Variant report

Variant	nsv877114
Chromosome Location	chr3:86257272-86328961
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	chr3:86318438-86319020	HepG2	liver:	n/a	n/a
2	BATF	chr3:86307090-86307397	GM12878	blood:	n/a	n/a
3	BATF	chr3:86307118-86307476	GM12878	blood:	n/a	n/a
4	BCL3	chr3:86274515-86275085	A549	lung:	n/a	n/a
5	BCL3	chr3:86278153-86278659	A549	lung:	n/a	n/a
6	BCL3	chr3:86278075-86278666	A549	lung:	n/a	n/a
7	BHLHE40	chr3:86318567-86318905	HepG2	liver:	n/a	n/a
8	BRCA1	chr3:86318516-86318663	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr3:86287187-86287218	GM12878	blood:	n/a	n/a
10	CCNT2	chr3:86288357-86288546	K562	blood:	n/a	n/a
11	CEBPB	chr3:86315916-86316138	K562	blood:	n/a	chr3:86316026-86316037
12	CEBPB	chr3:86278176-86278631	A549	lung:	n/a	n/a
13	CEBPB	chr3:86321870-86322089	A549	lung:	n/a	chr3:86321975-86321986
14	CEBPB	chr3:86274618-86274952	A549	lung:	n/a	n/a
15	CEBPB	chr3:86283189-86283402	A549	lung:	n/a	n/a
16	CEBPB	chr3:86278150-86278633	A549	lung:	n/a	n/a
17	CEBPB	chr3:86274554-86275097	A549	lung:	n/a	n/a
18	CEBPB	chr3:86315901-86316202	HepG2	liver:	n/a	chr3:86316026-86316037
19	CEBPB	chr3:86315904-86316209	A549	lung:	n/a	chr3:86316026-86316037
20	CEBPB	chr3:86277988-86278695	A549	lung:	n/a	n/a
21	CEBPB	chr3:86265838-86266154	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:86315871-86316212	IMR90	lung:	n/a	chr3:86316026-86316037
23	CEBPB	chr3:86318491-86318829	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:86321834-86322156	HepG2	liver:	n/a	chr3:86321975-86321986
25	CEBPB	chr3:86275166-86275602	A549	lung:	n/a	n/a
26	CEBPB	chr3:86275173-86275480	A549	lung:	n/a	n/a
27	CREB1	chr3:86318407-86318961	HepG2	liver:	n/a	n/a
28	CTCF	chr3:86294579-86294903	GM12878	blood:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
29	CTCF	chr3:86294580-86294730	HEK293	kidney:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
30	CTCF	chr3:86294494-86294903	MCF-7	breast:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
31	CTCF	chr3:86294600-86294750	WERI-Rb-1	eye:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
32	CTCF	chr3:86294660-86294810	HPF	lung:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
33	CTCF	chr3:86294580-86294730	SAEC	small airway:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
34	CTCF	chr3:86294613-86294829	LNCaP	prostate:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
35	CTCF	chr3:86294607-86294821	LNCaP	prostate:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
36	CTCF	chr3:86294612-86294811	Hela-S3	cervix:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
37	CTCF	chr3:86294640-86294790	HepG2	liver:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
38	CTCF	chr3:86294687-86294771	GM13977	blood:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
39	CTCF	chr3:86294690-86294773	GM12878	blood:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
40	CTCF	chr3:86294620-86294770	HRPEpiC	eye:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
41	CTCF	chr3:86294635-86294805	Pancreas_OC	pancreas:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
42	CTCF	chr3:86305640-86305790	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr3:86294481-86294850	H1-hESC	embryonic stem cell:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
44	CTCF	chr3:86294460-86294610	A549	lung:	n/a	n/a
45	CTCF	chr3:86294660-86294810	Caco-2	colon:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
46	CTCF	chr3:86294660-86294810	HBMEC	blood vessel:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
47	CTCF	chr3:86294640-86294790	HEEpiC	esophagus:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
48	CTCF	chr3:86294599-86294821	Medullo	brain:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
49	CTCF	chr3:86294640-86294790	SK-N-SH_RA	brain:	n/a	chr3:86294711-86294719 chr3:86294699-86294720
50	CTCF	chr3:86294528-86294851	A549	lung:	n/a	chr3:86294711-86294719 chr3:86294699-86294720

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:86277500-86277550	NB4	blood:	n/a
2	chr3:86277500-86277550	HRPEpiC	eye:	n/a
3	chr3:86277500-86277550	HCM	heart:	n/a
4	chr3:86277500-86277550	HMEC	breast:	n/a
5	chr3:86277500-86277550	K562	blood:	n/a
6	chr3:86277500-86277550	CMK	blood:	n/a
7	chr3:86277500-86277550	H1-hESC	embryonic stem cell:	embryo
8	chr3:86277500-86277550	AG09319	gingival:	n/a
9	chr3:86277500-86277550	GM06990	blood:	n/a
10	chr3:86277500-86277550	AG04449	skin:	fetal
11	chr3:86277500-86277550	MCF-7	breast:	n/a
12	chr3:86277500-86277550	HL-60	blood:	n/a
13	chr3:86277500-86277550	HIPEpiC	eye:	n/a
14	chr3:86277500-86277550	BJ	skin:	n/a
15	chr3:86277500-86277550	HepG2	liver:	n/a
16	chr3:86277500-86277550	NH-A	brain:	n/a
17	chr3:86277500-86277550	GM12892	blood:	n/a
18	chr3:86277500-86277550	U87	brain:	n/a
19	chr3:86277500-86277550	GM19239	blood:	n/a
20	chr3:86277500-86277550	NT2-D1	testis:	n/a
21	chr3:86277500-86277550	HRE	kidney:	n/a
22	chr3:86277500-86277550	T-47D	breast:	n/a
