Variant report

Variant	esv3522877
Chromosome Location	chr1:189728929-189784677
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:189743917-189744230	HepG2	liver:	n/a	n/a
2	ATF1	chr1:189759191-189759268	K562	blood:	n/a	n/a
3	BACH1	chr1:189774960-189775194	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr1:189743704-189744394	A549	lung:	n/a	chr1:189744338-189744347
5	CEBPB	chr1:189743808-189744388	MCF-7	breast:	n/a	chr1:189743903-189743914
6	CEBPB	chr1:189738671-189738934	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:189743808-189744409	A549	lung:	n/a	chr1:189743903-189743914
8	CEBPB	chr1:189738746-189738942	A549	lung:	n/a	n/a
9	CEBPB	chr1:189738620-189739003	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:189743902-189744361	MCF-7	breast:	n/a	chr1:189743903-189743914
11	CEBPB	chr1:189769228-189769482	HepG2	liver:	n/a	chr1:189769331-189769342 chr1:189769332-189769343
12	CEBPB	chr1:189769201-189769380	A549	lung:	n/a	chr1:189769331-189769342 chr1:189769332-189769343
13	CEBPB	chr1:189731505-189731602	K562	blood:	n/a	chr1:189731575-189731586
14	CEBPB	chr1:189738790-189738826	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:189731420-189731730	HepG2	liver:	n/a	chr1:189731575-189731586
16	CEBPB	chr1:189739895-189740150	A549	lung:	n/a	n/a
17	CTCF	chr1:189745863-189745931	GM20000	blood:	n/a	n/a
18	CTCF	chr1:189772560-189772710	BE2_C	brain:	n/a	n/a
19	CTCF	chr1:189772580-189772730	GM12873	blood:	n/a	n/a
20	CTCF	chr1:189772640-189772790	HEK293	kidney:	n/a	n/a
21	CTCF	chr1:189772620-189772770	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr1:189772600-189772750	GM12868	blood:	n/a	n/a
23	CTCF	chr1:189772620-189772770	A549	lung:	n/a	n/a
24	CTCF	chr1:189756934-189756961	GM10248	blood:	n/a	n/a
25	CTCF	chr1:189772620-189772770	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr1:189750940-189751090	HAc	cerebellar:	n/a	n/a
27	CTCF	chr1:189772620-189772770	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:189772600-189772750	RPTEC	kidney:	n/a	n/a
29	CTCF	chr1:189772555-189772759	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:189772560-189772710	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:189772560-189772710	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr1:189772620-189772770	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:189747632-189747687	GM13976	blood:	n/a	n/a
34	CTCF	chr1:189772600-189772750	GM12872	blood:	n/a	n/a
35	CTCF	chr1:189738460-189738610	AG04450	lung:	n/a	n/a
36	CTCF	chr1:189772660-189772810	HCT-116	colon:	n/a	n/a
37	CTCF	chr1:189772620-189772770	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr1:189772560-189772710	GM12873	blood:	n/a	n/a
39	CTCF	chr1:189772600-189772750	HRE	kidney:	n/a	n/a
40	CTCF	chr1:189772580-189772730	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:189772540-189772690	GM12866	blood:	n/a	n/a
42	CTCF	chr1:189772620-189772770	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr1:189772640-189772790	HCT-116	colon:	n/a	n/a
44	E2F4	chr1:189768760-189768855	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr1:189730467-189730667	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr1:189765605-189765610	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr1:189776518-189776660	MCF10A-Er-Src	breast:	n/a	n/a
48	ELF1	chr1:189743680-189744925	MCF-7	breast:	n/a	n/a
49	EP300	chr1:189743740-189744465	A549	lung:	n/a	chr1:189744371-189744385
50	EP300	chr1:189751453-189751695	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189744005-189744055	HMEC	breast:	n/a
2	chr1:189744005-189744055	PrEC	prostate:	n/a
3	chr1:189744005-189744055	GM12878	blood:	n/a
4	chr1:189744005-189744055	HCPEpiC	choroid plexus:	n/a
5	chr1:189744005-189744055	HRPEpiC	eye:	n/a
6	chr1:189744005-189744055	Hela-S3	cervix:	n/a
7	chr1:189744005-189744055	SAEC	small airway:	n/a
8	chr1:189744005-189744055	SK-N-SH	brain:	n/a
9	chr1:189744005-189744055	MCF-7	breast:	n/a
10	chr1:189744005-189744055	HAEpiC	amniotic membrane:	n/a
11	chr1:189744005-189744055	Hepatocyte	liver:	n/a
12	chr1:189744005-189744055	H1-hESC	embryonic stem cell:	embryo
13	chr1:189744005-189744055	HCM	heart:	n/a
14	chr1:189744005-189744055	HL-60	blood:	n/a
15	chr1:189744005-189744055	AG04449	skin:	fetal
16	chr1:189744005-189744055	NHDF-neo	bronchial:	n/a
17	chr1:189744005-189744055	IMR90	lung:	fetal
18	chr1:189744005-189744055	HRCEpiC	kidney:	n/a
19	chr1:189744005-189744055	HRE	kidney:	n/a
20	chr1:189744005-189744055	ProgFib	skin:	n/a
21	chr1:189744005-189744055	A549	lung:	n/a
22	chr1:189744005-189744055	K562	blood:	n/a
23	chr1:189744005-189744055	BJ	skin:	n/a
24	chr1:189744005-189744055	HCT-116	colon:	n/a
25	chr1:189744005-189744055	PFSK-1	brain:	n/a
26	chr1:189744005-189744055	AG10803	skin:	n/a
27	chr1:189744005-189744055	Caco-2	colon:	n/a
28	chr1:189744005-189744055	ovcar-3	ovarian:	n/a
