Variant report

Variant	nsv830192
Chromosome Location	chr1:72616562-72806118
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	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
5	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
6	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
7	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
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	chr1:72707115-72707480	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:72731625-72731886	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:72731623-72731775	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
21	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
22	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:72707115-72707489	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
25	CEBPB	chr1:72707157-72707388	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
29	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
31	CEBPB	chr1:72707179-72707470	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:72707185-72707435	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
40	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
43	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
44	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
46	CEBPB	chr1:72707117-72707455	A549	lung:	n/a	n/a
47	CEBPD	chr1:72707177-72707369	HepG2	liver:	n/a	n/a
48	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72748607-72748657	AG10803	skin:	n/a
2	chr1:72749735-72749785	HUVEC	blood vessel:	n/a
3	chr1:72749015-72749065	HepG2	liver:	n/a
4	chr1:72748607-72748657	AG10803	skin:	n/a
5	chr1:72749735-72749785	HUVEC	blood vessel:	n/a
6	chr1:72749015-72749065	HepG2	liver:	n/a
7	chr1:72748601-72748651	HNPCEpiC	eye:	n/a
8	chr1:72750671-72750721	SK-N-MC	brain:	n/a
9	chr1:72750671-72750721	SKMC	muscle:	n/a
10	chr1:72749581-72749631	HEK293	kidney:	embryo
11	chr1:72749275-72749325	HCT-116	colon:	n/a
12	chr1:72748601-72748651	HRE	kidney:	n/a
13	chr1:72749275-72749325	MCF-7	breast:	n/a
14	chr1:72749015-72749065	NB4	blood:	n/a
15	chr1:72750241-72750291	BE2_C	brain:	n/a
16	chr1:72748610-72748660	AG04449	skin:	fetal
17	chr1:72749735-72749785	Hela-S3	cervix:	n/a
18	chr1:72747802-72747852	GM06990	blood:	n/a
19	chr1:72749064-72749114	HepG2	liver:	n/a
20	chr1:72749735-72749785	AG04450	lung:	fetal
21	chr1:72749275-72749325	PFSK-1	brain:	n/a
22	chr1:72748607-72748657	NT2-D1	testis:	n/a
23	chr1:72749735-72749785	GM19239	blood:	n/a
24	chr1:72749064-72749114	HUVEC	blood vessel:	n/a
25	chr1:72753076-72753126	HCM	heart:	n/a
26	chr1:72749735-72749785	GM12878	blood:	n/a
27	chr1:72753076-72753126	NB4	blood:	n/a
28	chr1:72749064-72749114	HRPEpiC	eye:	n/a
29	chr1:72749015-72749065	AG09309	skin:	n/a
30	chr1:72750124-72750174	NB4	blood:	n/a
31	chr1:72748139-72748189	HEK293	kidney:	embryo
32	chr1:72750502-72750552	Hela-S3	cervix:	n/a
33	chr1:72750502-72750552	AG04450	lung:	fetal
34	chr1:72749735-72749785	SAEC	small airway:	n/a
35	chr1:72748124-72748174	HCT-116	colon:	n/a
36	chr1:72753076-72753126	ProgFib	skin:	n/a
37	chr1:72749015-72749065	GM19239	blood:	n/a
38	chr1:72750671-72750721	IMR90	lung:	fetal
39	chr1:72750502-72750552	HEEpiC	esophagus:	n/a
40	chr1:72750241-72750291	Hepatocyte	liver:	n/a
41	chr1:72748124-72748174	A549	lung:	n/a
42	chr1:72750241-72750291	GM12892	blood:	n/a
43	chr1:72750124-72750174	AG04450	lung:	fetal
44	chr1:72748607-72748657	RPTEC	kidney:	n/a
45	chr1:72749880-72749930	K562	blood:	n/a
46	chr1:72749015-72749065	MCF-7	breast:	n/a
47	chr1:72748601-72748651	AG09319	gingival:	n/a
48	chr1:72749064-72749114	HCF	heart:	n/a
49	chr1:72749275-72749325	SAEC	small airway:	n/a
50	chr1:72748607-72748657	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:
2	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:
3	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
4	chr1:72752065..72752600-chr8:87527466..87528155,2	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: 4604 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4604 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547506609	chr1:72616617-72616618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369560552	chr1:72616653-72616654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144153243	chr1:72616659-72616660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536391419	chr1:72616671-72616672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs36041772	chr1:72616674-72616675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547347858	chr1:72616698-72616699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549851947	chr1:72616707-72616708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569522913	chr1:72616715-72616716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183296663	chr1:72616751-72616752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558447453	chr1:72616768-72616769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs57857000	chr1:72616783-72616784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573577705	chr1:72616784-72616785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534897299	chr1:72616791-72616792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188688199	chr1:72616809-72616810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192529019	chr1:72616820-72616821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574366816	chr1:72616955-72616956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556046887	chr1:72616988-72616989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543554090	chr1:72617042-72617043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147774062	chr1:72617043-72617044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576733705	chr1:72617083-72617084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372980672	chr1:72617117-72617118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577719467	chr1:72617124-72617125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565458166	chr1:72617199-72617200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12088565	chr1:72617285-72617286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140133889	chr1:72617311-72617312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561165110	chr1:72617331-72617332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1385922	chr1:72617333-72617334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549864254	chr1:72617342-72617343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544921520	chr1:72617388-72617389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569787230	chr1:72617418-72617419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538731526	chr1:72617419-72617420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77814791	chr1:72617476-72617477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565865476	chr1:72617552-72617553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534652337	chr1:72617643-72617644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553821327	chr1:72617702-72617703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554810085	chr1:72617733-72617734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6424458	chr1:72617740-72617741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572076859	chr1:72617761-72617762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369996335	chr1:72617790-72617791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542620571	chr1:72617800-72617801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577044574	chr1:72617810-72617811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545890877	chr1:72617865-72617866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112547783	chr1:72617866-72617867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560836506	chr1:72617895-72617896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572589613	chr1:72617897-72617898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72682725	chr1:72617939-72617940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561580002	chr1:72617946-72617947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530057399	chr1:72618005-72618006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544881340	chr1:72618009-72618010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375079700	chr1:72618010-72618011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