23	chr3:86277500-86277550	HCPEpiC	choroid plexus:	n/a
24	chr3:86277500-86277550	A549	lung:	n/a
25	chr3:86277500-86277550	HCF	heart:	n/a
26	chr3:86277500-86277550	HCT-116	colon:	n/a
27	chr3:86277500-86277550	Jurkat	blood:	n/a
28	chr3:86277500-86277550	NHDF-neo	bronchial:	n/a
29	chr3:86277500-86277550	SK-N-SH	brain:	n/a
30	chr3:86277500-86277550	ECC-1	luminal epithelium:	n/a
31	chr3:86277500-86277550	SK-N-MC	brain:	n/a
32	chr3:86277500-86277550	HRCEpiC	kidney:	n/a
33	chr3:86277500-86277550	LNCaP	prostate:	n/a
34	chr3:86277500-86277550	Caco-2	colon:	n/a
35	chr3:86277500-86277550	BE2_C	brain:	n/a
36	chr3:86277500-86277550	HEEpiC	esophagus:	n/a
37	chr3:86277500-86277550	HEK293	kidney:	embryo
38	chr3:86277500-86277550	SAEC	small airway:	n/a
39	chr3:86277500-86277550	HUVEC	blood vessel:	n/a
40	chr3:86277500-86277550	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:86277500-86277550	AG09309	skin:	n/a
42	chr3:86277500-86277550	PrEC	prostate:	n/a
43	chr3:86277500-86277550	HNPCEpiC	eye:	n/a
44	chr3:86277500-86277550	IMR90	lung:	fetal
45	chr3:86277500-86277550	Hela-S3	cervix:	n/a
46	chr3:86277500-86277550	NHBE	bronchial:	n/a
47	chr3:86277500-86277550	AG10803	skin:	n/a
48	chr3:86277500-86277550	SKMC	muscle:	n/a
49	chr3:86277500-86277550	ProgFib	skin:	n/a
50	chr3:86277500-86277550	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:86301755..86304076-chr3:86304582..86306274,2	MCF-7	breast:
2	chr3:86301755..86304076-chr3:86304582..86306274,2	MCF-7	breast:
3	chr3:85870003..85870955-chr3:86294230..86295150,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VGLL3-2	chr3:86316405-86316546	NONHSAT090669
2	lnc-VGLL3-2	chr3:86313728-86314043	NONHSAT090669
3	lnc-VGLL3-3	chr3:86271854-86271969	XLOC_003175
4	lnc-VGLL3-2	chr3:86313729-86314043	XLOC_003176
5	lnc-VGLL3-2	chr3:86313705-86314043	XLOC_003176
6	lnc-VGLL3-2	chr3:86316406-86316546	XLOC_003176
7	lnc-VGLL3-2	chr3:86316146-86316511	XLOC_003176

Variant related genes	Relation type
RNU6-1129P	TF binding region
ENSG00000239767	TF binding region
RNU6-1129P	CpG island
ENSG00000239767	CpG island
AGFG1	miRNA target sites

Extended variants
information (count: 1125 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs883776	chr3:86257272-86257273	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370059766	chr3:86257306-86257307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548140174	chr3:86257324-86257325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566488675	chr3:86257326-86257327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189891368	chr3:86257329-86257330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560916447	chr3:86257369-86257370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529701550	chr3:86257421-86257422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201850078	chr3:86257496-86257497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374343413	chr3:86257505-86257506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574743883	chr3:86257519-86257520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552901489	chr3:86257554-86257555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571203935	chr3:86257555-86257556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538419331	chr3:86257614-86257615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182111289	chr3:86257615-86257616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187259177	chr3:86257619-86257620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535594078	chr3:86257681-86257682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192585213	chr3:86257687-86257688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554333693	chr3:86257692-86257693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367562703	chr3:86257709-86257710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572108535	chr3:86257725-86257726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183803191	chr3:86257786-86257787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73132566	chr3:86257795-86257796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576759543	chr3:86257834-86257835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546254961	chr3:86257842-86257843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376862704	chr3:86257866-86257867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544372388	chr3:86257870-86257871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562561576	chr3:86257920-86257921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371469887	chr3:86257923-86257924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34647097	chr3:86257935-86257936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77168600	chr3:86257937-86257938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571741557	chr3:86257965-86257966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35712568	chr3:86257979-86257980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115849864	chr3:86258020-86258021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576623579	