Variant report

Variant	nsv1013250
Chromosome Location	chr1:72603540-72762582
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	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
5	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
6	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
7	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
8	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
11	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
16	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:72707185-72707435	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:72707157-72707388	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
23	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:72707179-72707470	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
26	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:72707115-72707480	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:72731623-72731775	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:72707117-72707455	A549	lung:	n/a	n/a
33	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
34	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
35	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
36	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:72707115-72707489	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
40	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
41	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:72731625-72731886	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
47	CEBPD	chr1:72707177-72707369	HepG2	liver:	n/a	n/a
48	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72749581-72749631	HEEpiC	esophagus:	n/a
2	chr1:72749581-72749631	HEEpiC	esophagus:	n/a
3	chr1:72753076-72753126	NH-A	brain:	n/a
4	chr1:72748607-72748657	T-47D	breast:	n/a
5	chr1:72748389-72748439	HEEpiC	esophagus:	n/a
6	chr1:72749064-72749114	GM19239	blood:	n/a
7	chr1:72750241-72750291	PFSK-1	brain:	n/a
8	chr1:72748124-72748174	HCPEpiC	choroid plexus:	n/a
9	chr1:72749275-72749325	HNPCEpiC	eye:	n/a
10	chr1:72748389-72748439	SK-N-MC	brain:	n/a
11	chr1:72748389-72748439	HCM	heart:	n/a
12	chr1:72750124-72750174	MCF10A-Er-Src	breast:	n/a
13	chr1:72753076-72753126	ovcar-3	ovarian:	n/a
14	chr1:72748389-72748439	NH-A	brain:	n/a
15	chr1:72748139-72748189	AoSMC	blood vessel:	n/a
16	chr1:72750241-72750291	ProgFib	skin:	n/a
17	chr1:72749275-72749325	GM12892	blood:	n/a
18	chr1:72748610-72748660	HL-60	blood:	n/a
19	chr1:72748601-72748651	AG10803	skin:	n/a
20	chr1:72750502-72750552	NHDF-neo	bronchial:	n/a
21	chr1:72749275-72749325	IMR90	lung:	fetal
22	chr1:72748124-72748174	Hela-S3	cervix:	n/a
23	chr1:72748601-72748651	HEEpiC	esophagus:	n/a
24	chr1:72749581-72749631	SK-N-SH_RA	brain:	n/a
25	chr1:72749015-72749065	NHBE	bronchial:	n/a
26	chr1:72748139-72748189	LNCaP	prostate:	n/a
27	chr1:72749015-72749065	HIPEpiC	eye:	n/a
28	chr1:72748607-72748657	SK-N-SH	brain:	n/a
29	chr1:72750124-72750174	Caco-2	colon:	n/a
30	chr1:72750241-72750291	K562	blood:	n/a
31	chr1:72748610-72748660	HMEC	breast:	n/a
32	chr1:72749275-72749325	PFSK-1	brain:	n/a
33	chr1:72750241-72750291	NB4	blood:	n/a
34	chr1:72750241-72750291	GM06990	blood:	n/a
35	chr1:72750241-72750291	AG09309	skin:	n/a
36	chr1:72749880-72749930	SAEC	small airway:	n/a
37	chr1:72749064-72749114	HNPCEpiC	eye:	n/a
38	chr1:72749015-72749065	PrEC	prostate:	n/a
39	chr1:72749064-72749114	HRE	kidney:	n/a
40	chr1:72748607-72748657	MCF10A-Er-Src	breast:	n/a
41	chr1:72748607-72748657	HRE	kidney:	n/a
42	chr1:72749064-72749114	HepG2	liver:	n/a
43	chr1:72748139-72748189	NHBE	bronchial:	n/a
44	chr1:72749880-72749930	HCT-116	colon:	n/a
45	chr1:72749275-72749325	HCF	heart:	n/a
46	chr1:72749880-72749930	HEEpiC	esophagus:	n/a
47	chr1:72750124-72750174	HL-60	blood:	n/a
48	chr1:72749064-72749114	MCF10A-Er-Src	breast:	n/a
49	chr1:72750241-72750291	RPTEC	kidney:	n/a
50	chr1:72747802-72747852	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:
2	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
3	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:
4	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:

Variant related genes	Relation type
RPL31P12	TF binding region
NEGR1	TF binding region
GDI2P2	TF binding region
RPL31P12	CpG island
NEGR1	CpG island
GDI2P2	CpG island
ENSG00000139684	chromatin interactions