29	chr1:189744005-189744055	LNCaP	prostate:	n/a
30	chr1:189744005-189744055	NB4	blood:	n/a
31	chr1:189744005-189744055	AG09319	gingival:	n/a
32	chr1:189744005-189744055	SK-N-SH_RA	brain:	n/a
33	chr1:189744005-189744055	HCF	heart:	n/a
34	chr1:189744005-189744055	AoSMC	blood vessel:	n/a
35	chr1:189744005-189744055	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:189744005-189744055	BE2_C	brain:	n/a
37	chr1:189744005-189744055	GM19239	blood:	n/a
38	chr1:189744005-189744055	GM12891	blood:	n/a
39	chr1:189744005-189744055	T-47D	breast:	n/a
40	chr1:189744005-189744055	SKMC	muscle:	n/a
41	chr1:189744005-189744055	RPTEC	kidney:	n/a
42	chr1:189744005-189744055	HEEpiC	esophagus:	n/a
43	chr1:189744005-189744055	NHBE	bronchial:	n/a
44	chr1:189744005-189744055	GM06990	blood:	n/a
45	chr1:189744005-189744055	MCF10A-Er-Src	breast:	n/a
46	chr1:189744005-189744055	SK-N-MC	brain:	n/a
47	chr1:189744005-189744055	CMK	blood:	n/a
48	chr1:189744005-189744055	PANC-1	pancreas:	n/a
49	chr1:189744005-189744055	Jurkat	blood:	n/a
50	chr1:189744005-189744055	NT2-D1	testis:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
2	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
3	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
4	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
5	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:
6	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
7	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-7	chr1:189746390-189746467	XLOC_000503
2	lnc-RGS18-7	chr1:189783962-189784048	XLOC_000503
3	lnc-RGS18-7	chr1:189760709-189760893	XLOC_000503
4	lnc-RGS18-7	chr1:189744595-189744695	XLOC_000503

No data

Variant related genes	Relation type
ENSG00000232212	TF binding region
ENSG00000232212	CpG island
SOX11	miRNA target sites
SOX13	miRNA target sites
SOX2	miRNA target sites

Extended variants
information (count: 684 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139333087	chr1:189733201-189733202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368393967	chr1:189733266-189733267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540530649	chr1:189733287-189733288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143030465	chr1:189733308-189733309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187412908	chr1:189733341-189733342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189814265	chr1:189733486-189733487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567248564	chr1:189733505-189733506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568401964	chr1:189733512-189733513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200937912	chr1:189733563-189733564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552585060	chr1:189733610-189733611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147463346	chr1:189733623-189733624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372235756	chr1:189733634-189733635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558627299	chr1:189733693-189733694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575201610	chr1:189733710-189733711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544811420	chr1:189733725-189733726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554830838	chr1:189733754-189733755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114490722	chr1:189733784-189733785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547214674	chr1:189733830-189733831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202144895	chr1:189733867-189733868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76676751	chr1:189733868-189733869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182129699	chr1:189733896-189733897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115518787	chr1:189733924-189733925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532543631	chr1:189733963-189733964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1339446	chr1:189733979-189733980	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185319443	chr1:189734010-189734011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190130291	chr1:189734045-189734046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550767864	chr1:189734181-189734182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183062836	chr1:189734192-189734193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529966350	chr1:189734212-189734213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546488270	chr1:189734275-189734276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369117887	chr1:189734325-189734326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77427613	chr1:189734364-189734365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530762355	chr1:189739923-189739924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550451999	