Variant report

Variant	nsv872632
Chromosome Location	chr1:188802542-188931828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:188818322-188818328	K562	blood:	n/a	n/a
2	ATF1	chr1:188884384-188884432	K562	blood:	n/a	n/a
3	BRCA1	chr1:188857430-188857935	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:188908515-188909072	HepG2	liver:	n/a	chr1:188908639-188908650
5	CEBPB	chr1:188861151-188861446	A549	lung:	n/a	chr1:188861298-188861309
6	CEBPB	chr1:188857462-188857804	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:188908490-188909077	A549	lung:	n/a	chr1:188908639-188908650
8	CEBPB	chr1:188861137-188861478	HepG2	liver:	n/a	chr1:188861298-188861309
9	CEBPB	chr1:188833745-188833994	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:188854862-188855129	HepG2	liver:	n/a	chr1:188854961-188854974 chr1:188854963-188854974 chr1:188854961-188854972 chr1:188854961-188854974
11	CEBPB	chr1:188908501-188909140	IMR90	lung:	n/a	chr1:188908639-188908650
12	CEBPB	chr1:188845139-188845339	HepG2	liver:	n/a	chr1:188845215-188845226 chr1:188845214-188845227
13	CEBPB	chr1:188861165-188861434	K562	blood:	n/a	chr1:188861298-188861309
14	CEBPB	chr1:188861237-188861445	H1-hESC	embryonic stem cell:	n/a	chr1:188861298-188861309
15	CEBPB	chr1:188857286-188858045	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:188861142-188861475	Hela-S3	cervix:	n/a	chr1:188861298-188861309
17	CEBPB	chr1:188918872-188919227	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:188861120-188861477	IMR90	lung:	n/a	chr1:188861298-188861309
19	CHD2	chr1:188857543-188857987	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr1:188911366-188911566	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:188873380-188873674	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr1:188907460-188907610	HCT-116	colon:	n/a	n/a
23	CTCF	chr1:188907380-188907530	AG04449	skin:	n/a	n/a
24	CTCF	chr1:188907340-188907490	GM12865	blood:	n/a	n/a
25	CTCF	chr1:188907400-188907550	NB4	blood:	n/a	n/a
26	CTCF	chr1:188907400-188907550	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr1:188913689-188913825	Medullo	brain:	n/a	n/a
28	CTCF	chr1:188927711-188927864	GM12878	blood:	n/a	n/a
29	CTCF	chr1:188907379-188907587	Gliobla	brain:	n/a	n/a
30	CTCF	chr1:188907420-188907570	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr1:188899890-188899962	GM20000	blood:	n/a	n/a
32	CTCF	chr1:188913700-188913850	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:188927619-188927953	GM12878	blood:	n/a	n/a
34	CTCF	chr1:188913709-188913929	GM12878	blood:	n/a	n/a
35	CTCF	chr1:188881453-188881600	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr1:188907380-188907530	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:188907380-188907530	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:188881460-188881610	HRE	kidney:	n/a	n/a
39	CTCF	chr1:188907420-188907570	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr1:188907420-188907570	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:188927761-188927790	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr1:188907380-188907530	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:188907480-188907630	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr1:188913540-188913690	BE2_C	brain:	n/a	n/a
45	CTCF	chr1:188927620-188927770	GM12871	blood:	n/a	n/a
46	CTCF	chr1:188907340-188907490	HCM	heart:	n/a	n/a
47	CTCF	chr1:188907400-188907550	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr1:188907230-188907682	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:188907410-188907550	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:188907408-188907599	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:188826823-188826873	HIPEpiC	eye:	n/a
2	chr1:188826823-188826873	SK-N-MC	brain:	n/a
3	chr1:188826823-188826873	AG10803	skin:	n/a
4	chr1:188826823-188826873	T-47D	breast:	n/a
5	chr1:188826889-188826939	AG04450	lung:	fetal
6	chr1:188826823-188826873	A549	lung:	n/a
7	chr1:188826889-188826939	AG04449	skin:	fetal
8	chr1:188826889-188826939	SK-N-MC	brain:	n/a
9	chr1:188826823-188826873	PFSK-1	brain:	n/a
10	chr1:188826823-188826873	SK-N-SH	brain:	n/a
11	chr1:188826823-188826873	NB4	blood:	n/a
12	chr1:188826889-188826939	GM12892	blood:	n/a
13	chr1:188826889-188826939	A549	lung:	n/a
14	chr1:188826889-188826939	HEK293	kidney:	embryo
15	chr1:188826889-188826939	AG09319	gingival:	n/a
16	chr1:188826823-188826873	AG09319	gingival:	n/a
17	chr1:188826889-188826939	HCPEpiC	choroid plexus:	n/a
18	chr1:188826823-188826873	HepG2	liver:	n/a
19	chr1:188826889-188826939	Hela-S3	cervix:	n/a
20	chr1:188826889-188826939	NT2-D1	testis:	n/a
21	chr1:188826823-188826873	NHBE	bronchial:	n/a
22	chr1:188826889-188826939	GM06990	blood:	n/a
23	chr1:188826889-188826939	HIPEpiC	eye:	n/a
24	chr1:188826889-188826939	MCF10A-Er-Src	breast:	n/a
25	chr1:188826823-188826873	LNCaP	prostate:	n/a
26	chr1:188826823-188826873	AG04449	skin:	fetal
27	chr1:188826823-188826873	HCPEpiC	choroid plexus:	n/a
28	chr1:188826823-188826873	MCF10A-Er-Src	breast:	n/a
29	chr1:188826889-188826939	ovcar-3	ovarian:	n/a
30	chr1:188826823-188826873	RPTEC	kidney:	n/a
31	chr1:188826889-188826939	RPTEC	kidney:	n/a
32	chr1:188826823-188826873	NH-A	brain:	n/a
33	chr1:188826823-188826873	H1-hESC	embryonic stem cell:	embryo
