Variant report

Variant	nsv461939
Chromosome Location	chr1:72555489-72717743
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	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
5	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
6	BHLHE40	chr1:72563429-72563467	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
8	CEBPB	chr1:72707115-72707480	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:72707185-72707435	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:72707179-72707470	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
12	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:72568532-72568868	IMR90	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
15	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
19	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:72588279-72588474	HepG2	liver:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
21	CEBPB	chr1:72707115-72707489	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:72568547-72568841	A549	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
23	CEBPB	chr1:72568541-72568867	HepG2	liver:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
24	CEBPB	chr1:72568659-72568859	K562	blood:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
25	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:72707117-72707455	A549	lung:	n/a	n/a
28	CEBPB	chr1:72588186-72588499	IMR90	lung:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
29	CEBPB	chr1:72707157-72707388	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
31	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPD	chr1:72707177-72707369	HepG2	liver:	n/a	n/a
33	CTCF	chr1:72652500-72652650	HBMEC	blood vessel:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
34	CTCF	chr1:72652480-72652630	HUVEC	blood vessel:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
35	CTCF	chr1:72601061-72601162	K562	blood:	n/a	n/a
36	CTCF	chr1:72652480-72652630	HCPEpiC	choroid plexus:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
37	CTCF	chr1:72652460-72652610	GM12875	blood:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
38	CTCF	chr1:72592280-72592430	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:72602939-72603035	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr1:72606130-72606201	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:72652500-72652650	HPF	lung:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
42	CTCF	chr1:72652500-72652650	GM12869	blood:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
43	CTCF	chr1:72652500-72652650	WERI-Rb-1	eye:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
44	CTCF	chr1:72626800-72626950	HVMF	connective:	n/a	n/a
45	CTCF	chr1:72652496-72652619	SK-N-SH_RA	brain:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
46	CTCF	chr1:72652560-72652710	MCF-7	breast:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
47	CTCF	chr1:72652520-72652670	GM12872	blood:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
48	CTCF	chr1:72652460-72652610	HCM	heart:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
49	CTCF	chr1:72652520-72652670	HCPEpiC	choroid plexus:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609
50	CTCF	chr1:72652479-72652704	SK-N-SH_RA	brain:	n/a	chr1:72652586-72652604 chr1:72652591-72652599 chr1:72652588-72652609

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72566690-72566740	GM12892	blood:	n/a
2	chr1:72566690-72566740	GM12891	blood:	n/a
3	chr1:72566690-72566740	PrEC	prostate:	n/a
4	chr1:72566690-72566740	AG04450	lung:	fetal
5	chr1:72566690-72566740	A549	lung:	n/a
6	chr1:72566690-72566740	HCT-116	colon:	n/a
7	chr1:72566690-72566740	ovcar-3	ovarian:	n/a
8	chr1:72566690-72566740	ECC-1	luminal epithelium:	n/a
9	chr1:72566690-72566740	PANC-1	pancreas:	n/a
10	chr1:72566690-72566740	AG09319	gingival:	n/a
11	chr1:72566690-72566740	NT2-D1	testis:	n/a
12	chr1:72566690-72566740	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:72566690-72566740	HRE	kidney:	n/a
14	chr1:72566690-72566740	NHDF-neo	bronchial:	n/a
15	chr1:72566690-72566740	H1-hESC	embryonic stem cell:	embryo
16	chr1:72566690-72566740	Hepatocyte	liver:	n/a
17	chr1:72566690-72566740	K562	blood:	n/a
18	chr1:72566690-72566740	HCM	heart:	n/a
19	chr1:72566690-72566740	CMK	blood:	n/a
20	chr1:72566690-72566740	AoSMC	blood vessel:	n/a
21	chr1:72566690-72566740	AG09309	skin:	n/a
22	chr1:72566690-72566740	AG10803	skin:	n/a
23	chr1:72566690-72566740	HRPEpiC	eye:	n/a
24	chr1:72566690-72566740	NB4	blood:	n/a
25	chr1:72566690-72566740	NH-A	brain:	n/a
26	chr1:72566690-72566740	RPTEC	kidney:	n/a
27	chr1:72566690-72566740	SKMC	muscle:	n/a
28	chr1:72566690-72566740	GM12878	blood:	n/a
29	chr1:72566690-72566740	Caco-2	colon:	n/a
30	chr1:72566690-72566740	HCF	heart:	n/a
31	chr1:72566690-72566740	SK-N-MC	brain:	n/a
32	chr1:72566690-72566740	SK-N-SH_RA	brain:	n/a
33	chr1:72566690-72566740	HIPEpiC	eye:	n/a
34	chr1:72566690-72566740	PFSK-1	brain:	n/a
35	chr1:72566690-72566740	HL-60	blood:	n/a
36	chr1:72566690-72566740	SAEC	small airway:	n/a
37	chr1:72566690-72566740	SK-N-SH	brain:	n/a
38	chr1:72566690-72566740	LNCaP	prostate:	n/a
39	chr1:72566690-72566740	HRCEpiC	kidney:	n/a
40	chr1:72566690-72566740	T-47D	breast:	n/a
41	chr1:72566690-72566740	HAEpiC	amniotic membrane:	n/a
42	chr1:72566690-72566740	U87	brain:	n/a
43	chr1:72566690-72566740	AG04449	skin:	fetal
44	chr1:72566690-72566740	HMEC	breast:	n/a
45	chr1:72566690-72566740	HepG2	liver:	n/a
46	chr1:72566690-72566740	Jurkat	blood:	n/a
47	chr1:72566690-72566740	BJ	skin:	n/a
48	chr1:72566690-72566740	HNPCEpiC	eye:	n/a
49	chr1:72566690-72566740	HCPEpiC	choroid plexus:	n/a
50	chr1:72566690-72566740	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:

