Variant report

Variant	esv2757735
Chromosome Location	chr1:73181612-73307170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 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	CEBPB	chr1:73292929-73293340	Hela-S3	cervix:	n/a	chr1:73293129-73293140
2	CEBPB	chr1:73293001-73293284	IMR90	lung:	n/a	chr1:73293129-73293140
3	CEBPB	chr1:73297208-73297267	K562	blood:	n/a	chr1:73297245-73297256
4	CEBPB	chr1:73297099-73297416	IMR90	lung:	n/a	chr1:73297245-73297256
5	CEBPB	chr1:73297099-73297422	HepG2	liver:	n/a	chr1:73297245-73297256
6	CEBPB	chr1:73292997-73293334	ECC-1	luminal epithelium:	n/a	chr1:73293129-73293140
7	CEBPB	chr1:73293075-73293311	H1-hESC	embryonic stem cell:	n/a	chr1:73293129-73293140
8	CEBPB	chr1:73292976-73293274	HepG2	liver:	n/a	chr1:73293129-73293140
9	CEBPB	chr1:73293036-73293299	ECC-1	luminal epithelium:	n/a	chr1:73293129-73293140
10	CHD2	chr1:73303597-73303601	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr1:73296304-73296502	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr1:73190680-73190830	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr1:73190660-73190810	HEK293	kidney:	n/a	n/a
14	CTCF	chr1:73186123-73186204	Medullo	brain:	n/a	n/a
15	CTCF	chr1:73190800-73190950	GM12874	blood:	n/a	n/a
16	CTCF	chr1:73190694-73190847	ProgFib	skin:	n/a	n/a
17	CTCF	chr1:73190640-73190790	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr1:73296814-73296915	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:73225540-73225690	HMEC	breast:	n/a	n/a
20	CTCF	chr1:73190620-73190770	HMEC	breast:	n/a	n/a
21	CTCF	chr1:73262861-73262927	Lung_OC	lung:	n/a	n/a
22	CTCF	chr1:73186183-73186242	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr1:73190652-73190819	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr1:73247408-73247458	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:73190744-73190829	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:73190639-73190881	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr1:73277327-73277402	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:73190694-73190795	LNCaP	prostate:	n/a	n/a
29	CTCF	chr1:73190743-73190806	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:73190660-73190810	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr1:73190669-73190834	Medullo	brain:	n/a	n/a
32	CTCF	chr1:73190640-73190790	NHEK	skin:	n/a	n/a
33	CTCF	chr1:73304243-73304247	GM13976	blood:	n/a	n/a
34	CTCF	chr1:73190720-73190870	GM12865	blood:	n/a	n/a
35	CTCF	chr1:73190680-73190830	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr1:73190731-73190805	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:73290040-73290190	HMEC	breast:	n/a	n/a
38	CTCF	chr1:73290092-73290373	GM12878	blood:	n/a	n/a
39	CTCF	chr1:73190660-73190810	Caco-2	colon:	n/a	n/a
40	CTCF	chr1:73290140-73290290	HMF	breast:	n/a	n/a
41	CTCF	chr1:73225540-73225690	HAc	cerebellar:	n/a	n/a
42	CTCF	chr1:73190727-73190816	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:73245920-73246070	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:73290060-73290210	HPF	lung:	n/a	n/a
45	CTCF	chr1:73190561-73191066	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr1:73290140-73290290	HMEC	breast:	n/a	n/a
47	CTCF	chr1:73190680-73190830	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr1:73290188-73290292	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr1:73296740-73296890	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr1:73190726-73190798	Hela-S3	cervix:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:73243724..73245872-chr1:73288517..73290287,2	MCF-7	breast:
2	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
3	chr1:73243724..73245872-chr1:73288517..73290287,2	MCF-7	breast:
4	chr1:73181346..73184286-chr1:73186090..73189025,2	K562	blood:
5	chr1:73185954..73186525-chr1:73310681..73311355,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-5	chr1:73245790-73245976	XLOC_000254
2	lnc-FPGT-5	chr1:73240954-73241227	XLOC_000254
3	lnc-FPGT-5	chr1:73240955-73241227	ENSG00000227016.2
4	lnc-FPGT-5	chr1:73243956-73244040	ENSG00000227016.2
5	lnc-FPGT-5	chr1:73243956-73244040	XLOC_000254
6	lnc-NEGR1-1	chr1:73214604-73214711	ENSG00000225087
7	lnc-FPGT-5	chr1:73249353-73249566	XLOC_000254
8	lnc-FPGT-5	chr1:73230714-73230763	ENSG00000227016.2
9	lnc-NEGR1-1	chr1:73214849-73214959	ENSG00000225087
10	lnc-FPGT-5	chr1:73245790-73245974	ENSG00000227016.2
11	lnc-FPGT-5	chr1:73252310-73252664	XLOC_000254
12	lnc-FPGT-5	chr1:73256748-73256963	XLOC_000254
13	lnc-FPGT-5	chr1:73243956-73244040	XLOC_000254
14	lnc-FPGT-5	chr1:73249353-73249663	XLOC_000254
15	lnc-FPGT-5	chr1:73240864-73241227	XLOC_000254