34	chr1:188826823-188826873	PrEC	prostate:	n/a
35	chr1:188826823-188826873	U87	brain:	n/a
36	chr1:188826823-188826873	AG09309	skin:	n/a
37	chr1:188826889-188826939	HRPEpiC	eye:	n/a
38	chr1:188826823-188826873	NT2-D1	testis:	n/a
39	chr1:188826889-188826939	HL-60	blood:	n/a
40	chr1:188826823-188826873	HEEpiC	esophagus:	n/a
41	chr1:188826889-188826939	CMK	blood:	n/a
42	chr1:188826889-188826939	PFSK-1	brain:	n/a
43	chr1:188826823-188826873	PANC-1	pancreas:	n/a
44	chr1:188826889-188826939	HepG2	liver:	n/a
45	chr1:188826823-188826873	Hela-S3	cervix:	n/a
46	chr1:188826823-188826873	HNPCEpiC	eye:	n/a
47	chr1:188826823-188826873	GM12891	blood:	n/a
48	chr1:188826823-188826873	GM06990	blood:	n/a
49	chr1:188826889-188826939	BE2_C	brain:	n/a
50	chr1:188826823-188826873	ECC-1	luminal epithelium:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:188899689..188901909-chr1:188904686..188906688,2	K562	blood:
2	chr1:188899689..188901909-chr1:188904686..188906688,2	K562	blood:
3	chr1:188917480..188919329-chr1:188920804..188923130,2	MCF-7	breast:
4	chr1:188751121..188751789-chr1:188907053..188907934,3	MCF-7	breast:
5	chr1:188846061..188848491-chr1:188851171..188853585,2	MCF-7	breast:
6	chr1:188458178..188458728-chr1:188906958..188907936,3	MCF-7	breast:
7	chr1:188401580..188402198-chr1:188862429..188863519,3	MCF-7	breast:
8	chr1:188902220..188904596-chr1:189118871..189120838,2	K562	blood:
9	chr1:188896826..188898736-chr1:188903150..188906844,3	MCF-7	breast:
10	chr1:188917480..188919329-chr1:188920804..188923130,2	MCF-7	breast:
11	chr1:188866159..188868933-chr1:188870871..188872423,2	MCF-7	breast:
12	chr1:188896826..188898736-chr1:188903150..188906844,3	MCF-7	breast:
13	chr1:188788862..188791265-chr1:188817309..188819818,2	MCF-7	breast:
14	chr1:188866159..188868933-chr1:188870871..188872423,2	MCF-7	breast:
15	chr1:188846061..188848491-chr1:188851171..188853585,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-6	chr1:188874819-188875057	ENSG00000226486
2	lnc-PLA2G4A-17	chr1:188860643-188860786	refGeneNc_416_NR_033922
3	lnc-FAM5C-2	chr1:188838608-188838879	XLOC_001129
4	lnc-FAM5C-2	chr1:188856372-188856565	XLOC_001129

No data

Variant related genes	Relation type
LINC01035	TF binding region
ENSG00000238054	TF binding region
LINC01035	CpG island
ENSG00000238054	CpG island
KIAA0494	miRNA target sites

Extended variants
information (count: 1623 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545109250	chr1:188812205-188812206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7548983	chr1:188812287-188812288	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs189570968	chr1:188812297-188812298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73068782	chr1:188812369-188812370	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370064266	chr1:188812459-188812460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372728864	chr1:188812460-188812461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529948246	chr1:188812549-188812550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375026532	chr1:188812557-188812558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75730299	chr1:188812564-188812565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537380735	chr1:188812571-188812572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146037269	chr1:188812606-188812607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78916713	chr1:188812631-188812632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181277902	chr1:188812640-188812641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375006964	chr1:188812649-188812650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11811064	chr1:188812655-188812656	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34807144	chr1:188812663-188812664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548603273	chr1:188812723-188812724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568421708	chr1:188812736-188812737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534509140	chr1:188812797-188812798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs118018029	chr1:188812813-188812814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11810709	chr1:188812874-188812875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75637922	chr1:188812893-188812894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76440077	chr1:188812920-188812921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76812487	chr1:188812986-188812987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184322551	chr1:188813097-188813098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372911301	chr1:188813121-188813122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188924345	chr1:188813142-188813143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181616614	chr1:188813154-188813155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539823312	chr1:188813221-188813222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560223729	chr1:188813234-188813235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532429955	chr1:188813260-188813261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552136587	chr1:188813304-188813305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562653512	