Variant report

Variant	esv1826553
Chromosome Location	chr1:72738721-72763358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:645)
CpG islands
(count:1100)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
13	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
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	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
19	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
20	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
21	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr1:72748405-72750930	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr1:72748399-72748786	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr1:72748477-72748773	A549	lung:	n/a	n/a
28	CREB1	chr1:72750306-72750765	GM12878	blood:	n/a	n/a
29	CTBP2	chr1:72747565-72750445	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:72750100-72750250	Caco-2	colon:	n/a	n/a
31	CTCF	chr1:72750180-72750330	WI-38	lung:	n/a	n/a
32	CTCF	chr1:72750040-72750190	AG10803	skin:	n/a	n/a
33	CTCF	chr1:72748100-72748250	HBMEC	blood vessel:	n/a	chr1:72748229-72748238 chr1:72748226-72748236
34	CTCF	chr1:72748180-72748330	HCFaa	heart:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
35	CTCF	chr1:72750860-72751010	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr1:72750000-72750150	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr1:72748340-72748490	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:72748002-72748073	Fibrobl	skin:	n/a	n/a
39	CTCF	chr1:72748460-72748610	AG04449	skin:	n/a	n/a
40	CTCF	chr1:72748420-72748570	AG09309	skin:	n/a	n/a
41	CTCF	chr1:72748120-72748270	HBMEC	blood vessel:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
42	CTCF	chr1:72750060-72750210	AG10803	skin:	n/a	n/a
43	CTCF	chr1:72750920-72751070	HCFaa	heart:	n/a	n/a
44	CTCF	chr1:72750120-72750270	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr1:72748480-72748630	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr1:72750040-72750190	GM12871	blood:	n/a	n/a
47	CTCF	chr1:72750860-72751010	BJ	skin:	n/a	n/a
48	CTCF	chr1:72748491-72748598	GM12878	blood:	n/a	n/a
49	CTCF	chr1:72748160-72748310	WERI-Rb-1	eye:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
50	CTCF	chr1:72748420-72748570	HBMEC	blood vessel:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72753076-72753126	GM19239	blood:	n/a
2	chr1:72749880-72749930	PANC-1	pancreas:	n/a
3	chr1:72753076-72753126	GM19239	blood:	n/a
4	chr1:72749880-72749930	PANC-1	pancreas:	n/a
5	chr1:72747802-72747852	K562	blood:	n/a
6	chr1:72748389-72748439	GM12892	blood:	n/a
7	chr1:72748389-72748439	MCF10A-Er-Src	breast:	n/a
8	chr1:72749735-72749785	BE2_C	brain:	n/a
9	chr1:72748389-72748439	AG04449	skin:	fetal
10	chr1:72750502-72750552	HAEpiC	amniotic membrane:	n/a
11	chr1:72750502-72750552	HEEpiC	esophagus:	n/a
12	chr1:72748389-72748439	HCM	heart:	n/a
13	chr1:72748139-72748189	HNPCEpiC	eye:	n/a
14	chr1:72749880-72749930	NT2-D1	testis:	n/a
15	chr1:72749275-72749325	HNPCEpiC	eye:	n/a
16	chr1:72749880-72749930	HCM	heart:	n/a
17	chr1:72750124-72750174	HIPEpiC	eye:	n/a
18	chr1:72748607-72748657	HEK293	kidney:	embryo
19	chr1:72750671-72750721	SKMC	muscle:	n/a
20	chr1:72749581-72749631	GM06990	blood:	n/a
21	chr1:72748607-72748657	BJ	skin:	n/a
22	chr1:72749064-72749114	PANC-1	pancreas:	n/a
23	chr1:72749275-72749325	AG09309	skin:	n/a
24	chr1:72748124-72748174	NHDF-neo	bronchial:	n/a
25	chr1:72750241-72750291	HCM	heart:	n/a
26	chr1:72749015-72749065	HCM	heart:	n/a
27	chr1:72749735-72749785	NHBE	bronchial:	n/a
28	chr1:72748607-72748657	HCT-116	colon:	n/a
29	chr1:72749880-72749930	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:72750671-72750721	K562	blood:	n/a
31	chr1:72750241-72750291	BJ	skin:	n/a
32	chr1:72749735-72749785	ECC-1	luminal epithelium:	n/a
33	chr1:72750241-72750291	HNPCEpiC	eye:	n/a
34	chr1:72750241-72750291	Jurkat	blood:	n/a
35	chr1:72748607-72748657	AoSMC	blood vessel:	n/a
36	chr1:72747802-72747852	HAEpiC	amniotic membrane:	n/a
37	chr1:72748389-72748439	HRCEpiC	kidney:	n/a
38	chr1:72749275-72749325	GM12892	blood:	n/a
39	chr1:72749064-72749114	CMK	blood:	n/a
40	chr1:72750671-72750721	LNCaP	prostate:	n/a
41	chr1:72748389-72748439	AG10803	skin:	n/a
42	chr1:72749064-72749114	ECC-1	luminal epithelium:	n/a
43	chr1:72748389-72748439	RPTEC	kidney:	n/a
44	chr1:72749581-72749631	RPTEC	kidney:	n/a
45	chr1:72753076-72753126	GM06990	blood:	n/a
46	chr1:72748607-72748657	AG04449	skin:	fetal
47	chr1:72750671-72750721	U87	brain:	n/a
48	chr1:72748610-72748660	HEEpiC	esophagus:	n/a
49	chr1:72748607-72748657	Jurkat	blood:	n/a
50	chr1:72749581-72749631	HRPEpiC	eye:	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: 738 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114944491	chr1:72738750-72738751	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs191206926	chr1:72738772-72738773	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs139660884	chr1:72738847-72738848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35729767	chr1:72738886-72738887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183459717	chr1:72738896-72738897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186768454	chr1:72738900-72738901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142936024	chr1:72738942-72738943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150733574	chr1:72738943-72738944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191572052	chr1:72738947-72738948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114742610	chr1:72738948-72738949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183292938	chr1:72738965-72738966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369418808	chr1:72738989-72738990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187968327	chr1:72739026-72739027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117955023	chr1:72739067-72739068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575725038	chr1:72739104-72739105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565721560	chr1:72739191-72739192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546410069	chr1:72739197-72739198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555068707	