Variant report

Variant	nsv997904
Chromosome Location	chr1:225389490-225466637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225396825-225397387	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225416534-225417017	HepG2	liver:	n/a	n/a
3	ATF2	chr1:225438070-225438415	GM12878	blood:	n/a	n/a
4	BATF	chr1:225438147-225438493	GM12878	blood:	n/a	n/a
5	BATF	chr1:225438165-225438534	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:225438166-225438412	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:225438111-225438466	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:225438084-225438466	GM12878	blood:	n/a	n/a
9	CEBPB	chr1:225466364-225466580	HepG2	liver:	n/a	chr1:225466481-225466494 chr1:225466481-225466494 chr1:225466483-225466494 chr1:225466481-225466492
10	CEBPB	chr1:225447251-225447411	HepG2	liver:	n/a	chr1:225447297-225447308
11	CEBPB	chr1:225417884-225418049	HepG2	liver:	n/a	chr1:225417940-225417951
12	CEBPB	chr1:225424526-225424624	A549	lung:	n/a	n/a
13	CEBPB	chr1:225412593-225412887	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:225417850-225417972	IMR90	lung:	n/a	chr1:225417940-225417951
15	CEBPB	chr1:225464505-225464691	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:225396821-225397186	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:225459947-225460000	A549	lung:	n/a	n/a
18	CEBPZ	chr1:225416674-225416952	HepG2	liver:	n/a	n/a
19	CHD2	chr1:225438181-225438501	GM12878	blood:	n/a	n/a
20	CTCF	chr1:225441065-225441136	HepG2	liver:	n/a	n/a
21	CTCF	chr1:225440980-225441130	GM12864	blood:	n/a	n/a
22	CTCF	chr1:225447921-225447981	GM20000	blood:	n/a	n/a
23	CTCF	chr1:225440980-225441130	BE2_C	brain:	n/a	n/a
24	CTCF	chr1:225441040-225441190	GM12867	blood:	n/a	n/a
25	CTCF	chr1:225441020-225441170	GM12873	blood:	n/a	n/a
26	CTCF	chr1:225390860-225391010	NHLF	lung:	n/a	n/a
27	CTCF	chr1:225441000-225441150	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:225441040-225441190	GM06990	blood:	n/a	n/a
29	CTCF	chr1:225441000-225441150	GM06990	blood:	n/a	n/a
30	CTCF	chr1:225441000-225441150	HMF	breast:	n/a	n/a
31	CTCF	chr1:225440920-225441070	GM12869	blood:	n/a	n/a
32	CTCF	chr1:225440960-225441110	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr1:225440980-225441130	HCFaa	heart:	n/a	n/a
34	CTCF	chr1:225438637-225438658	Lung_OC	lung:	n/a	n/a
35	CTCF	chr1:225441000-225441150	GM12875	blood:	n/a	n/a
36	CTCF	chr1:225433776-225433885	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr1:225441000-225441150	GM12873	blood:	n/a	n/a
38	CTCF	chr1:225440980-225441130	K562	blood:	n/a	n/a
39	CTCF	chr1:225441060-225441210	HMEC	breast:	n/a	n/a
40	CTCF	chr1:225441031-225441162	K562	blood:	n/a	n/a
41	CTCF	chr1:225441060-225441210	HMF	breast:	n/a	n/a
42	CTCF	chr1:225441040-225441190	GM12872	blood:	n/a	n/a
43	CTCF	chr1:225441080-225441230	GM12872	blood:	n/a	n/a
44	CTCF	chr1:225415471-225415556	GM20000	blood:	n/a	n/a
