Variant report

Variant	nsv1001046
Chromosome Location	chr1:158461563-158503338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:158477459-158477489	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:158477392-158477550	K562	blood:	n/a	n/a
3	CEBPB	chr1:158484211-158484348	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr1:158476280-158476430	HCT-116	colon:	n/a	n/a
5	CTCF	chr1:158497080-158497230	NHDF-neo	bronchial:	n/a	n/a
6	CTCF	chr1:158476220-158476370	GM12868	blood:	n/a	n/a
7	CTCF	chr1:158497123-158497273	GM20000	blood:	n/a	n/a
8	CTCF	chr1:158476280-158476430	GM06990	blood:	n/a	n/a
9	CTCF	chr1:158476280-158476430	AG09309	skin:	n/a	n/a
10	CTCF	chr1:158466280-158466430	GM12871	blood:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
11	CTCF	chr1:158497080-158497230	GM12871	blood:	n/a	n/a
12	CTCF	chr1:158476260-158476410	NB4	blood:	n/a	n/a
13	CTCF	chr1:158466297-158466460	Gliobla	brain:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
14	CTCF	chr1:158476260-158476410	AG10803	skin:	n/a	n/a
15	CTCF	chr1:158476260-158476410	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr1:158466320-158466470	GM12869	blood:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
17	CTCF	chr1:158465900-158466050	RPTEC	kidney:	n/a	n/a
18	CTCF	chr1:158466240-158466390	GM12874	blood:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
19	CTCF	chr1:158497073-158497306	LNCaP	prostate:	n/a	n/a
20	CTCF	chr1:158466260-158466410	HUVEC	blood vessel:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
21	CTCF	chr1:158476262-158476437	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:158497120-158497270	HVMF	connective:	n/a	n/a
23	CTCF	chr1:158497034-158497363	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:158497120-158497270	AG10803	skin:	n/a	n/a
25	CTCF	chr1:158466320-158466470	HEK293	kidney:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
26	CTCF	chr1:158476262-158476451	HepG2	liver:	n/a	n/a
27	CTCF	chr1:158496904-158497416	SK-N-SH	brain:	n/a	n/a
28	CTCF	chr1:158497100-158497250	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr1:158497100-158497250	HepG2	liver:	n/a	n/a
30	CTCF	chr1:158497483-158497512	GM10248	blood:	n/a	n/a
31	CTCF	chr1:158466320-158466470	GM12873	blood:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
32	CTCF	chr1:158466300-158466450	HPAF	blood vessel:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
33	CTCF	chr1:158476230-158476467	K562	blood:	n/a	n/a
34	CTCF	chr1:158497080-158497230	GM12872	blood:	n/a	n/a
35	CTCF	chr1:158497077-158497286	HepG2	liver:	n/a	n/a
36	CTCF	chr1:158476260-158476410	Caco-2	colon:	n/a	n/a
37	CTCF	chr1:158497076-158497303	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:158466278-158466443	LNCaP	prostate:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
39	CTCF	chr1:158497026-158497313	Gliobla	brain:	n/a	n/a
40	CTCF	chr1:158497081-158497237	NHEK	skin:	n/a	n/a
41	CTCF	chr1:158497120-158497270	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:158466280-158466430	MCF-7	breast:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
43	CTCF	chr1:158497180-158497330	BE2_C	brain:	n/a	n/a
44	CTCF	chr1:158476232-158476429	HepG2	liver:	n/a	n/a
45	CTCF	chr1:158476240-158476390	GM12866	blood:	n/a	n/a
46	CTCF	chr1:158476300-158476450	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:158476160-158476310	A549	lung:	n/a	n/a
48	CTCF	chr1:158466260-158466410	GM12864	blood:	n/a	chr1:158466361-158466377 chr1:158466355-158466376
49	CTCF	chr1:158476283-158476440	A549	lung:	n/a	n/a
50	CTCF	chr1:158476163-158476602	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158465963-158466013	Hepatocyte	liver:	n/a
2	chr1:158465870-158465920	HMEC	breast:	n/a
3	chr1:158465963-158466013	U87	brain:	n/a
4	chr1:158465870-158465920	IMR90	lung:	fetal
5	chr1:158465963-158466013	ovcar-3	ovarian:	n/a
6	chr1:158465870-158465920	GM12878	blood:	n/a
7	chr1:158465963-158466013	HCM	heart:	n/a
8	chr1:158465870-158465920	NHDF-neo	bronchial:	n/a
9	chr1:158465870-158465920	SK-N-SH_RA	brain:	n/a
10	chr1:158465870-158465920	HAEpiC	amniotic membrane:	n/a
11	chr1:158465963-158466013	NHDF-neo	bronchial:	n/a
12	chr1:158465870-158465920	HCT-116	colon:	n/a
13	chr1:158465870-158465920	PANC-1	pancreas:	n/a
14	chr1:158465870-158465920	Caco-2	colon:	n/a
15	chr1:158465870-158465920	HRPEpiC	eye:	n/a
16	chr1:158465870-158465920	GM06990	blood:	n/a
17	chr1:158465870-158465920	Hela-S3	cervix:	n/a
18	chr1:158465963-158466013	HCPEpiC	choroid plexus:	n/a
19	chr1:158465963-158466013	SK-N-SH	brain:	n/a
20	chr1:158465963-158466013	T-47D	breast:	n/a
21	chr1:158465963-158466013	AG10803	skin:	n/a
22	chr1:158465963-158466013	HNPCEpiC	eye:	n/a
23	chr1:158465963-158466013	NB4	blood:	n/a
24	chr1:158465870-158465920	HL-60	blood:	n/a