chr1:188813350-188813351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187236120	chr1:188813378-188813379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542006204	chr1:188813389-188813390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548666650	chr1:188813420-188813421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191904732	chr1:188813436-188813437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6692124	chr1:188813513-188813514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182491057	chr1:188813524-188813525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571098497	chr1:188813538-188813539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540122311	chr1:188813544-188813545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138826557	chr1:188813558-188813559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185934427	chr1:188813575-188813576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570197371	chr1:188813594-188813595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537573785	chr1:188813599-188813600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562139713	chr1:188813621-188813622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189872213	chr1:188813656-188813657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574181092	chr1:188813683-188813684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559683289	chr1:188813701-188813702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553727462	chr1:188813744-188813745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
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
Trisomy 5 syndrome	21098271	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:188812200-188812600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:188812200-188813000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:188812400-188813000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:188812800-188813000	Enhancers	Pancreas	Pancrea
5	chr1:188813000-188815600	Weak transcription	Pancreas	Pancrea
6	chr1:188815600-188816000	ZNF genes & repeats	Pancreas	Pancrea
7	chr1:188815800-188816000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:188819600-188820400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr1:188820400-188821400	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr1:188820600-188820800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:188823800-188824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr1:188823800-188824600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr1:188824200-188824600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:188826600-188826800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:188826600-188827000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:188826600-188827200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:188826800-188827000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:188827000-188827200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:188835000-188835400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:188846600-188847200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:188846600-188847600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:188854400-188855000	Enhancers	Hela-S3	cervix
23	chr1:188855000-188855800	Weak transcription	Hela-S3	cervix
24	chr1:188855800-188856400	Enhancers	Hela-S3	cervix
25	chr1:188856400-188857600	Flanking Active TSS	Hela-S3	cervix
26	chr1:188857200-188858000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:188857600-188859200	Weak transcription	Hela-S3	cervix
28	chr1:188859200-188859600	Enhancers	Hela-S3	cervix
29	chr1:188869600-188869800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr1:188869800-188872000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr1:188872000-188872200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr1:188872200-188873000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr1:188873000-188874000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr1:188873200-188873600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr1:188873200-188873800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:188873400-188873800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr1:188873400-188873800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:188873400-188873800	Enhancers	Hela-S3	cervix
39	chr1:188873400-188874000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:188873400-188874000	Enhancers	Fetal Intestine Large	intestine
41	chr1:188883800-188884600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr1:188884200-188884600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:188897800-188898400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:188898000-188898400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:188898000-188898400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:188898000-188898600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:188898200-188898600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr1:188898400-188910800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr1:188901800-188902400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:188907000-188907400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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