Variant related genes	Relation type
NEGR1	TF binding region
NEGR1	CpG island

Extended variants
information (count: 4764 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:4764 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571509840	chr1:72556403-72556404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534165119	chr1:72556405-72556406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555537741	chr1:72556406-72556407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146798394	chr1:72556420-72556421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547582187	chr1:72556457-72556458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574082803	chr1:72556485-72556486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141657656	chr1:72556593-72556594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184054540	chr1:72556599-72556600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150286986	chr1:72556601-72556602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189191287	chr1:72556603-72556604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36066239	chr1:72556625-72556626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs137910548	chr1:72556649-72556650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112367262	chr1:72556653-72556654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386632322	chr1:72556756-72556757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112094792	chr1:72556757-72556758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561039560	chr1:72556758-72556759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181552728	chr1:72556780-72556781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537794166	chr1:72558801-72558802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535940293	chr1:72558817-72558818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113015256	chr1:72558932-72558933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149996936	chr1:72558953-72558954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555972763	chr1:72558989-72558990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75810132	chr1:72563811-72563812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35359503	chr1:72563819-72563820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548098384	chr1:72563959-72563960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545623776	chr1:72563968-72563969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528188332	chr1:72563969-72563970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374412036	chr1:72563977-72563978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371378734	chr1:72563989-72563990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142258547	chr1:72564021-72564022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369246598	chr1:72564032-72564033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536949558	chr1:72564054-72564055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556878470	chr1:72564130-72564131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576724284	chr1:72564170-72564171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188722073	chr1:72564260-72564261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552537571	chr1:72564268-72564269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75749325	chr1:72564281-72564282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541884075	chr1:72564330-72564331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561329840	chr1:72564337-72564338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373420790	chr1:72564346-72564347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574933512	chr1:72564388-72564389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559419673	chr1:72564432-72564433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544018457	chr1:72564503-72564504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115710065	chr1:72564555-72564556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192799913	chr1:72564608-72564609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146296118	chr1:72564614-72564615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369276052	chr1:72564641-72564642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112651850	chr1:72564659-72564660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559663695	chr1:72564708-72564709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139737875	chr1:72564722-72564723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cancer	21272361	CNVD
Obesity	21131291	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72556400-72556800	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr1:72558800-72559000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:72563800-72564400	Enhancers	Colon Smooth Muscle	Colon
4	chr1:72564400-72566600	Weak transcription	Colon Smooth Muscle	Colon
5	chr1:72566400-72567400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:72566600-72566800	Enhancers	Colon Smooth Muscle	Colon
7	chr1:72570800-72571600	Enhancers	HUVEC	blood vessel
8	chr1:72571600-72576600	Weak transcription	HUVEC	blood vessel
9	chr1:72574400-72574800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:72575400-72576000	Enhancers	Fetal Lung	lung
11	chr1:72575600-72575800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:72575800-72580200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:72576600-72578000	Enhancers	HUVEC	blood vessel
14	chr1:72578000-72580400	Weak transcription	HUVEC	blood vessel
15	chr1:72580200-72581800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:72580400-72580800	Enhancers	HUVEC	blood vessel
17	chr1:72581000-72581200	Enhancers	Colon Smooth Muscle	Colon
18	chr1:72581000-72581400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:72581200-72581400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:72581200-72583000	Weak transcription	Colon Smooth Muscle	Colon
21	chr1:72581800-72586800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:72583000-72583800	Enhancers	HSMMtube	muscle
23	chr1:72583000-72584200	Enhancers	Colon Smooth Muscle	Colon
24	chr1:72583800-72585400	Weak transcription	HSMMtube	muscle
25	chr1:72584200-72586400	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:72584800-72585800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:72585400-72585800	Enhancers	HSMMtube	muscle
28	chr1:72585800-72587400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:72585800-72587600	Weak transcription	HSMMtube	muscle
30	chr1:72586400-72587000	Enhancers	Colon Smooth Muscle	Colon
31	chr1:72586800-72587200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:72587200-72587800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:72587200-72587800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:72587400-72588800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:72587600-72588000	Enhancers	Fetal Lung	lung
36	chr1:72587600-72588800	Enhancers	HSMMtube	muscle
37	chr1:72587600-72589200	Enhancers	NHDF-Ad	bronchial
38	chr1:72587800-72588200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:72587800-72588400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:72587800-72589200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:72588000-72588800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:72588000-72588800	Enhancers	HSMM	muscle
43	chr1:72588200-72588400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:72588400-72588600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:72588400-72589000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:72588600-72589000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:72588800-72591400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:72589000-72589200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:72589000-72591400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:72589200-72591200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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