25	chr1:158465963-158466013	GM12892	blood:	n/a
26	chr1:158465870-158465920	HepG2	liver:	n/a
27	chr1:158465870-158465920	AG09319	gingival:	n/a
28	chr1:158465963-158466013	NHBE	bronchial:	n/a
29	chr1:158465870-158465920	NT2-D1	testis:	n/a
30	chr1:158465963-158466013	SK-N-MC	brain:	n/a
31	chr1:158465963-158466013	SAEC	small airway:	n/a
32	chr1:158465870-158465920	HRE	kidney:	n/a
33	chr1:158465870-158465920	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:158465870-158465920	HEK293	kidney:	embryo
35	chr1:158465870-158465920	AG04449	skin:	fetal
36	chr1:158465870-158465920	SAEC	small airway:	n/a
37	chr1:158465870-158465920	GM12891	blood:	n/a
38	chr1:158465870-158465920	ECC-1	luminal epithelium:	n/a
39	chr1:158465963-158466013	LNCaP	prostate:	n/a
40	chr1:158465963-158466013	SKMC	muscle:	n/a
41	chr1:158465963-158466013	IMR90	lung:	fetal
42	chr1:158465963-158466013	Caco-2	colon:	n/a
43	chr1:158465870-158465920	CMK	blood:	n/a
44	chr1:158465963-158466013	K562	blood:	n/a
45	chr1:158465870-158465920	HEEpiC	esophagus:	n/a
46	chr1:158465963-158466013	GM19239	blood:	n/a
47	chr1:158465870-158465920	PrEC	prostate:	n/a
48	chr1:158465870-158465920	AG09309	skin:	n/a
49	chr1:158465963-158466013	BJ	skin:	n/a
50	chr1:158465963-158466013	BE2_C	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158173492..158174259-chr1:158466062..158466855,4	MCF-7	breast:
2	chr1:158473786..158476018-chr1:158544430..158546259,2	K562	blood:
3	chr1:158476296..158476820-chr1:158968188..158969128,2	K562	blood:
4	chr1:158216395..158217146-chr1:158496757..158497397,2	MCF-7	breast:
5	chr1:158475878..158476640-chr1:158968361..158968916,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR6Y1-1	chr1:158464192-158464344	ENSG00000236656.1
2	lnc-OR6Y1-1	chr1:158464445-158464507	ENSG00000236656.1
3	lnc-OR10R2-1	chr1:158484575-158485715	NONHSAT006988

No data

Variant related genes	Relation type
OR10R1P	TF binding region
ENSG00000231434	TF binding region
ENSG00000236656	TF binding region
OR10R1P	CpG island
ENSG00000231434	CpG island
ENSG00000236656	CpG island
ENSG00000176320	chromatin interactions

Extended variants
information (count: 769 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1873509	chr1:158461563-158461564	Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533639743	chr1:158461577-158461578	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs574845924	chr1:158461592-158461593	Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs79703471	chr1:158461608-158461609	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs554433615	chr1:158461628-158461629	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs572748492	chr1:158461671-158461672	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs540014899	chr1:158461705-158461706	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs559829846	chr1:158461731-158461732	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs533280136	chr1:158461748-158461749	Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs112121816	chr1:158461806-158461807	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs189930824	chr1:158461887-158461888	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs4356044	chr1:158461888-158461889	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181478090	chr1:158461941-158461942	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs949397	chr1:158461951-158461952	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs949398	chr1:158461983-158461984	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187001222	chr1:158461989-158461990	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191930370	chr1:158461990-158461991	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183390094	chr1:158462014-158462015	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs114586021	chr1:158462061-158462062	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs185022699	chr1:158462081-158462082	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs78755674	chr1:158462085-158462086	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs568551472	chr1:158462157-158462158	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11264983	chr1:158462218-158462219	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140544469	chr1:158462238-158462239	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs568018699	chr1:158462282-158462283	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs78831700	chr1:158462302-158462303	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533454279	chr1:158462316-158462317	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369377874	chr1:158462348-158462349	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs558493153	chr1:158462430-158462431	