Variant report

Variant	nsv548650
Chromosome Location	chr1:192246590-192324175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:192246884-192247112	K562	blood:	n/a	n/a
2	ARID3A	chr1:192280293-192280660	K562	blood:	n/a	n/a
3	ATF1	chr1:192272985-192273118	K562	blood:	n/a	n/a
4	ATF1	chr1:192275036-192275081	K562	blood:	n/a	n/a
5	BACH1	chr1:192285827-192285912	K562	blood:	n/a	n/a
6	BRCA1	chr1:192254302-192254344	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr1:192277478-192277742	K562	blood:	n/a	n/a
8	CBX3	chr1:192250251-192250667	K562	blood:	n/a	n/a
9	CBX3	chr1:192277415-192277815	K562	blood:	n/a	n/a
10	CEBPB	chr1:192295560-192295826	K562	blood:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
11	CEBPB	chr1:192294118-192294318	HepG2	liver:	n/a	chr1:192294239-192294250
12	CEBPB	chr1:192278595-192278597	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:192305030-192305200	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:192289480-192289498	HepG2	liver:	n/a	chr1:192289481-192289492
15	CEBPB	chr1:192295571-192295831	HepG2	liver:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
16	CEBPB	chr1:192266856-192267080	HepG2	liver:	n/a	chr1:192266996-192267007
17	CEBPB	chr1:192281351-192281484	A549	lung:	n/a	n/a
18	CEBPB	chr1:192299264-192299313	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:192266819-192267127	K562	blood:	n/a	chr1:192266996-192267007
20	CEBPZ	chr1:192257435-192257475	HepG2	liver:	n/a	n/a
21	CTCF	chr1:192280540-192280690	HUVEC	blood vessel:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
22	CTCF	chr1:192280460-192280610	RPTEC	kidney:	n/a	n/a
23	CTCF	chr1:192280480-192280630	GM06990	blood:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
24	CTCF	chr1:192280540-192280690	HFF-Myc	foreskin:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
25	CTCF	chr1:192280520-192280670	GM12872	blood:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
26	CTCF	chr1:192280540-192280690	AG10803	skin:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
27	CTCF	chr1:192280516-192280707	Gliobla	brain:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
28	CTCF	chr1:192280509-192280717	SK-N-SH_RA	brain:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
29	CTCF	chr1:192280526-192280726	Pancreas_OC	pancreas:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
30	CTCF	chr1:192280520-192280670	HCT-116	colon:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
31	CTCF	chr1:192277926-192277992	GM10248	blood:	n/a	n/a
32	CTCF	chr1:192280540-192280690	HBMEC	blood vessel:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
33	CTCF	chr1:192280564-192280694	GM13977	blood:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
34	CTCF	chr1:192280580-192280730	HEEpiC	esophagus:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
35	CTCF	chr1:192280504-192280714	Spleen_OC	spleen:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
36	CTCF	chr1:192280640-192280790	HVMF	connective:	n/a	n/a
37	CTCF	chr1:192280520-192280670	HPF	lung:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
38	CTCF	chr1:192280540-192280690	AG04450	lung:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
39	CTCF	chr1:192280260-192280928	A549	lung:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
40	CTCF	chr1:192280540-192280690	HCPEpiC	choroid plexus:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
41	CTCF	chr1:192280540-192280690	HPAF	blood vessel:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
42	CTCF	chr1:192280640-192280790	NHLF	lung:	n/a	n/a
43	CTCF	chr1:192280540-192280690	HCT-116	colon:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
44	CTCF	chr1:192280455-192280724	K562	blood:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
45	CTCF	chr1:192280500-192280650	GM12871	blood:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
46	CTCF	chr1:192280500-192280650	HUVEC	blood vessel:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
47	CTCF	chr1:192280460-192280610	HAc	cerebellar:	n/a	n/a
48	CTCF	chr1:192280520-192280670	AG04450	lung:	n/a	chr1:192280604-192280625 chr1:192280609-192280627
49	CTCF	chr1:192251302-192251373	GM12878	blood:	n/a	n/a
50	CTCF	chr1:192280560-192280710	HA-sp	spinal cord:	n/a	chr1:192280604-192280625 chr1:192280609-192280627

