Variant report

Variant	nsv1008754
Chromosome Location	chr1:72733738-72763358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:1099)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
2	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
3	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
11	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
13	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
16	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
18	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
21	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:72748405-72750930	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr1:72750306-72750765	GM12878	blood:	n/a	n/a
27	CREB1	chr1:72748477-72748773	A549	lung:	n/a	n/a
28	CREB1	chr1:72748399-72748786	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr1:72747565-72750445	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:72748340-72748490	BJ	skin:	n/a	n/a
31	CTCF	chr1:72748120-72748390	NHEK	skin:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
32	CTCF	chr1:72752254-72752336	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:72750900-72751050	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr1:72750180-72750330	WI-38	lung:	n/a	n/a
35	CTCF	chr1:72748180-72748330	HCFaa	heart:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
36	CTCF	chr1:72750080-72750230	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:72748340-72748490	GM06990	blood:	n/a	n/a
38	CTCF	chr1:72750060-72750210	HMF	breast:	n/a	n/a
39	CTCF	chr1:72750120-72750270	HCFaa	heart:	n/a	n/a
40	CTCF	chr1:72748420-72748570	AG09319	gingival:	n/a	n/a
41	CTCF	chr1:72748320-72748470	HMF	breast:	n/a	n/a
42	CTCF	chr1:72748340-72748490	HMEC	breast:	n/a	n/a
43	CTCF	chr1:72749080-72749230	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr1:72748380-72748530	AG10803	skin:	n/a	n/a
45	CTCF	chr1:72750096-72750259	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:72750060-72750210	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr1:72748360-72748510	HVMF	connective:	n/a	n/a
48	CTCF	chr1:72746480-72746630	AG04449	skin:	n/a	n/a
49	CTCF	chr1:72748240-72748390	HepG2	liver:	n/a	chr1:72748257-72748267
50	CTCF	chr1:72748420-72748570	AoAF	blood vessel:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72749064-72749114	GM19239	blood:	n/a
2	chr1:72749064-72749114	GM19239	blood:	n/a
3	chr1:72753076-72753126	U87	brain:	n/a
4	chr1:72747802-72747852	U87	brain:	n/a
5	chr1:72750241-72750291	A549	lung:	n/a
6	chr1:72748139-72748189	H1-hESC	embryonic stem cell:	embryo
7	chr1:72749015-72749065	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:72749275-72749325	NHBE	bronchial:	n/a
9	chr1:72750241-72750291	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:72748610-72748660	HepG2	liver:	n/a
11	chr1:72748389-72748439	Jurkat	blood:	n/a
12	chr1:72748139-72748189	HCM	heart:	n/a
13	chr1:72750124-72750174	AG09319	gingival:	n/a
14	chr1:72748389-72748439	CMK	blood:	n/a
15	chr1:72749581-72749631	BE2_C	brain:	n/a
16	chr1:72748139-72748189	NB4	blood:	n/a
17	chr1:72750124-72750174	LNCaP	prostate:	n/a
18	chr1:72748607-72748657	HEEpiC	esophagus:	n/a
19	chr1:72748139-72748189	BJ	skin:	n/a
20	chr1:72749064-72749114	HL-60	blood:	n/a
21	chr1:72748139-72748189	HNPCEpiC	eye:	n/a
22	chr1:72749064-72749114	CMK	blood:	n/a
23	chr1:72747802-72747852	ovcar-3	ovarian:	n/a
24	chr1:72748607-72748657	GM12892	blood:	n/a
25	chr1:72749015-72749065	NB4	blood:	n/a
26	chr1:72748610-72748660	AG09319	gingival:	n/a
27	chr1:72749015-72749065	HUVEC	blood vessel:	n/a
28	chr1:72749015-72749065	HRCEpiC	kidney:	n/a
29	chr1:72749581-72749631	GM06990	blood:	n/a
30	chr1:72749581-72749631	A549	lung:	n/a
31	chr1:72749581-72749631	HCT-116	colon:	n/a
32	chr1:72749064-72749114	HEEpiC	esophagus:	n/a
33	chr1:72749015-72749065	CMK	blood:	n/a
34	chr1:72749581-72749631	HL-60	blood:	n/a
35	chr1:72750124-72750174	MCF-7	breast:	n/a
36	chr1:72748139-72748189	GM12891	blood:	n/a
37	chr1:72749064-72749114	HNPCEpiC	eye:	n/a
38	chr1:72749880-72749930	HCPEpiC	choroid plexus:	n/a
39	chr1:72750502-72750552	HEEpiC	esophagus:	n/a
40	chr1:72750241-72750291	HL-60	blood:	n/a
41	chr1:72748610-72748660	BE2_C	brain:	n/a
42	chr1:72749735-72749785	HL-60	blood:	n/a
43	chr1:72749064-72749114	AG04450	lung:	fetal
44	chr1:72748601-72748651	GM12878	blood:	n/a
45	chr1:72748601-72748651	PFSK-1	brain:	n/a
46	chr1:72748389-72748439	ECC-1	luminal epithelium:	n/a
47	chr1:72748139-72748189	IMR90	lung:	fetal
48	chr1:72748607-72748657	K562	blood:	n/a
49	chr1:72750124-72750174	BE2_C	brain:	n/a
50	chr1:72750241-72750291	K562	blood:	n/a