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs6664542	chr1:158462431-158462432	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189582239	chr1:158462458-158462459	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs150491140	chr1:158462470-158462471	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs6689657	chr1:158462509-158462510	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570452082	chr1:158462519-158462520	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs138321558	chr1:158462544-158462545	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561603520	chr1:158462560-158462561	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182273249	chr1:158462561-158462562	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs200878198	chr1:158462583-158462584	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs142594298	chr1:158462601-158462602	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs114928692	chr1:158462611-158462612	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs532729494	chr1:158462620-158462621	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs550449325	chr1:158462671-158462672	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs879637	chr1:158462697-158462698	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535876725	chr1:158462722-158462723	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs879636	chr1:158462797-158462798	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs74707842	chr1:158462798-158462799	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs902637	chr1:158462840-158462841	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369577335	chr1:158462878-158462879	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs555544395	chr1:158462890-158462891	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs577006035	chr1:158462902-158462903	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158457400-158461600	Active TSS	Thymus	Thymus
2	chr1:158458400-158465000	Flanking Active TSS	Dnd41	blood
3	chr1:158461400-158461800	Flanking Active TSS	Fetal Thymus	thymus
4	chr1:158461600-158461800	Transcr. at gene 5' and 3'	Thymus	Thymus
5	chr1:158461800-158465200	Active TSS	Fetal Thymus	thymus
6	chr1:158461800-158465800	Active TSS	Thymus	Thymus
7	chr1:158465000-158465400	Enhancers	Dnd41	blood
8	chr1:158465200-158465800	Weak transcription	Fetal Thymus	thymus
9	chr1:158465400-158466200	Flanking Active TSS	Dnd41	blood
10	chr1:158465800-158466000	Flanking Active TSS	Thymus	Thymus
11	chr1:158465800-158466200	Enhancers	Fetal Thymus	thymus
12	chr1:158466000-158466400	Active TSS	Thymus	Thymus
13	chr1:158466200-158467200	Enhancers	Dnd41	blood
14	chr1:158478800-158479000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:158479000-158479600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:158479600-158480000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr1:158479600-158480200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:158479600-158480200	Enhancers	Fetal Stomach	stomach
19	chr1:158480000-158480800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr1:158486000-158486600	Enhancers	Brain Cingulate Gyrus	brain
21	chr1:158486800-158487000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:158486800-158487800	Enhancers	Brain Hippocampus Middle	brain
23	chr1:158489400-158489600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:158490800-158491000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:158490800-158492000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:158491000-158491200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:158491000-158491600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr1:158491000-158491600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:158491000-158491800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:158491600-158491800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr1:158491600-158492000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr1:158491800-158496800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:158491800-158497400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:158492000-158497200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:158495800-158497400	Enhancers	Dnd41	blood
36	chr1:158496800-158498200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr1:158497000-158498000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr1:158497200-158497600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:158497200-158498000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr1:158497400-158497600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr1:158497400-158498000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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