Variant report

Variant	nsv1008766
Chromosome Location	chr1:187412042-187467969
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	chr1:187460152-187460921	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:187412461-187412474	GM12878	blood:	n/a	n/a
3	CEBPB	chr1:187422546-187422771	HepG2	liver:	n/a	chr1:187422633-187422644
4	CEBPB	chr1:187448514-187448722	HepG2	liver:	n/a	chr1:187448620-187448631
5	CEBPB	chr1:187460475-187460902	MCF-7	breast:	n/a	n/a
6	CEBPB	chr1:187460064-187461119	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:187422597-187422795	A549	lung:	n/a	chr1:187422633-187422644
8	CEBPB	chr1:187423188-187423501	HepG2	liver:	n/a	chr1:187423353-187423366 chr1:187423316-187423327 chr1:187423353-187423364 chr1:187423317-187423326
9	CEBPB	chr1:187440728-187441089	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:187425468-187425769	HepG2	liver:	n/a	chr1:187425596-187425607 chr1:187425672-187425685 chr1:187425666-187425677
11	CEBPB	chr1:187448517-187448764	IMR90	lung:	n/a	chr1:187448620-187448631
12	CEBPB	chr1:187442220-187442519	IMR90	lung:	n/a	chr1:187442364-187442375
13	CEBPB	chr1:187425556-187425620	K562	blood:	n/a	chr1:187425596-187425607
14	CEBPB	chr1:187439056-187439256	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:187442223-187442535	HepG2	liver:	n/a	chr1:187442364-187442375
16	CEBPB	chr1:187460418-187461002	MCF-7	breast:	n/a	n/a
17	CEBPB	chr1:187460607-187460877	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:187442226-187442532	A549	lung:	n/a	chr1:187442364-187442375
19	CEBPB	chr1:187460304-187460894	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:187439144-187439172	K562	blood:	n/a	n/a
21	CEBPB	chr1:187423214-187423462	IMR90	lung:	n/a	chr1:187423353-187423366 chr1:187423316-187423327 chr1:187423353-187423364 chr1:187423317-187423326
22	CTCF	chr1:187445900-187446050	HCM	heart:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
23	CTCF	chr1:187445780-187446010	Hela-S3	cervix:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
24	CTCF	chr1:187445960-187446110	HBMEC	blood vessel:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
25	CTCF	chr1:187446292-187446334	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr1:187445860-187446010	NB4	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
27	CTCF	chr1:187445860-187446010	GM12865	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
28	CTCF	chr1:187445920-187446070	Caco-2	colon:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
29	CTCF	chr1:187445839-187446097	Medullo	brain:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
30	CTCF	chr1:187445900-187446050	SAEC	small airway:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
31	CTCF	chr1:187440097-187440134	GM10248	blood:	n/a	n/a
32	CTCF	chr1:187445906-187446003	GM12878	blood:	n/a	chr1:187445982-187446000
33	CTCF	chr1:187445800-187445950	A549	lung:	n/a	n/a
34	CTCF	chr1:187445897-187446042	LNCaP	prostate:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
35	CTCF	chr1:187417730-187417758	GM13976	blood:	n/a	n/a
36	CTCF	chr1:187445900-187446050	HCPEpiC	choroid plexus:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
37	CTCF	chr1:187445880-187446030	GM12875	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
38	CTCF	chr1:187445791-187446173	IMR90	lung:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
39	CTCF	chr1:187445940-187446090	HCFaa	heart:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
40	CTCF	chr1:187445742-187446256	MCF-7	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
41	CTCF	chr1:187445940-187446090	Caco-2	colon:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
42	CTCF	chr1:187445920-187446070	HUVEC	blood vessel:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
43	CTCF	chr1:187445952-187446037	Pancreas_OC	pancreas:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
44	CTCF	chr1:187445920-187446070	RPTEC	kidney:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
45	CTCF	chr1:187445880-187446030	GM12873	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
46	CTCF	chr1:187445940-187446090	MCF-7	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
47	CTCF	chr1:187445880-187446020	MCF-7	breast:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
48	CTCF	chr1:187445845-187446156	K562	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
49	CTCF	chr1:187445860-187446010	GM12872	blood:	n/a	chr1:187445982-187446000 chr1:187445984-187446005
50	CTCF	chr1:187445880-187446030	HA-sp	spinal cord:	n/a	chr1:187445982-187446000 chr1:187445984-187446005

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:187445635-187445685	ovcar-3	ovarian:	n/a
2	chr1:187445635-187445685	ovcar-3	ovarian:	n/a
3	chr1:187460781-187460831	HCPEpiC	choroid plexus:	n/a
4	chr1:187460781-187460831	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:187460781-187460831	GM19239	blood:	n/a
6	chr1:187445635-187445685	PANC-1	pancreas:	n/a
7	chr1:187460781-187460831	AG04450	lung:	fetal
8	chr1:187460781-187460831	HNPCEpiC	eye:	n/a
9	chr1:187445635-187445685	HCM	heart:	n/a
10	chr1:187445635-187445685	AG10803	skin:	n/a
11	chr1:187445635-187445685	H1-hESC	embryonic stem cell:	embryo
12	chr1:187445635-187445685	PFSK-1	brain:	n/a
13	chr1:187460781-187460831	PrEC	prostate:	n/a
14	chr1:187445635-187445685	Jurkat	blood:	n/a
15	chr1:187445635-187445685	HUVEC	blood vessel:	n/a
16	chr1:187460781-187460831	GM06990	blood:	n/a
17	chr1:187445635-187445685	AG04449	skin:	fetal
18	chr1:187445635-187445685	HepG2	liver:	n/a
19	chr1:187445635-187445685	MCF10A-Er-Src	breast:	n/a
20	chr1:187445635-187445685	SK-N-MC	brain:	n/a
21	chr1:187445635-187445685	AoSMC	blood vessel:	n/a