chr1:189739933-189739934	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs567183297	chr1:189739949-189739950	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs74138320	chr1:189739965-189739966	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs536680453	chr1:189739966-189739967	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546254199	chr1:189739984-189739985	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs184421694	chr1:189740108-189740109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs545128879	chr1:189740110-189740111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs12137159	chr1:189740122-189740123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs376128881	chr1:189740130-189740131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs559150842	chr1:189740148-189740149	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549931465	chr1:189743409-189743410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192326468	chr1:189743414-189743415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184877343	chr1:189743415-189743416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541587110	chr1:189743432-189743433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548993230	chr1:189743439-189743440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536612177	chr1:189743440-189743441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141797414	chr1:189743493-189743494	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
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
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189733200-189734200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr1:189733400-189734000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:189733400-189734000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr1:189733400-189734400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr1:189743400-189743600	Enhancers	A549	lung
6	chr1:189743600-189744800	Flanking Active TSS	A549	lung
7	chr1:189744000-189744600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:189744000-189745000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr1:189744000-189745200	Enhancers	Fetal Heart	heart
10	chr1:189744200-189745000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:189744200-189745000	Enhancers	NH-A	brain
12	chr1:189744400-189744800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:189744400-189745000	Enhancers	Hela-S3	cervix
14	chr1:189744800-189745000	Enhancers	A549	lung
15	chr1:189745000-189745200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:189745200-189746200	Weak transcription	Fetal Heart	heart
17	chr1:189746200-189746800	Enhancers	Fetal Heart	heart
18	chr1:189751000-189751800	Enhancers	Fetal Brain Male	brain
19	chr1:189751400-189751800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:189751800-189754800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:189754600-189755600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:189754800-189756200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:189755600-189756000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:189756000-189756200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:189756200-189756400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:189756200-189756600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:189756200-189756600	Active TSS	Fetal Brain Female	brain
28	chr1:189756400-189756600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:189756400-189756600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:189756400-189756800	Active TSS	Brain Substantia Nigra	brain
31	chr1:189756600-189757600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:189757200-189757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:189761800-189765400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:189773400-189773800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:189773400-189773800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:189773400-189773800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:189773400-189774000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:189773400-189774000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:189773400-189774000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:189773400-189774000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:189773400-189774000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:189773400-189774200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:189773600-189774000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:189774600-189775800	Enhancers	HUVEC	blood vessel
45	chr1:189774800-189775600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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