(count:3 , 50 per page) page: 1

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

No data

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: 914 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187237521	chr1:72733746-72733747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552741228	chr1:72733790-72733791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533486094	chr1:72733795-72733796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544758995	chr1:72733818-72733819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1380995	chr1:72733841-72733842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs72942922	chr1:72733855-72733856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548451489	chr1:72733857-72733858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568385401	chr1:72733880-72733881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537467707	chr1:72733930-72733931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72942924	chr1:72733977-72733978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116520641	chr1:72734002-72734003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539545090	chr1:72734004-72734005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553242543	chr1:72734017-72734018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114051547	chr1:72734060-72734061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535779764	chr1:72734108-72734109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555724059	chr1:72734170-72734171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190925628	chr1:72734202-72734203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150685254	chr1:72734221-72734222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182718481	chr1:72734252-72734253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187356000	chr1:72734256-72734257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539150985	chr1:72734264-72734265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539924546	chr1:72734280-72734281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17097679	chr1:72734323-72734324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13375319	chr1:72734379-72734380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs557880829	chr1:72734393-72734394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562051474	chr1:72734396-72734397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531063178	chr1:72734425-72734426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572730545	chr1:72734446-72734447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550997426	chr1:72734496-72734497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12727565	chr1:72734514-72734515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190657434	chr1:72734543-72734544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149563621	chr1:72734584-72734585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58064544	chr1:72734587-72734588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377470013	chr1:72734603-72734604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182455399	chr1:72734608-72734609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547095712	chr1:72734637-72734638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187721863	chr1:72734638-72734639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535663967	chr1:72734678-72734679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555561337	chr1:72734697-72734698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188068497	chr1:72734740-72734741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537746894	chr1:72734912-72734913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552570712	chr1:72734954-72734955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540259170	chr1:72735022-72735023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375832426	chr1:72735030-72735031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577544004	chr1:72735077-72735078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572578743	chr1:72735102-72735103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539814536	chr1:72735118-72735119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553464653	chr1:72735153-72735154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573360269	chr1:72735158-72735159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542020496	chr1:72735247-72735248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
small cell lung cancer	20016488	CNVD

Chromatin state (count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72713800-72735600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72728400-72738600	Weak transcription	Colon Smooth Muscle	Colon
3	chr1:72735600-72737600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:72737600-72744200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:72738000-72744200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:72738000-72745800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:72738200-72739000	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:72738400-72738800	Enhancers	Brain Germinal Matrix	brain
9	chr1:72738400-72739000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:72738600-72739200	Enhancers	Colon Smooth Muscle	Colon
11	chr1:72739000-72744400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:72739200-72741600	Weak transcription	Colon Smooth Muscle	Colon
13	chr1:72741600-72741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:72741600-72741800	Enhancers	Brain Angular Gyrus	brain
15	chr1:72741600-72741800	Enhancers	Colon Smooth Muscle	Colon
16	chr1:72741800-72742000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:72741800-72742200	Weak transcription	Colon Smooth Muscle	Colon
18	chr1:72741800-72742800	Weak transcription	Brain Angular Gyrus	brain
19	chr1:72742200-72744000	Enhancers	Colon Smooth Muscle	Colon
20	chr1:72742400-72742600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:72742600-72742800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr1:72742600-72742800	Enhancers	Brain Substantia Nigra	brain
23	chr1:72742600-72743000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:72742800-72743000	Enhancers	Brain Angular Gyrus	brain
25	chr1:72742800-72743000	Enhancers	Brain Cingulate Gyrus	brain
26	chr1:72742800-72743200	Enhancers	Dnd41	blood
27	chr1:72742800-72744000	Weak transcription	Brain Substantia Nigra	brain
28	chr1:72742800-72745800	Weak transcription	Brain Anterior Caudate	brain
29	chr1:72743000-72745000	Weak transcription	Brain Angular Gyrus	brain
30	chr1:72743000-72745000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr1:72743000-72745800	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:72743200-72743600	Weak transcription	Dnd41	blood
33	chr1:72743600-72745800	Enhancers	Dnd41	blood
34	chr1:72743800-72744200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr1:72744000-72744200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:72744000-72745000	Weak transcription	Colon Smooth Muscle	Colon
38	chr1:72744000-72745200	Enhancers	Brain Substantia Nigra	brain
39	chr1:72744200-72744400	Enhancers	NHDF-Ad	bronchial
40	chr1:72744200-72744600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr1:72744200-72744800	Active TSS	Stomach Smooth Muscle	stomach
42	chr1:72744200-72744800	Enhancers	HUVEC	blood vessel
43	chr1:72744200-72745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:72744200-72745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:72744200-72746000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:72744400-72744600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:72744400-72745000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr1:72744400-72745800	Weak transcription	NHDF-Ad	bronchial
49	chr1:72744400-72746400	Enhancers	Rectal Smooth Muscle	rectum
50	chr1:72744600-72744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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