22	chr1:187460781-187460831	AG04449	skin:	fetal
23	chr1:187460781-187460831	HAEpiC	amniotic membrane:	n/a
24	chr1:187460781-187460831	HepG2	liver:	n/a
25	chr1:187460781-187460831	AG09319	gingival:	n/a
26	chr1:187445635-187445685	HL-60	blood:	n/a
27	chr1:187460781-187460831	A549	lung:	n/a
28	chr1:187460781-187460831	Hepatocyte	liver:	n/a
29	chr1:187460781-187460831	HRCEpiC	kidney:	n/a
30	chr1:187460781-187460831	HRPEpiC	eye:	n/a
31	chr1:187445635-187445685	GM12891	blood:	n/a
32	chr1:187445635-187445685	ProgFib	skin:	n/a
33	chr1:187460781-187460831	BE2_C	brain:	n/a
34	chr1:187445635-187445685	HRE	kidney:	n/a
35	chr1:187445635-187445685	HCF	heart:	n/a
36	chr1:187445635-187445685	NB4	blood:	n/a
37	chr1:187460781-187460831	GM12891	blood:	n/a
38	chr1:187445635-187445685	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:187460781-187460831	HRE	kidney:	n/a
40	chr1:187460781-187460831	MCF10A-Er-Src	breast:	n/a
41	chr1:187460781-187460831	HCT-116	colon:	n/a
42	chr1:187460781-187460831	NT2-D1	testis:	n/a
43	chr1:187460781-187460831	AoSMC	blood vessel:	n/a
44	chr1:187445635-187445685	GM06990	blood:	n/a
45	chr1:187460781-187460831	T-47D	breast:	n/a
46	chr1:187460781-187460831	PANC-1	pancreas:	n/a
47	chr1:187460781-187460831	H1-hESC	embryonic stem cell:	embryo
48	chr1:187445635-187445685	HRPEpiC	eye:	n/a
49	chr1:187460781-187460831	CMK	blood:	n/a
50	chr1:187445635-187445685	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:187416875..187419307-chr1:187424025..187426500,2	K562	blood:
2	chr1:187414230..187415836-chr1:187419898..187422220,2	MCF-7	breast:
3	chr1:187445440..187446428-chr1:187968865..187969402,5	MCF-7	breast:
4	chr1:187414230..187415836-chr1:187419898..187422220,2	MCF-7	breast:
5	chr1:187449317..187451017-chr1:187452914..187454633,2	MCF-7	breast:
6	chr1:187435652..187437639-chr1:187437759..187439886,2	MCF-7	breast:
7	chr1:187445527..187446417-chr1:187482131..187482720,2	MCF-7	breast:
8	chr1:187234168..187234815-chr1:187445615..187446278,2	MCF-7	breast:
9	chr1:187435652..187437639-chr1:187437759..187439886,2	MCF-7	breast:
10	chr1:187432536..187433097-chr2:76517809..76518771,2	MCF-7	breast:
11	chr1:187416875..187419307-chr1:187424025..187426500,2	K562	blood:
12	chr1:187460603..187462421-chr1:187469087..187470836,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-2	chr1:187439203-187439371	XLOC_000498
2	lnc-PLA2G4A-2	chr1:187439203-187439324	XLOC_000498
3	lnc-PLA2G4A-2	chr1:187412760-187412858	XLOC_000498
4	lnc-PLA2G4A-2	chr1:187446152-187446354	XLOC_000498
5	lnc-PLA2G4A-2	chr1:187439174-187439394	NONHSAT008463
6	lnc-PLA2G4A-2	chr1:187449425-187449746	ENSG00000272827.1
7	lnc-PLA2G4A-2	chr1:187443288-187449968	NONHSAT008463
8	lnc-PLA2G4A-2	chr1:187412738-187412858	XLOC_000498

Variant related genes	Relation type
LINC01037	TF binding region
ENSG00000272827	TF binding region
LINC01037	CpG island
ENSG00000272827	CpG island
ENSG00000272827	chromatin interactions
MINPP1	miRNA target sites
LRPPRC	miRNA target sites
TMEM138	miRNA target sites

Extended variants
information (count: 1551 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1551 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2244067	chr1:187412042-187412043	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	disease
2	rs185022372	chr1:187412099-187412100	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576357227	chr1:187412128-187412129	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs190999919	chr1:187412153-187412154	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs72641771	chr1:187412229-187412230	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573529004	chr1:187412237-187412238	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs534765969	chr1:187412246-187412247	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs183230686	chr1:187412324-187412325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554813123	chr1:187412352-187412353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559064099	chr1:187412369-187412370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532875277	chr1:187412373-187412374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188542364	chr1:187412389-187412390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563161898	chr1:187412430-187412431	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs367770489	chr1:187412439-187412440	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200628254	chr1:187412450-187412451	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs12081330	chr1:187412469-187412470	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191910266	chr1:187412505-187412506	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568730907	chr1:187412582-187412583	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs183235470	chr1:187412590-187412591	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs371427086	chr1:187412605-187412606	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs75731751	chr1:187412617-187412618	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548018318	chr1:187412642-187412643	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs576371511	chr1:187412652-187412653	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368169972	chr1:187412658-187412659	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs552259323	chr1:187412682-187412683	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs371864563	chr1:187412685-187412686	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs202206414	chr1:187412748-187412749	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs545089433	chr1:187412760-187412761	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs539961222	