Variant report

Variant	nsv873137
Chromosome Location	chr1:209301571-209338673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:159)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:159 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:209323481-209323798	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr1:209323543-209323838	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr1:209323572-209323859	A549	lung:	n/a	n/a
4	CEBPB	chr1:209323540-209323834	MCF-7	breast:	n/a	n/a
5	CEBPB	chr1:209323533-209323840	A549	lung:	n/a	n/a
6	CEBPB	chr1:209323500-209323852	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:209323541-209323906	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:209323521-209323856	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:209317730-209317828	IMR90	lung:	n/a	chr1:209317763-209317774 chr1:209317762-209317773
10	CEBPB	chr1:209317629-209317879	HepG2	liver:	n/a	chr1:209317763-209317774 chr1:209317762-209317773
11	CEBPB	chr1:209323504-209323790	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:209323501-209323862	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr1:209330667-209330727	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr1:209323537-209323552	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:209311631-209311676	ProgFib	skin:	n/a	n/a
16	CTCF	chr1:209333452-209333537	LNCaP	prostate:	n/a	n/a
17	CTCF	chr1:209323580-209323730	GM12864	blood:	n/a	n/a
18	CTCF	chr1:209336660-209336810	GM12865	blood:	n/a	n/a
19	CTCF	chr1:209305763-209305794	Medullo	brain:	n/a	n/a
20	CTCF	chr1:209337571-209337623	GM10248	blood:	n/a	n/a
21	CTCF	chr1:209322040-209322190	Caco-2	colon:	n/a	n/a
22	E2F4	chr1:209310325-209310355	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr1:209323510-209323782	MCF10A-Er-Src	breast:	n/a	chr1:209323618-209323625 chr1:209323618-209323625 chr1:209323618-209323625 chr1:209323731-209323740
24	E2F6	chr1:209316713-209317101	H1-hESC	embryonic stem cell:	n/a	n/a
25	E2F6	chr1:209316746-209317002	H1-hESC	embryonic stem cell:	n/a	n/a
26	EBF1	chr1:209307358-209307600	GM12878	blood:	n/a	n/a
27	EP300	chr1:209326667-209327375	SK-N-SH	brain:	n/a	chr1:209327229-209327243 chr1:209327201-209327214 chr1:209326958-209326967
28	EP300	chr1:209335964-209336520	SK-N-SH	brain:	n/a	n/a
29	EP300	chr1:209326783-209327168	SK-N-SH_RA	brain:	n/a	chr1:209326958-209326967
30	EP300	chr1:209326821-209327158	SK-N-SH_RA	brain:	n/a	chr1:209326958-209326967
31	FOS	chr1:209319221-209319370	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:209323628-209323778	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:209323613-209323727	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:209323573-209323812	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:209323613-209323811	MCF10A-Er-Src	breast:	n/a	n/a
36	FOSL2	chr1:209327280-209327623	SK-N-SH	brain:	n/a	n/a
37	FOSL2	chr1:209335947-209336386	SK-N-SH	brain:	n/a	n/a
38	FOXA1	chr1:209323574-209323756	T-47D	breast:	n/a	n/a
39	FOXA2	chr1:209314581-209314998	A549	lung:	n/a	n/a
40	GATA2	chr1:209303178-209303415	K562	blood:	n/a	n/a
41	GATA2	chr1:209320903-209320906	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr1:209320900-209321135	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr1:209319839-209319889	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr1:209316487-209316517	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr1:209317174-209317198	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr1:209335882-209336670	SK-N-SH	brain:	n/a	n/a
47	GATA3	chr1:209326634-209327693	SK-N-SH	brain:	n/a	chr1:209327103-209327110 chr1:209327096-209327117 chr1:209327103-209327110 chr1:209327101-209327111 chr1:209327092-209327109 chr1:209326731-209326741 chr1:209327103-209327110 chr1:209327101-209327110 chr1:209326957-209326966
48	GATA3	chr1:209326767-209327728	SK-N-SH	brain:	n/a	chr1:209327103-209327110 chr1:209327096-209327117 chr1:209327103-209327110 chr1:209327101-209327111 chr1:209327092-209327109 chr1:209327103-209327110 chr1:209327101-209327110 chr1:209326957-209326966
49	GATA3	chr1:209335925-209336562	SK-N-SH	brain:	n/a	n/a
50	GTF2F1	chr1:209329030-209329149	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:209304435-209304485	HCM	heart:	n/a
2	chr1:209304435-209304485	CMK	blood:	n/a
3	chr1:209304435-209304485	NH-A	brain:	n/a
4	chr1:209304435-209304485	HRE	kidney:	n/a
5	chr1:209304435-209304485	HCPEpiC	choroid plexus:	n/a
6	chr1:209304435-209304485	AG09319	gingival:	n/a
7	chr1:209304435-209304485	HRCEpiC	kidney:	n/a
8	chr1:209304435-209304485	AG04449	skin:	fetal
9	chr1:209304435-209304485	GM06990	blood:	n/a
10	chr1:209304435-209304485	NHBE	bronchial:	n/a
11	chr1:209304435-209304485	T-47D	breast:	n/a
12	chr1:209304435-209304485	PANC-1	pancreas:	n/a
13	chr1:209304435-209304485	BE2_C	brain:	n/a
14	chr1:209304435-209304485	SK-N-SH	brain:	n/a
15	chr1:209304435-209304485	PFSK-1	brain:	n/a
16	chr1:209304435-209304485	SAEC	small airway:	n/a
17	chr1:209304435-209304485	GM12878	blood:	n/a
18	chr1:209304435-209304485	HEK293	kidney:	embryo
19	chr1:209304435-209304485	Jurkat	blood:	n/a
20	chr1:209304435-209304485	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:209304435-209304485	A549	lung:	n/a
22	chr1:209304435-209304485	HAEpiC	amniotic membrane:	n/a