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:192304785-192304835	Hepatocyte	liver:	n/a
2	chr1:192285333-192285383	HEEpiC	esophagus:	n/a
3	chr1:192304785-192304835	HCF	heart:	n/a
4	chr1:192304785-192304835	HCT-116	colon:	n/a
5	chr1:192285333-192285383	NHBE	bronchial:	n/a
6	chr1:192285333-192285383	PrEC	prostate:	n/a
7	chr1:192304785-192304835	HCM	heart:	n/a
8	chr1:192285333-192285383	H1-hESC	embryonic stem cell:	embryo
9	chr1:192304785-192304835	U87	brain:	n/a
10	chr1:192285333-192285383	HCM	heart:	n/a
11	chr1:192304785-192304835	NHBE	bronchial:	n/a
12	chr1:192304785-192304835	LNCaP	prostate:	n/a
13	chr1:192304785-192304835	AG10803	skin:	n/a
14	chr1:192304785-192304835	SK-N-SH	brain:	n/a
15	chr1:192285333-192285383	PANC-1	pancreas:	n/a
16	chr1:192285333-192285383	HRCEpiC	kidney:	n/a
17	chr1:192285333-192285383	AG09319	gingival:	n/a
18	chr1:192285333-192285383	HCT-116	colon:	n/a
19	chr1:192304785-192304835	SK-N-SH_RA	brain:	n/a
20	chr1:192285333-192285383	HIPEpiC	eye:	n/a
21	chr1:192285333-192285383	HL-60	blood:	n/a
22	chr1:192304785-192304835	GM12892	blood:	n/a
23	chr1:192304785-192304835	HRCEpiC	kidney:	n/a
24	chr1:192304785-192304835	IMR90	lung:	fetal
25	chr1:192285333-192285383	NHDF-neo	bronchial:	n/a
26	chr1:192285333-192285383	GM12891	blood:	n/a
27	chr1:192285333-192285383	SK-N-MC	brain:	n/a
28	chr1:192304785-192304835	HEEpiC	esophagus:	n/a
29	chr1:192285333-192285383	SK-N-SH_RA	brain:	n/a
30	chr1:192304785-192304835	NT2-D1	testis:	n/a
31	chr1:192304785-192304835	NHDF-neo	bronchial:	n/a
32	chr1:192285333-192285383	MCF10A-Er-Src	breast:	n/a
33	chr1:192285333-192285383	NT2-D1	testis:	n/a
34	chr1:192285333-192285383	NH-A	brain:	n/a
35	chr1:192285333-192285383	AoSMC	blood vessel:	n/a
36	chr1:192304785-192304835	GM06990	blood:	n/a
37	chr1:192304785-192304835	K562	blood:	n/a
38	chr1:192304785-192304835	HL-60	blood:	n/a
39	chr1:192304785-192304835	HRE	kidney:	n/a
40	chr1:192304785-192304835	AG09319	gingival:	n/a
41	chr1:192304785-192304835	T-47D	breast:	n/a
42	chr1:192285333-192285383	BJ	skin:	n/a
43	chr1:192304785-192304835	HNPCEpiC	eye:	n/a
44	chr1:192285333-192285383	PFSK-1	brain:	n/a
45	chr1:192304785-192304835	A549	lung:	n/a
46	chr1:192285333-192285383	AG04450	lung:	fetal
47	chr1:192285333-192285383	LNCaP	prostate:	n/a
48	chr1:192304785-192304835	GM12891	blood:	n/a
49	chr1:192285333-192285383	Hela-S3	cervix:	n/a
50	chr1:192285333-192285383	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
2	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
3	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:
4	chr1:192238542..192241818-chr1:192250028..192252934,3	K562	blood:
5	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
6	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
7	chr1:192242181..192244363-chr1:192263112..192265270,2	K562	blood:
8	chr1:191962409..191963306-chr1:192269925..192270965,3	MCF-7	breast:
9	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
10	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
11	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
12	chr1:192234066..192236164-chr1:192244600..192247164,2	K562	blood:
13	chr1:192249186..192250692-chr1:192255900..192258274,2	K562	blood:
14	chr1:191962436..191963394-chr1:192279940..192280907,5	MCF-7	breast:
15	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:
16	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
17	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
18	chr1:192249186..192250692-chr1:192255900..192258274,2	K562	blood:
19	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
20	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
21	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
22	chr1:192312588..192314663-chr1:192330429..192332047,2	K562	blood:

Variant related genes	Relation type
RGS21	TF binding region
RGS21	CpG island

Extended variants
information (count: 1015 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1175121	chr1:192246590-192246591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191599668	chr1:192246616-192246617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182485365	chr1:192246658-192246659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185316995	chr1:192246706-192246707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78529098	chr1:192246761-192246762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74264612	chr1:192246770-192246771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76710637	chr1:192246771-192246772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77516466	chr1:192246773-192246774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562944562	chr1:192246800-192246801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1175120	chr1:192246847-192246848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529686474	chr1:192246911-192246912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562246149	chr1:192246985-192246986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182791104	chr1:192247033-192247034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139409833	chr1:192247063-192247064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76406066	chr1:192247087-192247088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187826438	chr1:192247090-192247091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560276854	chr1:192247149-192247150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148758883	chr1:192247150-192247151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182965853	chr1:192247188-192247189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187586722	chr1:192247208-192247209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548796705	chr1:192247280-192247281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112808267	chr1:192247304-192247305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565855675	chr1:192247354-192247355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192994599	chr1:192247381-192247382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547876052	chr1:192247411-192247412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570818990	chr1:192247469-192247470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539839027	chr1:192247508-192247509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548187241	chr1:192247533-192247534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146415164	chr1:192247573-192247574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375136214	chr1:192247574-192247575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184186828	chr1:192247613-192247614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576836911	chr1:192247616-192247617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368209954	chr1:192247693-192247694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536141458	chr1:192247696-192247697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12743592	chr1:192247764-192247765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569800623	chr1:192247784-192247785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187063104	chr1:192247807-192247808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541225928	chr1:192247884-192247885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147738279	chr1:192247963-192247964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6428092	chr1:192260413-192260414	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs113269255	chr1:192260473-192260474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375558063	chr1:192260478-192260479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560244278	chr1:192260534-192260535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541798370	chr1:192260611-192260612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540585978	chr1:192260631-192260632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77591859	chr1:192260668-192260669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545514965	chr1:192260719-192260720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146153174	chr1:192260745-192260746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527527463	chr1:192260749-192260750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527630255	chr1:192260791-192260792	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192246400-192247000	Weak transcription	K562	blood
2	chr1:192247000-192248000	Enhancers	K562	blood
3	chr1:192260400-192260800	Enhancers	HUVEC	blood vessel
4	chr1:192272200-192273000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:192273000-192276400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:192276400-192276800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:192280200-192280800	Enhancers	Dnd41	blood
8	chr1:192283200-192283600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:192283600-192286000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:192286000-192286600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:192291200-192292000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr1:192291600-192292200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr1:192292200-192292400	Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr1:192292400-192292600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr1:192298800-192299400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:192298800-192299600	Enhancers	Fetal Intestine Large	intestine
17	chr1:192299400-192299600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:192299600-192299800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:192303600-192307000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:192303800-192306800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:192304000-192306000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr1:192304000-192308000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:192304600-192305800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:192305800-192307200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:192306000-192312200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:192307200-192307800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:192307800-192312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:192308000-192312200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:192311200-192312800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:192311800-192312000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:192312000-192312600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr1:192312000-192312800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:192312000-192313000	Enhancers	HSMM	muscle
34	chr1:192312200-192312800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:192312200-192312800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:192312200-192312800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:192312200-192312800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr1:192312200-192313000	Enhancers	HSMMtube	muscle
39	chr1:192312400-192312800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:192312600-192312800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:192312600-192313000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:192312800-192318200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:192318200-192318600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:192318200-192319000	Enhancers	Fetal Lung	lung
45	chr1:192318400-192318800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:192319000-192319400	Weak transcription	Fetal Lung	lung
47	chr1:192319400-192319800	Enhancers	Fetal Lung	lung
48	chr1:192319600-192320000	Enhancers	Fetal Intestine Large	intestine
49	chr1:192319600-192320000	Enhancers	Fetal Muscle Leg	muscle

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