chr1:72739222-72739223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2051061	chr1:72739225-72739226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537253481	chr1:72739234-72739235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556873757	chr1:72739257-72739258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138290751	chr1:72739273-72739274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2051062	chr1:72739303-72739304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74088559	chr1:72739345-72739346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559415869	chr1:72739354-72739355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536522226	chr1:72739392-72739393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192010445	chr1:72739415-72739416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185199001	chr1:72739431-72739432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528541022	chr1:72739455-72739456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540383011	chr1:72739487-72739488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561828628	chr1:72739516-72739517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12737564	chr1:72739527-72739528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376245128	chr1:72739558-72739559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10493496	chr1:72739564-72739565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563724786	chr1:72739585-72739586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532704077	chr1:72739654-72739655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549119025	chr1:72739678-72739679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569953465	chr1:72739679-72739680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72942937	chr1:72739681-72739682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11383775	chr1:72739693-72739694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1130262	chr1:72739702-72739703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189663266	chr1:72739713-72739714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566005788	chr1:72739744-72739745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141987470	chr1:72739760-72739761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540568591	chr1:72739793-72739794	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192693272	chr1:72739795-72739796	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs568586537	chr1:72739839-72739840	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560488121	chr1:72739847-72739848	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537139446	chr1:72739857-72739858	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs557154061	chr1:72739899-72739900	Weak transcription	TF binding region	1 gene(s)	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:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72737600-72744200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72738000-72744200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:72738000-72745800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:72738200-72739000	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:72738400-72738800	Enhancers	Brain Germinal Matrix	brain
6	chr1:72738400-72739000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:72738600-72739200	Enhancers	Colon Smooth Muscle	Colon
8	chr1:72739000-72744400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr1:72739200-72741600	Weak transcription	Colon Smooth Muscle	Colon
10	chr1:72741600-72741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:72741600-72741800	Enhancers	Brain Angular Gyrus	brain
12	chr1:72741600-72741800	Enhancers	Colon Smooth Muscle	Colon
13	chr1:72741800-72742000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:72741800-72742200	Weak transcription	Colon Smooth Muscle	Colon
15	chr1:72741800-72742800	Weak transcription	Brain Angular Gyrus	brain
16	chr1:72742200-72744000	Enhancers	Colon Smooth Muscle	Colon
17	chr1:72742400-72742600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:72742600-72742800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr1:72742600-72742800	Enhancers	Brain Substantia Nigra	brain
20	chr1:72742600-72743000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:72742800-72743000	Enhancers	Brain Angular Gyrus	brain
22	chr1:72742800-72743000	Enhancers	Brain Cingulate Gyrus	brain
23	chr1:72742800-72743200	Enhancers	Dnd41	blood
24	chr1:72742800-72744000	Weak transcription	Brain Substantia Nigra	brain
25	chr1:72742800-72745800	Weak transcription	Brain Anterior Caudate	brain
26	chr1:72743000-72745000	Weak transcription	Brain Angular Gyrus	brain
27	chr1:72743000-72745000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:72743000-72745800	Weak transcription	Brain Cingulate Gyrus	brain
29	chr1:72743200-72743600	Weak transcription	Dnd41	blood
30	chr1:72743600-72745800	Enhancers	Dnd41	blood
31	chr1:72743800-72744200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr1:72744000-72744200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr1:72744000-72745000	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:72744000-72745200	Enhancers	Brain Substantia Nigra	brain
36	chr1:72744200-72744400	Enhancers	NHDF-Ad	bronchial
37	chr1:72744200-72744600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr1:72744200-72744800	Active TSS	Stomach Smooth Muscle	stomach
39	chr1:72744200-72744800	Enhancers	HUVEC	blood vessel
40	chr1:72744200-72745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:72744200-72745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:72744200-72746000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:72744400-72744600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:72744400-72745000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:72744400-72745800	Weak transcription	NHDF-Ad	bronchial
46	chr1:72744400-72746400	Enhancers	Rectal Smooth Muscle	rectum
47	chr1:72744600-72744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:72744600-72745200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:72744600-72745600	Enhancers	Osteobl	bone
50	chr1:72744600-72745800	Enhancers	Pancreatic Islets	Pancreatic Islet

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