No data

Variant related genes	Relation type
ENSG00000227016	TF binding region
RNU6-1246P	TF binding region
ENSG00000212366	chromatin interactions
SERPINE1	miRNA target sites
SERP1	miRNA target sites

Extended variants
information (count: 1254 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1254 , 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	rs530853951	chr1:73183461-73183462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567817316	chr1:73184326-73184327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs148112717	chr1:73184370-73184371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs528077211	chr1:73184383-73184384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369309431	chr1:73184392-73184393	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs567903576	chr1:73184396-73184397	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536835811	chr1:73184419-73184420	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182645328	chr1:73184421-73184422	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377287419	chr1:73184501-73184502	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs570280454	chr1:73184542-73184543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs539095187	chr1:73184571-73184572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs6685349	chr1:73186096-73186097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs75412374	chr1:73186102-73186103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72948923	chr1:73186150-73186151	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs116387734	chr1:73186211-73186212	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192025843	chr1:73186225-73186226	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113650281	chr1:73186231-73186232	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566287402	chr1:73186243-73186244	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528541827	chr1:73186278-73186279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548670003	chr1:73186296-73186297	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568313714	chr1:73186320-73186321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537091616	chr1:73186338-73186339	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78038289	chr1:73186346-73186347	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556827470	chr1:73186394-73186395	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185265384	chr1:73186405-73186406	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539223877	chr1:73186414-73186415	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141957762	chr1:73186416-73186417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189677672	chr1:73186446-73186447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370275030	chr1:73186475-73186476	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs58027093	chr1:73186497-73186498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181323168	chr1:73186516-73186517	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144244748	chr1:73186558-73186559	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186728625	chr1:73186567-73186568	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544262062	chr1:73186712-73186713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563951769	chr1:73186772-73186773	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188145733	chr1:73186797-73186798	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs5775143	chr1:73186867-73186868	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34259142	chr1:73186877-73186878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs3980364	chr1:73186883-73186884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370755800	chr1:73186884-73186885	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376862926	chr1:73186893-73186894	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs202006014	chr1:73186920-73186921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374510609	chr1:73186949-73186950	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546533684	chr1:73186960-73186961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559647860	chr1:73186973-73186974	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371856143	chr1:73186974-73186975	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs180951254	chr1:73187011-73187012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs548388094	chr1:73187133-73187134	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115628323	chr1:73187205-73187206	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2255225	chr1:73187211-73187212	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73190800-73191000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:73190800-73191600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr1:73191000-73191200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
4	chr1:73191000-73191600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:73191000-73191600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:73191200-73191600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:73213000-73215000	Enhancers	Brain Germinal Matrix	brain
8	chr1:73225800-73226000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:73234800-73235600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:73236600-73237200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:73236600-73237400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr1:73236800-73237400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:73237200-73242400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:73240800-73241000	Enhancers	Aorta	Aorta
15	chr1:73242400-73243600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:73242800-73243000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:73243000-73243400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:73243400-73243800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr1:73243400-73243800	Active TSS	Aorta	Aorta
20	chr1:73267200-73267600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:73271200-73272000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:73282600-73283200	Enhancers	Ovary	ovary
23	chr1:73292800-73293200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:73292800-73293400	Enhancers	Hela-S3	cervix
25	chr1:73293200-73293600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:73295400-73296600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:73296000-73296600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:73296000-73296800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:73296000-73297000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr1:73296000-73297000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:73296200-73296800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:73296200-73296800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:73296200-73296800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:73296200-73297000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:73296200-73297000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:73296200-73297000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:73296400-73296800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:73296400-73297000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:73296600-73297000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:73296600-73297000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr1:73296800-73299800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:73297000-73302400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr1:73302400-73302800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
44	chr1:73303200-73304400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:73303400-73303800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:73303400-73304200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr1:73303400-73304200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr1:73303400-73304200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr1:73303400-73304400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:73303400-73304400	Enhancers	HUES64 Cell Line	embryonic stem cell

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