chr1:187412812-187412813	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs188349099	chr1:187412837-187412838	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs191662230	chr1:187412877-187412878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12062069	chr1:187412956-187412957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138214782	chr1:187412960-187412961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573591115	chr1:187412968-187412969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540889121	chr1:187412979-187412980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74135612	chr1:187412995-187412996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148519194	chr1:187413042-187413043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7418131	chr1:187413059-187413060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375311809	chr1:187413060-187413061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201253270	chr1:187413061-187413062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544795270	chr1:187413065-187413066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76931175	chr1:187413072-187413073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs397773011	chr1:187413073-187413074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553865743	chr1:187413074-187413075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530468816	chr1:187413080-187413081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542596949	chr1:187413096-187413097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116579642	chr1:187413097-187413098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2243884	chr1:187413105-187413106	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs183911659	chr1:187413124-187413125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369798103	chr1:187413202-187413203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:187411400-187412800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:187411600-187413400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:187411800-187412600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr1:187412000-187413400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:187413000-187413200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr1:187413000-187413400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:187413200-187413800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:187413800-187414600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:187414000-187415000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:187415000-187421600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:187421000-187421400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:187421400-187422200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:187421600-187422000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr1:187421600-187422000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:187422200-187423200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:187429000-187430000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:187429200-187429600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:187429200-187430000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:187429800-187430000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:187430000-187437000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr1:187430000-187440000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:187436800-187437000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr1:187436800-187437400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr1:187436800-187437600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr1:187437000-187437400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:187437000-187438600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr1:187437200-187437400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:187437400-187438400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:187437400-187438800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:187437400-187438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:187437600-187438600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr1:187438400-187441600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr1:187438600-187439000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr1:187438600-187439000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr1:187438600-187440400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:187438600-187441000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:187438800-187439200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:187438800-187439400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr1:187438800-187439400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:187438800-187439400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr1:187438800-187440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr1:187439000-187439400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr1:187439200-187440200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr1:187439400-187439800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:187439400-187440600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:187439400-187446200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:187439400-187446400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr1:187439800-187441200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr1:187440000-187440200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:187440200-187440400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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