23	chr1:209304435-209304485	H1-hESC	embryonic stem cell:	embryo
24	chr1:209304435-209304485	RPTEC	kidney:	n/a
25	chr1:209304435-209304485	AG10803	skin:	n/a
26	chr1:209304435-209304485	MCF10A-Er-Src	breast:	n/a
27	chr1:209304435-209304485	NHDF-neo	bronchial:	n/a
28	chr1:209304435-209304485	K562	blood:	n/a
29	chr1:209304435-209304485	SKMC	muscle:	n/a
30	chr1:209304435-209304485	IMR90	lung:	fetal
31	chr1:209304435-209304485	GM12892	blood:	n/a
32	chr1:209304435-209304485	ovcar-3	ovarian:	n/a
33	chr1:209304435-209304485	HMEC	breast:	n/a
34	chr1:209304435-209304485	GM19239	blood:	n/a
35	chr1:209304435-209304485	HepG2	liver:	n/a
36	chr1:209304435-209304485	SK-N-SH_RA	brain:	n/a
37	chr1:209304435-209304485	NT2-D1	testis:	n/a
38	chr1:209304435-209304485	Hepatocyte	liver:	n/a
39	chr1:209304435-209304485	ProgFib	skin:	n/a
40	chr1:209304435-209304485	HL-60	blood:	n/a
41	chr1:209304435-209304485	LNCaP	prostate:	n/a
42	chr1:209304435-209304485	BJ	skin:	n/a
43	chr1:209304435-209304485	AoSMC	blood vessel:	n/a
44	chr1:209304435-209304485	AG04450	lung:	fetal
45	chr1:209304435-209304485	HIPEpiC	eye:	n/a
46	chr1:209304435-209304485	HNPCEpiC	eye:	n/a
47	chr1:209304435-209304485	U87	brain:	n/a
48	chr1:209304435-209304485	HRPEpiC	eye:	n/a
49	chr1:209304435-209304485	HCT-116	colon:	n/a
50	chr1:209304435-209304485	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:209299833..209301644-chr1:209317331..209320177,2	K562	blood:
2	chr1:209299833..209301644-chr1:209317331..209320177,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMB3-5	chr1:209332829-209332907	NONHSAT009183
2	lnc-LAMB3-3	chr1:209320612-209320939	ENSG00000232537
3	lnc-LAMB3-3	chr1:209328403-209328446	ENSG00000232537
4	lnc-LAMB3-3	chr1:209320650-209320939	NONHSAT009182
5	lnc-LAMB3-5	chr1:209328948-209329241	NONHSAT009183
6	lnc-LAMB3-3	chr1:209324750-209324854	NONHSAT009182
7	lnc-LAMB3-3	chr1:209324750-209324850	ENSG00000232537
8	lnc-LAMB3-5	chr1:209335060-209335176	NONHSAT009183

No data

Variant related genes	Relation type
ENSG00000232537	TF binding region
ENSG00000232537	CpG island

Extended variants
information (count: 1287 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6661599	chr1:209301571-209301572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557883849	chr1:209301574-209301575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571765899	chr1:209301578-209301579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141751980	chr1:209301659-209301660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150471509	chr1:209301689-209301690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189212519	chr1:209301698-209301699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557473964	chr1:209301709-209301710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567682558	chr1:209301710-209301711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181058084	chr1:209301712-209301713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549314649	chr1:209301720-209301721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113802994	chr1:209301747-209301748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71798482	chr1:209301783-209301784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544016316	chr1:209301788-209301789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143569813	chr1:209301804-209301805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565959475	chr1:209301812-209301813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539295474	chr1:209301850-209301851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373771568	chr1:209301869-209301870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557893126	chr1:209301870-209301871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570054568	chr1:209301899-209301900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537513770	chr1:209301946-209301947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377733126	chr1:209301975-209301976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541416073	chr1:209301979-209301980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553437098	chr1:209301994-209301995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6664753	chr1:209302003-209302004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11119228	chr1:209302021-209302022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12732751	chr1:209302077-209302078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563861188	chr1:209302083-209302084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377520460	chr1:209302084-209302085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538432455	chr1:209302094-209302095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543145914	chr1:209302100-209302101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561421021	chr1:209302162-209302163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528899492	chr1:209302163-209302164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143251958	chr1:209302164-209302165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184756106	chr1:209302179-209302180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539085926	chr1:209302248-209302249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111820804	