45	CTCF	chr1:225461069-225461111	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr1:225440960-225441110	AG10803	skin:	n/a	n/a
47	CTCF	chr1:225448944-225449026	GM13976	blood:	n/a	n/a
48	CTCF	chr1:225440940-225441090	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:225441000-225441150	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:225411000-225411150	GM12872	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225427173-225427223	MCF-7	breast:	n/a
2	chr1:225427173-225427223	MCF10A-Er-Src	breast:	n/a
3	chr1:225427173-225427223	LNCaP	prostate:	n/a
4	chr1:225427173-225427223	SAEC	small airway:	n/a
5	chr1:225427173-225427223	AG10803	skin:	n/a
6	chr1:225427173-225427223	HRPEpiC	eye:	n/a
7	chr1:225427173-225427223	NH-A	brain:	n/a
8	chr1:225427173-225427223	HL-60	blood:	n/a
9	chr1:225427173-225427223	HRCEpiC	kidney:	n/a
10	chr1:225427173-225427223	BJ	skin:	n/a
11	chr1:225427173-225427223	ECC-1	luminal epithelium:	n/a
12	chr1:225427173-225427223	SK-N-SH	brain:	n/a
13	chr1:225427173-225427223	GM12892	blood:	n/a
14	chr1:225427173-225427223	NHDF-neo	bronchial:	n/a
15	chr1:225427173-225427223	PFSK-1	brain:	n/a
16	chr1:225427173-225427223	HNPCEpiC	eye:	n/a
17	chr1:225427173-225427223	HUVEC	blood vessel:	n/a
18	chr1:225427173-225427223	HCPEpiC	choroid plexus:	n/a
19	chr1:225427173-225427223	SKMC	muscle:	n/a
20	chr1:225427173-225427223	GM06990	blood:	n/a
21	chr1:225427173-225427223	H1-hESC	embryonic stem cell:	embryo
22	chr1:225427173-225427223	SK-N-MC	brain:	n/a
23	chr1:225427173-225427223	RPTEC	kidney:	n/a
24	chr1:225427173-225427223	NHBE	bronchial:	n/a
25	chr1:225427173-225427223	Hepatocyte	liver:	n/a
26	chr1:225427173-225427223	HCM	heart:	n/a
27	chr1:225427173-225427223	AG04450	lung:	fetal
28	chr1:225427173-225427223	ProgFib	skin:	n/a
29	chr1:225427173-225427223	PANC-1	pancreas:	n/a
30	chr1:225427173-225427223	HEEpiC	esophagus:	n/a
31	chr1:225427173-225427223	AoSMC	blood vessel:	n/a
32	chr1:225427173-225427223	A549	lung:	n/a
33	chr1:225427173-225427223	GM19239	blood:	n/a
34	chr1:225427173-225427223	HIPEpiC	eye:	n/a
35	chr1:225427173-225427223	T-47D	breast:	n/a
36	chr1:225427173-225427223	GM12891	blood:	n/a
37	chr1:225427173-225427223	AG09319	gingival:	n/a
38	chr1:225427173-225427223	NT2-D1	testis:	n/a
39	chr1:225427173-225427223	GM12878	blood:	n/a
40	chr1:225427173-225427223	HCF	heart:	n/a
41	chr1:225427173-225427223	CMK	blood:	n/a
42	chr1:225427173-225427223	IMR90	lung:	fetal
43	chr1:225427173-225427223	HRE	kidney:	n/a
44	chr1:225427173-225427223	Caco-2	colon:	n/a
45	chr1:225427173-225427223	Jurkat	blood:	n/a
46	chr1:225427173-225427223	HCT-116	colon:	n/a
47	chr1:225427173-225427223	AG09309	skin:	n/a
48	chr1:225427173-225427223	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:225427173-225427223	HEK293	kidney:	embryo
50	chr1:225427173-225427223	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:225465995..225468148-chr1:225470406..225472141,2	K562	blood:

No data

Variant related genes	Relation type
DNAH14	TF binding region
DNAH14	CpG island

Extended variants
information (count: 1573 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1573 , 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	rs4308947	chr1:225389490-225389491	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181919409	chr1:225389495-225389496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186284135	chr1:225389496-225389497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575825773	chr1:225389512-225389513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546017230	chr1:225389560-225389561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35342713	chr1:225389575-225389576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71170065	chr1:225389576-225389577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397983028	chr1:225389594-225389595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191041928	chr1:225389634-225389635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528729159	chr1:225389644-225389645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547166257	chr1:225389680-225389681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12092293	chr1:225389698-225389699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529495089	chr1:225389699-225389700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142428668	chr1:225389700-225389701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543172944	chr1:225389785-225389786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568478537	chr1:225389799-225389800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10915798	chr1:225389868-225389869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs182883239	chr1:225389873-225389874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566558465	chr1:225389884-225389885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187479585	chr1:225389948-225389949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112187382	chr1:225389994-225389995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375258086	chr1:225390012-225390013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10915799	chr1:225390030-225390031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191127172	chr1:225390047-225390048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575738573	chr1:225390146-225390147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546177744	chr1:225390179-225390180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1842335	chr1:225390183-225390184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs531621952	chr1:225390199-225390200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12410126	chr1:225390233-225390234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs34185159	chr1:225390234-225390235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116784876	chr1:225390248-225390249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367859544	chr1:225390249-225390250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529556810	chr1:225390295-225390296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550894422	chr1:225390305-225390306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183343771	chr1:225390306-225390307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138706216	chr1:225390320-225390321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12406388	chr1:225390334-225390335	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs376436533	chr1:225390351-225390352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551347860	chr1:225390362-225390363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149340600	chr1:225390384-225390385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533858015	chr1:225390385-225390386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143666565	chr1:225390728-225390729	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs11584486	chr1:225390734-225390735	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187509767	chr1:225390752-225390753	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs138453293	chr1:225390753-225390754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs112485689	chr1:225390780-225390781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs192720377	chr1:225390813-225390814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550371021	chr1:225390822-225390823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570271184	chr1:225390855-225390856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555423792	chr1:225390859-225390860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	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
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
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225389000-225389600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:225389600-225390200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:225390200-225390400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:225390600-225390800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
5	chr1:225390800-225395600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:225391400-225392800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:225391600-225395400	Weak transcription	Ovary	ovary
8	chr1:225392400-225396200	Weak transcription	Liver	Liver
9	chr1:225392800-225393000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:225392800-225393000	ZNF genes & repeats	Pancreas	Pancrea
11	chr1:225393000-225397400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:225393000-225397400	Weak transcription	Pancreas	Pancrea
13	chr1:225395200-225399200	Enhancers	HepG2	liver
14	chr1:225395400-225395600	ZNF genes & repeats	Ovary	ovary
15	chr1:225395600-225396200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
16	chr1:225395600-225397400	Weak transcription	Ovary	ovary
17	chr1:225397400-225397800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:225397400-225397800	ZNF genes & repeats	Pancreas	Pancrea
19	chr1:225397400-225398000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:225397400-225398000	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr1:225397400-225398000	Strong transcription	Ovary	ovary
22	chr1:225397600-225398000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:225398000-225400000	Weak transcription	Ovary	ovary
24	chr1:225398000-225404800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:225398000-225417800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:225404800-225406000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:225405200-225405600	ZNF genes & repeats	Pancreas	Pancrea
28	chr1:225405400-225406600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:225406600-225409400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:225409400-225410000	Enhancers	HepG2	liver
31	chr1:225409400-225411600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:225410000-225415200	Weak transcription	HepG2	liver
33	chr1:225411200-225412800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:225411600-225413600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:225412400-225412600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:225412400-225412800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:225412400-225414000	Enhancers	Placenta	Placenta
38	chr1:225412600-225413200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:225412800-225413600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:225412800-225414600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr1:225413200-225414200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:225413600-225413800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:225413600-225414000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:225414000-225415800	Weak transcription	Placenta	Placenta
45	chr1:225414000-225416000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:225414200-225415200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:225414600-225414800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:225414800-225415000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:225415200-225416600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:225415200-225417200	Enhancers	HepG2	liver

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