,2	MCF-7	breast:
4	chr3:61538544..61540472-chr3:61544545..61547220,2	K562	blood:
5	chr3:61538544..61540472-chr3:61544545..61547220,2	K562	blood:
6	chr1:234744695..234746368-chr3:61546699..61548508,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRG-2	chr3:61547525-61548046	NONHSAT090170

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTPRG	hsa-miR-193b-3p	chr3:61547255-61547276

Variant related genes	Relation type
PTPRG	TF binding region
PTPRG	CpG island
ENSG00000144724	chromatin interactions
ENSG00000168264	chromatin interactions

Extended variants
information (count: 676 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386661565	chr3:61534766-61534767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7649299	chr3:61534768-61534769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs369427025	chr3:61534798-61534799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187153907	chr3:61534839-61534840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539241503	chr3:61534863-61534864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571885491	chr3:61534901-61534902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548553093	chr3:61534921-61534922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561213658	chr3:61534922-61534923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7627324	chr3:61534969-61534970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs375011640	chr3:61534977-61534978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369442972	chr3:61534982-61534983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372064219	chr3:61535008-61535009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376885870	chr3:61535009-61535010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534104706	chr3:61535063-61535064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376351012	chr3:61535090-61535091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9809796	chr3:61535172-61535173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13059759	chr3:61535178-61535179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs375389341	chr3:61535180-61535181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142510632	chr3:61535191-61535192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374429192	chr3:61535196-61535197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200407627	chr3:61535219-61535220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9865034	chr3:61535230-61535231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs377657256	chr3:61535238-61535239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13080061	chr3:61535239-61535240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573231252	chr3:61535269-61535270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62243005	chr3:61535275-61535276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146822067	chr3:61535307-61535308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576507757	chr3:61535331-61535332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370708142	chr3:61535332-61535333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544746312	chr3:61535359-61535360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9865322	chr3:61535367-61535368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs574872679	chr3:61535396-61535397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190449552	chr3:61535413-61535414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372817466	chr3:61535453-61535454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527649685	chr3:61535457-61535458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555356048	chr3:61535458-61535459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181383371	chr3:61535485-61535486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141869334	chr3:61535498-61535499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185490241	chr3:61535501-61535502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550743532	chr3:61535592-61535593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568908486	chr3:61535635-61535636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116247578	chr3:61535655-61535656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190007894	chr3:61535656-61535657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547870206	chr3:61535671-61535672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540928089	chr3:61535687-61535688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533516897	chr3:61535696-61535697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58583962	chr3:61535700-61535701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558828925	chr3:61535708-61535709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59008966	chr3:61535729-61535730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113441253	chr3:61535731-61535732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:61523200-61545000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:61538200-61538600	Enhancers	Liver	Liver
3	chr3:61542000-61542200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:61542200-61545600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:61543800-61545400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:61544600-61545000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:61544600-61545400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:61544800-61545000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr3:61544800-61545200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr3:61544800-61545200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr3:61544800-61545200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:61544800-61545400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:61544800-61545400	Enhancers	Placenta	Placenta
14	chr3:61545000-61545200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:61545000-61545200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:61545000-61545200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:61545000-61545200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:61545000-61545200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
19	chr3:61545000-61545200	Enhancers	Right Atrium	heart
20	chr3:61545000-61545200	Enhancers	Right Ventricle	heart
21	chr3:61545000-61545200	Enhancers	HepG2	liver
22	chr3:61545000-61545400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:61545000-61545400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr3:61545000-61545400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:61545000-61545400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr3:61545000-61545400	Enhancers	Left Ventricle	heart
27	chr3:61545000-61545400	Enhancers	HUVEC	blood vessel
28	chr3:61545000-61545400	Enhancers	NHLF	lung
29	chr3:61545000-61545600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr3:61545000-61545600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr3:61545000-61545600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:61545000-61545600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr3:61545000-61545600	Enhancers	Fetal Kidney	kidney
34	chr3:61545000-61545600	Enhancers	Fetal Muscle Leg	muscle
35	chr3:61545000-61545600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr3:61545000-61545600	Enhancers	NHDF-Ad	bronchial
37	chr3:61545000-61545800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr3:61545000-61545800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:61545000-61545800	Flanking Active TSS	Osteobl	bone
40	chr3:61545000-61546000	Enhancers	Fetal Heart	heart
41	chr3:61545000-61547800	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr3:61545000-61549600	Active TSS	NHEK	skin
43	chr3:61545000-61550800	Active TSS	Psoas Muscle	Psoas
44	chr3:61545200-61545400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr3:61545200-61545400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
46	chr3:61545200-61545400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr3:61545200-61545400	Enhancers	Adipose Nuclei	Adipose
48	chr3:61545200-61545400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr3:61545200-61545600	Flanking Active TSS	H9 Cell Line	embryonic stem cell
50	chr3:61545200-61545600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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