Variant report

Variant	nsv1002973
Chromosome Location	chr1:104546037-104641567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:306)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 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	BACH1	chr1:104612948-104613054	K562	blood:	n/a	n/a
2	BCL11A	chr1:104635351-104635616	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr1:104635379-104635659	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:104562610-104562846	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:104562293-104562645	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr1:104585450-104585754	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:104562642-104562864	A549	lung:	n/a	n/a
8	CEBPB	chr1:104619494-104619671	IMR90	lung:	n/a	chr1:104619629-104619640
9	CEBPB	chr1:104607042-104607460	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:104562260-104562820	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr1:104562695-104562839	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:104627016-104627263	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:104619489-104619773	HepG2	liver:	n/a	chr1:104619629-104619640
14	CHD2	chr1:104635385-104635646	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:104625032-104625116	GM12878	blood:	n/a	n/a
16	CTCF	chr1:104562060-104562210	GM12878	blood:	n/a	n/a
17	CTCF	chr1:104561800-104561950	GM12869	blood:	n/a	n/a
18	CTCF	chr1:104562020-104562170	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:104562120-104562270	GM12875	blood:	n/a	n/a
20	CTCF	chr1:104562020-104562170	GM12872	blood:	n/a	n/a
21	CTCF	chr1:104561640-104561790	GM12864	blood:	n/a	n/a
22	CTCF	chr1:104562040-104562190	GM12872	blood:	n/a	n/a
23	CTCF	chr1:104561740-104561890	GM12866	blood:	n/a	n/a
24	CTCF	chr1:104562020-104562170	HEK293	kidney:	n/a	n/a
25	CTCF	chr1:104561620-104561770	GM12870	blood:	n/a	n/a
26	CTCF	chr1:104603860-104604010	GM12873	blood:	n/a	n/a
27	CTCF	chr1:104562060-104562210	BE2_C	brain:	n/a	n/a
28	CTCF	chr1:104562020-104562170	GM12869	blood:	n/a	n/a
29	CTCF	chr1:104562060-104562210	GM12866	blood:	n/a	n/a
30	CTCF	chr1:104561680-104561830	GM12870	blood:	n/a	n/a
31	CTCF	chr1:104561660-104561861	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:104561740-104561890	GM12864	blood:	n/a	n/a
33	CTCF	chr1:104599713-104599802	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr1:104561980-104562130	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:104562084-104562160	GM13977	blood:	n/a	n/a
36	CTCF	chr1:104561380-104561530	GM12864	blood:	n/a	n/a
37	CTCF	chr1:104562060-104562210	GM12873	blood:	n/a	n/a
38	CTCF	chr1:104561680-104561830	GM12865	blood:	n/a	n/a
39	CTCF	chr1:104625940-104626090	HCM	heart:	n/a	n/a
40	CTCF	chr1:104561980-104562130	GM12870	blood:	n/a	n/a
41	CTCF	chr1:104600080-104600230	HepG2	liver:	n/a	n/a
42	CTCF	chr1:104561640-104561790	GM12874	blood:	n/a	n/a
43	CTCF	chr1:104561640-104561790	GM12867	blood:	n/a	n/a
44	CTCF	chr1:104624911-104625223	GM12878	blood:	n/a	n/a
45	CTCF	chr1:104562160-104562310	GM12870	blood:	n/a	n/a
46	CTCF	chr1:104607130-104607138	GM13977	blood:	n/a	n/a
47	CTCF	chr1:104561720-104561870	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:104561680-104561830	BE2_C	brain:	n/a	n/a
49	CTCF	chr1:104562060-104562210	GM12874	blood:	n/a	n/a
50	CTCF	chr1:104561680-104561830	GM12872	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104616118-104616168	NH-A	brain:	n/a
2	chr1:104616118-104616168	NH-A	brain:	n/a
3	chr1:104616267-104616317	Hela-S3	cervix:	n/a
4	chr1:104616267-104616317	A549	lung:	n/a
5	chr1:104615609-104615659	ECC-1	luminal epithelium:	n/a
6	chr1:104616267-104616317	HUVEC	blood vessel:	n/a
7	chr1:104635600-104635650	AG04450	lung:	fetal
8	chr1:104615609-104615659	BE2_C	brain:	n/a
9	chr1:104615609-104615659	U87	brain:	n/a
10	chr1:104616267-104616317	AG04449	skin:	fetal
11	chr1:104615867-104615917	GM19239	blood:	n/a
12	chr1:104615867-104615917	BE2_C	brain:	n/a
13	chr1:104616118-104616168	SK-N-SH_RA	brain:	n/a
14	chr1:104615867-104615917	AG09309	skin:	n/a
15	chr1:104616267-104616317	HRPEpiC	eye:	n/a
16	chr1:104615609-104615659	GM06990	blood:	n/a
17	chr1:104635600-104635650	HCT-116	colon:	n/a
18	chr1:104615609-104615659	HNPCEpiC	eye:	n/a
19	chr1:104615867-104615917	HRPEpiC	eye:	n/a
20	chr1:104615609-104615659	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:104616267-104616317	HNPCEpiC	eye:	n/a
22	chr1:104615867-104615917	SKMC	muscle:	n/a
23	chr1:104616118-104616168	SKMC	muscle:	n/a
24	chr1:104616267-104616317	AG09319	gingival:	n/a
25	chr1:104616118-104616168	Caco-2	colon:	n/a
26	chr1:104635600-104635650	ProgFib	skin:	n/a
27	chr1:104616267-104616317	GM12892	blood:	n/a
28	chr1:104616267-104616317	ECC-1	luminal epithelium:	n/a
29	chr1:104616118-104616168	NHBE	bronchial:	n/a
30	chr1:104616267-104616317	HAEpiC	amniotic membrane:	n/a
31	chr1:104635600-104635650	SK-N-SH	brain:	n/a
32	chr1:104616118-104616168	SK-N-MC	brain:	n/a
33	chr1:104615609-104615659	HIPEpiC	eye:	n/a
34	chr1:104635600-104635650	IMR90	lung:	fetal
35	chr1:104635600-104635650	Caco-2	colon:	n/a
36	chr1:104616118-104616168	AG04450	lung:	fetal
37	chr1:104616118-104616168	ProgFib	skin:	n/a
38	chr1:104615867-104615917	HepG2	liver:	n/a
39	chr1:104615609-104615659	HCM	heart:	n/a
40	chr1:104616118-104616168	IMR90	lung:	fetal
41	chr1:104635600-104635650	Hela-S3	cervix:	n/a
42	chr1:104616267-104616317	HRE	kidney:	n/a
43	chr1:104616118-104616168	GM06990	blood:	n/a
44	chr1:104635600-104635650	GM12878	blood:	n/a
45	chr1:104616118-104616168	HCPEpiC	choroid plexus:	n/a
46	chr1:104616118-104616168	HAEpiC	amniotic membrane:	n/a
47	chr1:104615867-104615917	PANC-1	pancreas:	n/a
48	chr1:104615609-104615659	HMEC	breast:	n/a
49	chr1:104615609-104615659	T-47D	breast:	n/a
50	chr1:104615867-104615917	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:
2	chr1:104569816..104571688-chr1:104580408..104582171,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000243500	TF binding region
ENSG00000215869	TF binding region
ENSG00000243500	CpG island
ENSG00000215869	CpG island

Extended variants