chr1:209302265-209302266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188793955	chr1:209302333-209302334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370835179	chr1:209302347-209302348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200575104	chr1:209302352-209302353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549527293	chr1:209302436-209302437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567760590	chr1:209302473-209302474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113006119	chr1:209302477-209302478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535061831	chr1:209302479-209302480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201352199	chr1:209302480-209302481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562096346	chr1:209302505-209302506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553292573	chr1:209302541-209302542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578192371	chr1:209302544-209302545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539293975	chr1:209302552-209302553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557352401	chr1:209302556-209302557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575457648	chr1:209302557-209302558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
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
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
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	20406844	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209297000-209306200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:209298800-209307200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:209303600-209304200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr1:209303600-209304400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr1:209303600-209305800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:209303800-209304200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr1:209304000-209305000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr1:209304000-209305400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:209304000-209305800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:209304000-209306800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr1:209304200-209304400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr1:209304200-209305000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:209304400-209304600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:209304400-209304800	Active TSS	iPS-18 Cell Line	embryonic stem cell
15	chr1:209304600-209305200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
16	chr1:209304800-209305000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:209304800-209305200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr1:209305000-209305200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr1:209305000-209305200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:209305000-209307200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:209305200-209306000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:209305200-209306000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:209305200-209306400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:209305200-209306400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:209305400-209305800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:209305400-209306200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:209305800-209306600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:209305800-209306800	Enhancers	Fetal Muscle Trunk	muscle
29	chr1:209305800-209306800	Enhancers	Fetal Muscle Leg	muscle
30	chr1:209305800-209307200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:209306000-209306200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:209306000-209307600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:209306200-209306600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:209306200-209306800	Enhancers	Fetal Stomach	stomach
35	chr1:209306200-209307200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr1:209306400-209306600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr1:209306400-209306600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr1:209306400-209308400	Enhancers	GM12878-XiMat	blood
39	chr1:209306800-209307600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr1:209307200-209307600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:209307200-209307800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr1:209307200-209307800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:209307200-209308200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:209307400-209307600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:209307600-209307800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr1:209307600-209307800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr1:209307600-209308200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:209313400-209313600	Enhancers	Esophagus	oesophagus
49	chr1:209314200-209314600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr1:209314600-209316000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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