Extended variants
information (count: 5034 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:5034 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558778313	chr1:72603547-72603548	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs188662831	chr1:72603647-72603648	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs559591330	chr1:72603698-72603699	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs575028675	chr1:72603716-72603717	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs555670261	chr1:72603740-72603741	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs374034451	chr1:72603747-72603748	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs574355971	chr1:72603858-72603859	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs543337545	chr1:72603867-72603868	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs563324903	chr1:72603936-72603937	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs10218467	chr1:72603953-72603954	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146848827	chr1:72603987-72603988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs79917622	chr1:72604025-72604026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs180743929	chr1:72604070-72604071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs78872839	chr1:72604093-72604094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs112558566	chr1:72604097-72604098	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs567973241	chr1:72604104-72604105	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs140689618	chr1:72604124-72604125	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs192125543	chr1:72604146-72604147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs540961740	chr1:72604163-72604164	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs183891427	chr1:72604292-72604293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs559015325	chr1:72604301-72604302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs200915902	chr1:72604304-72604305	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs565811177	chr1:72604305-72604306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs74087163	chr1:72604327-72604328	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372874109	chr1:72604346-72604347	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs554378140	chr1:72604382-72604383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs552459416	chr1:72604384-72604385	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs574271508	chr1:72604402-72604403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs74887993	chr1:72604407-72604408	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs369301394	chr1:72604414-72604415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs556967892	chr1:72604482-72604483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs114846087	chr1:72604495-72604496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570836920	chr1:72604529-72604530	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs369663616	chr1:72604534-72604535	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs191539437	chr1:72604570-72604571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs545434979	chr1:72604582-72604583	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs559511752	chr1:72604612-72604613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528159348	chr1:72604624-72604625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11209917	chr1:72604678-72604679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373167609	chr1:72604692-72604693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561491931	chr1:72604744-72604745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530225980	chr1:72604778-72604779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188356870	chr1:72604780-72604781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192914136	chr1:72604782-72604783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs397785759	chr1:72604793-72604794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183151068	chr1:72604800-72604801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201488793	chr1:72604852-72604853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570208227	chr1:72604938-72604939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77435105	chr1:72604939-72604940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532563502	chr1:72604945-72604946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72602600-72604600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72604600-72629600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:72605600-72606400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:72605600-72606400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:72605800-72606200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:72605800-72606400	Enhancers	HUVEC	blood vessel
7	chr1:72606000-72606200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:72606000-72606400	Enhancers	HSMM	muscle
9	chr1:72606000-72606400	Enhancers	NHEK	skin
10	chr1:72606200-72613600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:72613600-72614200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:72614200-72624600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:72618600-72619000	Enhancers	Brain Substantia Nigra	brain
14	chr1:72629600-72630000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:72629600-72630000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:72630800-72633000	Enhancers	HUVEC	blood vessel
17	chr1:72633000-72636000	Weak transcription	HUVEC	blood vessel
18	chr1:72636000-72638600	Enhancers	HUVEC	blood vessel
19	chr1:72636600-72637000	Enhancers	Fetal Lung	lung
20	chr1:72642200-72642400	Enhancers	Colon Smooth Muscle	Colon
21	chr1:72642800-72643800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:72643400-72644200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:72643400-72644200	Enhancers	NHDF-Ad	bronchial
24	chr1:72643400-72644400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:72643400-72644400	Enhancers	Osteobl	bone
26	chr1:72643400-72644800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr1:72643600-72643800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:72643600-72644200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:72643600-72644200	Enhancers	HSMM	muscle
30	chr1:72643600-72644200	Enhancers	HSMMtube	muscle
31	chr1:72643600-72644400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:72643600-72644600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:72643600-72644600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:72643600-72645200	Enhancers	Rectal Smooth Muscle	rectum
35	chr1:72643800-72644200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:72643800-72644400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:72643800-72644400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:72643800-72644400	Enhancers	Colon Smooth Muscle	Colon
39	chr1:72644000-72644400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:72644200-72644600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:72644400-72644600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr1:72644400-72648800	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:72644400-72649000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:72644400-72649000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr1:72644400-72649200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:72644400-72649200	Weak transcription	Osteobl	bone
47	chr1:72644400-72668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:72644600-72648000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:72644600-72649200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:72644600-72649600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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