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

Chromatin state (count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72604600-72629600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72614200-72624600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:72618600-72619000	Enhancers	Brain Substantia Nigra	brain
4	chr1:72629600-72630000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:72629600-72630000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:72630800-72633000	Enhancers	HUVEC	blood vessel
7	chr1:72633000-72636000	Weak transcription	HUVEC	blood vessel
8	chr1:72636000-72638600	Enhancers	HUVEC	blood vessel
9	chr1:72636600-72637000	Enhancers	Fetal Lung	lung
10	chr1:72642200-72642400	Enhancers	Colon Smooth Muscle	Colon
11	chr1:72642800-72643800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:72643400-72644200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:72643400-72644200	Enhancers	NHDF-Ad	bronchial
14	chr1:72643400-72644400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr1:72643400-72644400	Enhancers	Osteobl	bone
16	chr1:72643400-72644800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr1:72643600-72643800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:72643600-72644200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:72643600-72644200	Enhancers	HSMM	muscle
20	chr1:72643600-72644200	Enhancers	HSMMtube	muscle
21	chr1:72643600-72644400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:72643600-72644600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:72643600-72644600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:72643600-72645200	Enhancers	Rectal Smooth Muscle	rectum
25	chr1:72643800-72644200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:72643800-72644400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:72643800-72644400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:72643800-72644400	Enhancers	Colon Smooth Muscle	Colon
29	chr1:72644000-72644400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:72644200-72644600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:72644400-72644600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:72644400-72648800	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:72644400-72649000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:72644400-72649000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr1:72644400-72649200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:72644400-72649200	Weak transcription	Osteobl	bone
37	chr1:72644400-72668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:72644600-72648000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:72644600-72649200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:72644600-72649600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:72644600-72649800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:72644600-72649800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:72644800-72648800	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr1:72645200-72649200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr1:72646400-72647000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:72647000-72647200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:72647200-72648800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:72647800-72648000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:72648000-72648200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:72648000-72648200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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