information (count: 895 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534358992	chr1:104566002-104566003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553390140	chr1:104566038-104566039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536804066	chr1:104566081-104566082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372817089	chr1:104566269-104566270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553725899	chr1:104566272-104566273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78836026	chr1:104566314-104566315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376647913	chr1:104566324-104566325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78427497	chr1:104566336-104566337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201539782	chr1:104566342-104566343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147375497	chr1:104566411-104566412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139288879	chr1:104566478-104566479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569332418	chr1:104566496-104566497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540586653	chr1:104566512-104566513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115525938	chr1:104566520-104566521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1980690	chr1:104566523-104566524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141511719	chr1:104566547-104566548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150914722	chr1:104566548-104566549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569812478	chr1:104566551-104566552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530652744	chr1:104566589-104566590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370513225	chr1:104570841-104570842	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs200505034	chr1:104570902-104570903	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs529180928	chr1:104570923-104570924	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs12025999	chr1:104570934-104570935	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs5006566	chr1:104570982-104570983	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12026039	chr1:104571091-104571092	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs544246560	chr1:104571101-104571102	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs557463736	chr1:104571119-104571120	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs562920098	chr1:104571150-104571151	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs569299658	chr1:104571156-104571157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs536695902	chr1:104571168-104571169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs368655207	chr1:104571173-104571174	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs573955340	chr1:104571232-104571233	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs191141928	chr1:104571250-104571251	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs542492235	chr1:104571385-104571386	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs578132624	chr1:104571507-104571508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545471387	chr1:104571509-104571510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563815932	chr1:104571519-104571520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12031339	chr1:104571543-104571544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543000721	chr1:104571581-104571582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561281137	chr1:104571602-104571603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183288745	chr1:104571612-104571613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187510949	chr1:104571637-104571638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137975472	chr1:104571677-104571678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533019801	chr1:104571700-104571701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12030485	chr1:104571720-104571721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113252412	chr1:104571781-104571782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551057915	chr1:104571789-104571790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191349015	chr1:104571805-104571806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59789357	chr1:104571822-104571823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs375060241	chr1:104571882-104571883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104566000-104566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:104570800-104571400	Active TSS	Fetal Lung	lung
3	chr1:104571400-104572200	Weak transcription	Fetal Lung	lung
4	chr1:104572200-104573600	Enhancers	Fetal Lung	lung
5	chr1:104573200-104573600	Enhancers	Fetal Heart	heart
6	chr1:104594600-104595000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:104595200-104599400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:104599200-104600800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:104599400-104600000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr1:104599400-104600000	Active TSS	HepG2	liver
11	chr1:104599400-104600400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:104599400-104600400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr1:104599400-104600400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:104599400-104600600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:104599400-104600800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:104599600-104600000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:104599600-104600600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:104599600-104600600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:104599600-104600600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:104599600-104600600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:104599600-104600600	Enhancers	Colonic Mucosa	Colon
22	chr1:104599600-104600800	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr1:104600000-104600400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:104600000-104600400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:104600200-104600600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:104615600-104616200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:104615600-104616400	Active TSS	Pancreas	Pancrea
28	chr1:104615600-104616400	Active TSS	Right Ventricle	heart
29	chr1:104615600-104616600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:104615600-104616600	Active TSS	Fetal Stomach	stomach
31	chr1:104626000-104627000	Enhancers	Fetal Heart	heart
32	chr1:104626200-104626600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:104626200-104626600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
34	chr1:104626600-104627400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:104626600-104627600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:104626800-104627200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr1:104626800-104627600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:104626800-104627600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr1:104626800-104627600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:104626800-104627600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:104626800-104627600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:104626800-104627600	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr1:104626800-104628400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:104626800-104629000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr1:104627400-104627800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:104627600-104634600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr1:104627600-104634600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:104627800-104628000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:104628000-104634600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:104628400-104634600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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