chr3:86258029-86258030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542213830	chr3:86258093-86258094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560337369	chr3:86258147-86258148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532125827	chr3:86258176-86258177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551972082	chr3:86258178-86258179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193300751	chr3:86258208-86258209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562077035	chr3:86258209-86258210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368567259	chr3:86258244-86258245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372331095	chr3:86258247-86258248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368239141	chr3:86258248-86258249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531935224	chr3:86258391-86258392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550316811	chr3:86258423-86258424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142783812	chr3:86258427-86258428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568572922	chr3:86258466-86258467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372515700	chr3:86258489-86258490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565800173	chr3:86258517-86258518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148491778	chr3:86258553-86258554	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86256800-86258800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:86257000-86258400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:86257200-86257600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:86257200-86258200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:86257200-86258600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:86257200-86259000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:86257400-86258400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:86257400-86258400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:86272800-86273000	Enhancers	A549	lung
10	chr3:86273000-86273600	Weak transcription	A549	lung
11	chr3:86273600-86274400	Enhancers	A549	lung
12	chr3:86274400-86274800	Flanking Active TSS	A549	lung
13	chr3:86274800-86278000	Weak transcription	A549	lung
14	chr3:86276800-86277000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:86277000-86277400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:86277400-86277800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:86277800-86284200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:86278000-86278200	Flanking Active TSS	A549	lung
19	chr3:86278200-86279000	Active TSS	A549	lung
20	chr3:86283800-86284200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr3:86283800-86285000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:86283800-86287000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:86283800-86287000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr3:86284000-86284200	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:86284200-86284600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:86284200-86286600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:86284400-86285400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr3:86284400-86285600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr3:86284600-86284800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:86284600-86285000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:86284600-86286000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:86284800-86285800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:86285000-86285200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:86285000-86285400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr3:86285000-86285800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:86285200-86286200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr3:86285400-86287000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr3:86285400-86289000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr3:86285600-86286600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr3:86285800-86286600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:86286200-86286600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr3:86286200-86286600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:86286400-86287000	Enhancers	Fetal Heart	heart
44	chr3:86286600-86286800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:86286600-86286800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:86286600-86287800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr3:86286600-86288800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr3:86286800-86288600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:86287000-86289000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr3:86287000-86289200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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